684
80
5
5
87
Cat. No. | Product Name | ||
---|---|---|---|
L4510 | 抗寄生虫库 | 419 compounds | |
419 种具有抗寄生虫活性的小分子化合物; | |||
L6620 | 抗寄生虫天然产物库 | 253 compounds | |
253 个抗寄生虫相关的天然产物集合,是药物开发、药理研究的有效工具; | |||
DF4500 | 多样性核心库Part1 | 50000 compounds | |
绝大部分分子量<500,主要集中于250-450之间,方便后续的改造优化; | |||
VM1400 | 多样性核心库Part2 | 25920 compounds | |
分子量<500,主要集中于250-450之间,方便后续的改造优化; | |||
L9830 | 抗帕金森病化合物库 | 857 compounds | |
857 种帕金森病相关的化合物集合,可用于高通量和高内涵筛选; |
Cat. No. | Product Name | Form | Specificity Of Inhibition |
---|---|---|---|
CL0124 |
AMPAR antagonist/activator kit
AMPAR antagonist/activator kit |
||
CL0093 |
PARP inhibitor kit
PARP inhibitor kit |
||
CL0050 |
Antiparasitic compound kit
Antiparasitic compound kit |
||
C0113 |
Magrose Beads Heparin
肝素磁珠 |
||
CL0076 |
PPAR inhibitor/activator kit
PPAR inhibitor/activator kit |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1065 |
PAR-4 Agonist Peptide, amide TFA
PAR-4-AP (TFA),AY-NH2 (TFA) |
Protease-activated Receptor | GPCR/G Protein |
PAR-4 Agonist Peptide, amide TFA (PAR-4-AP (TFA)) 是一种蛋白酶激活受体 4 (PAR-4) 激动剂,对 PAR-1 或 PAR-2 均无影响,其作用可被 PAR-4 拮抗剂阻断。 | |||
TP1046L |
PAR-2 Activating Peptide acetate
SLIGRL-NH2 acetate,PAR-2 Activating Peptide acetate(171436-38-7 free base),Protease-Activated Receptor-2 Activating Peptide acetate |
Protease-activated Receptor | GPCR/G Protein |
PAR-2 Activating Peptide acetate (SLIGRL-NH2 acetate)(171436-38-7 free base) 是 Protease-Activated Receptor-2 (PAR-2) 的激动剂。 | |||
T8917 |
PAR-2-IN-1
IUN76750,8-(叔丁基)-6-氯咪唑并[1,2-B]吡啶-2-羧酸甲酯 |
Protease-activated Receptor | GPCR/G Protein |
PAR-2-IN-1 (IUN76750) 是一种 PAR-2 信号通路抑制剂,具有抗炎和抗癌作用。 | |||
T38836L |
Protease-Activated Receptor-1, PAR-1 Agonist acetate
|
Protease-activated Receptor | GPCR/G Protein |
Protease-Activated Receptor-1, PAR-1 Agonist acetate 是一种选择性蛋白酶激活受体 1 (PAR-1) 激动剂肽。 它对应于 PAR1 栓系配体,可以选择性地模拟凝血酶通过该受体的作用。 | |||
T7623 |
PAR-4 Agonist Peptide, amide
AY-NH2,PAR-4 Agonist Peptide, amide(2TFA),PAR-4-AP |
Protease-activated Receptor | GPCR/G Protein |
PAR-4 Agonist Peptide, amide (AY-NH2) 是蛋白酶激活受体 4 (PAR-4) 的激动剂,对 PAR-1 或 PAR-2 均无影响,其作用可被 PAR-4 拮抗剂阻断。 | |||
T36293 |
PAR 4 (1-6)
|
||
PAR 4 (1-6) 可用于生命科学领域的相关研究。其产品编号为 T36293,CAS号为 225779-44-2。 | |||
T7625 |
TRAP-6
PAR-1 agonist peptide,Thrombin Receptor Activator Peptide 6,TRAP-6(2TFA) |
Protease-activated Receptor | GPCR/G Protein |
TRAP-6 (Thrombin Receptor Activator Peptide 6) 是一种多肽片段,是选择性的蛋白酶激活受体 1 (PAR1) 激动剂,通过凝血酶受体激活人血小板。 | |||
T7623L |
PAR-4 Agonist Peptide, amide acetate
PAR-4 Agonist Peptide, amide acetate(352017-71-1 free base) |
Protease-activated Receptor | GPCR/G Protein |
PAR-4 Agonist Peptide, amide acetate 是蛋白酶激活受体 4 (PAR-4) 的激动剂。 | |||
T38836 |
Protease-Activated Receptor-1, PAR-1 Agonist
|
||
Protease-Activated Receptor-1 (PAR-1) Agonist, a selective peptide, activates the PAR-1 receptor by mimicking the specific actions of thrombin. It corresponds to the PAR1 tethered ligand, facilitating selective activation of this receptor. | |||
T36286 |
Protease-Activated Receptor-3 (PAR-3) (1-6), human
|
||
TFRGAP-amide, human PAR-3-derived tethered ligand sequence which does not activate PAR-3 but rather activates PAR-1 and PAR-2, either in Jurkat or in other PAR-expressing cells. | |||
T36288 |
Protease-Activated Receptor-1, PAR-1 Agonist TFA
|
||
Protease-Activated Receptor-1 (PAR-1) Agonist TFA is a selective peptide that acts as an agonist for the proteinase-activated receptor-1 (PAR-1). Corresponding to the tethered ligand of PAR-1, this compound mimics the actions of thrombin through the PAR-1 receptor[1][2]. | |||
T36289 |
Protease-Activated Receptor-3 (PAR-3) (1-6), human TFA
|
||
Protease-Activated Receptor-3 (PAR-3) (1-6), human TFA is a peptide that acts as an agonist for the proteinase-activated receptor (PAR-3)[1]. | |||
TP1046 |
SLIGRL-NH2
Protease-Activated Receptor-2 Activating Peptide |
Protease-activated Receptor | GPCR/G Protein |
SLIGRL-NH2 (Protease-Activated Receptor-2 Activating Peptide) 为一种蛋白酶激活受体-2 (PAR-2) 激动剂,具有诱导非组胺能性瘙痒的功能。 | |||
T36531 |
PAR2 (1-6) (mouse, rat)
PAR2 (1-6) (mouse, rat) |
||
PAR2 (1-6) is a synthetic peptide agonist of proteinase-activated receptor 2 (PAR2) that corresponds to residues 1-6 of the amino terminal tethered ligand sequence of mouse and rat PAR2. It also corresponds to residues 39-44 and 37-42 of the mouse and rat full-length sequences, respectively. PAR2 (1-6) induces relaxation in precontracted rat arteries in a concentration-dependent manner, an effect that can be reduced by the nitric oxide synthase inhibitor L-NNA . It inhibits keratinocyte growth i... | |||
T76650 |
PAR-2 (1-6) (human)
|
||
PAR-2 (1-6) (human) (SLIGKV) 是 PAR-2的多肽激动剂。 | |||
T75904 |
PAR 4 (1-6) (TFA)
|
||
GYPGQV TFA (PAR 4 (1-6) TFA) 是一种六肽,作为蛋白酶激活受体 4 (PAR4) 片段,能特异性抑制PAR4。 | |||
T35955 |
PAR2 (1-6) amide (human) (trifluoroacetate salt)
PAR2 (1-6) amide (human) (trifluoroacetate salt) |
||
PAR2 (1-6) amide is a synthetic peptide agonist of proteinase-activated receptor 2 (PAR2) that corresponds to residues 1-6 of the amino terminal tethered ligand sequence of human PAR2 and residues 37-42 of the full-length sequence.1It binds to NCTC 2544 cells expressing human PAR2 (Ki= 9.64 μM in a radioligand binding assay) and induces calcium mobilization in the same cells (EC50= 0.075 μM).2PAR2 (1-6) amide (100 μM) reduces colony formation of A549 lung cancer cells.1It induces superoxide prod... | |||
T23189 | prostate apoptosis response protein PAR-4 (2-7) [Homo sapiens] | Others | Others |
Prostate apoptosis response protein PAR-4 (2-7) [Homo sapiens] is a peptide with the sequence H2N-Ala-Thr-Gly-Gly-Tyr-Arg-OH, MW= 623.66. | |||
T7137 |
I-191
|
Protease-activated Receptor | GPCR/G Protein |
I-191 是选择性有效的蛋白酶激活受体 2 拮抗剂。 | |||
TQ0012 |
AZ3451
|
Protease-activated Receptor | GPCR/G Protein |
AZ3451 是蛋白酶激活受体 2 的变构拮抗剂,IC50值为 23 nM。 | |||
T1986 |
Atopaxar
E5555,ER-172594-00 |
Protease-activated Receptor | GPCR/G Protein |
Atopaxar (E5555) 是一种高效、可口服的,选择性的,可逆的凝血酶受体蛋白酶激活受体-1 (PAR-1) 拮抗剂。它是一种抗血小板剂,能干扰血小板信号,可用于动脉粥样硬化血栓性疾病的研究。 | |||
T2370 |
AC-55541
AOB2796 |
Proteasome; Protease-activated Receptor | GPCR/G Protein; Proteases/Proteasome; Ubiquitination |
AC-55541 (AOB2796) 是高选择性的蛋白酶激活受体 2(PAR2)激动剂,pEC50为6.7。它在 PI 水解测定和 Ca2+动态测定中的pEC50值为 5.9 和 6.6,在体内表现出伤害感受器活性。 | |||
T1893 |
Parmodulin 2
ML 161 |
Protease-activated Receptor | GPCR/G Protein |
Parmodulin 2 (ML 161) 是一种蛋白酶激活受体 1(PAR1) 变构抑制剂,IC50为 0.26 μM。它是蛋白酶激活受体 1 (PAR1) 介导的血小板活化的抑制剂,可以抑制体外血小板聚集和体内血小板血栓形成。 | |||
T7013 |
Vorapaxar
SCH 530348,MK-5348,沃拉帕沙 |
Protease-activated Receptor | GPCR/G Protein |
Vorapaxar (MK-5348) 是抗血小板药物,是一种选择性、口服活性和竞争性的凝血酶受体蛋白酶激活受体(PAR-1)拮抗剂,Ki 值为 8.1 nM。它靠剂量依赖性抑制凝血酶受体激活肽 (TRAP) 诱导的血小板聚集。 | |||
T6912 |
NU1025
NSC 696807 |
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
NU1025 (NSC-696807) 是一种PARP 的有效抑制剂,IC50为 400 nM,Ki 为 48 nM。它可增强电离辐射和抗癌药物的细胞毒性,有抗癌和神经保护的作用。 | |||
T3098 |
Vorapaxar sulfate
SCH 530348 sulfate,Zontivity,vorapaxar monosulfate,沃拉帕沙 |
Protease-activated Receptor | GPCR/G Protein |
Vorapaxar sulfate (Zontivity) 是一种选择性、口服活性和竞争性的凝血酶受体蛋白酶激活受体(PAR-1)拮抗剂,Ki 值为 8.1 nM。它剂量依赖性抑制凝血酶受体激活肽 (TRAP) 诱导的血小板聚集,是抗血小板药物。 | |||
T0948 |
Adrenalone hydrochloride
Adrenalone HCl,肾上腺酮盐酸盐,盐酸肾上腺酮 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Adrenalone hydrochloride (Adrenalone HCl) 是一种多巴胺β氧化酶 (dopamine β oxidase) 抑制剂,结构与去甲肾上腺素转运蛋白 (NET) 配体相似,IC50=36.9 μM。它是一种肾上腺素能 (adrenergic) 激动剂,用作局部血管收缩剂和止血剂。 | |||
T12870 |
SCH79797 dihydrochloride
|
Apoptosis; Others; Protease-activated Receptor | Apoptosis; GPCR/G Protein; Others |
SCH79797 dihydrochloride 是一种有效的特异性蛋白酶激活受体 1 (PAR1) 拮抗剂,IC50 为 70 nM,Ki 为 35 nM。SCH79797 dihydrochloride 具有抗增殖和促凋亡作用。 | |||
T1986L |
Atopaxar Hydrobromide
|
Protease-activated Receptor | GPCR/G Protein |
Atopaxar hydrobromide 是可口服的,高效选择性的可逆凝血酶受体蛋白酶激活受体-1 拮抗剂。它是一种抗血小板剂,能干扰血小板信号,用于动脉粥样硬化血栓性疾病的研究。 | |||
T7513 |
Protease-Activated Receptor-2, amide
蛋白酶活化的受体-2,酰胺,SLIGKV-NH2,H-丝氨酰亮氨酰异亮氨酰甘氨酰赖氨酰缬氨酰NH2 |
Protease-activated Receptor | GPCR/G Protein |
Protease-Activated Receptor-2, amide (SLIGKV-NH2) 是 PAR2 的激动剂,IC50为 10.4 M。 | |||
T4186 |
AC-264613
AC264613 |
Protease-activated Receptor | GPCR/G Protein |
AC-264613 是一种选择性蛋白酶激活受体 (PAR-2) 激动剂,pEC50为 7.5。 | |||
T7380 |
Protease-Activated Receptor-4
蛋白酶活化的受体-4 |
Protease-activated Receptor | GPCR/G Protein |
Protease-Activated Receptor-4 是蛋白酶激活受体 4 激动剂,具有抗血小板治疗。 | |||
T7573 |
TFLLR-NH2
TFLLR-NH2(2TFA) |
Protease-activated Receptor | GPCR/G Protein |
TFLLR-NH2 是选择性的一种PAR1激动剂,EC50值为1.9 μM。 | |||
T28281 |
OXSI-2
OXSI 2,Syk Inhibitor |
Syk | Angiogenesis; Tyrosine Kinase/Adaptors |
OXSI-2 (Syk Inhibitor) 是 Syk 的抑制剂,EC50 为 313 nM,IC50 为 14 nM。 OXSI-2 完全抑制适配器蛋白 LAT Y191 磷酸化和 Syk 介导的血小板聚集。 | |||
T7496 |
Thrombin Receptor Activator for Peptide 5 (TRAP-5)
Thrombin Receptor Activator for Peptide |
Protease-activated Receptor | GPCR/G Protein |
Thrombin Receptor Activator for Peptide 5 (TRAP-5) 也称为凝血因子 II 受体 (1-5) 或蛋白酶激活受体 1 (1-5),用于研究冠心病 (CHD)。 | |||
T38079 |
DL-Propargylglycine HCl
DL-Propargyl Glycine HCl,DL-Propargyl Glycine hydrochloride |
Others | Others |
DL-Propargylglycine HCl (DL-Propargyl Glycine HCl)是一种有效的胱硫氨酸 γ-裂解酶的不可逆抑制剂,可用于研究心力衰竭。 | |||
T20129 |
L-Propargylglycine
(S)-Propargylglycine,(S)-alpha.Propargylglycine,Propargylglycine,L-炔丙基甘氨酸 |
Others | Others |
L-Propargylglycine ((S)-Propargylglycine) 是一种脯氨酸酶抑制剂。 | |||
T78182 |
PARP-1-IN-4
|
Others; PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair; Others |
PARP-1-IN-4 是一种有效的 PARP-1抑制剂,具有潜在的看抗肿瘤活性,抑制 PARP-1 可用于癌症的发生。 | |||
T66154 |
Paroxypropione
|
||
It is an inhibitor of the Human Apurinic/apyrimidinic Endonuclease 1 (APE1) | |||
TQ0200 |
Paricalcitol
|
||
Paricalcitol 是一种 vitamin D receptor 激活剂,是一种 vitamin D 类似物,用于研究继发性甲状旁腺功能亢进,该疾病与慢性肾功能衰竭有关。 | |||
T22323 |
Enoxaparin sodium
|
Thrombin | Proteases/Proteasome |
Enoxaparin sodium 是一种低分子量肝素 (LMWH),已获得美国 FDA 批准,可用于医疗管理的 ST 段心肌梗死 (STEMI) 或 STEMI 及随后的经皮冠状动脉介入治疗 (PCI) 患者。它与抗凝血酶结合并增强其作用,并抑制凝血因子 XIa、IXa、Xa 和 IIa(凝血酶),从而防止血栓形成。 | |||
T5686 |
Isopropylparaben
|
Others | Others |
Isopropylparaben 是一种防腐剂和防腐杀虫剂。 | |||
T18831 |
Thalidomide-propargyl
|
Others; Ligand for E3 Ligase | Others; PROTAC |
Thalidomide-propargyl 是一种基于 Thalidomide 的 Cereblon 配体,可用于募集 CRBN 蛋白。它能够利用 linker 与靶蛋白配体连接,得到含 IMiD 的 PROTAC。 | |||
T4163 |
Reparixin
DF 1681Y,Repertaxin,瑞帕利辛 |
CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation |
Reparixin (Repertaxin) 是两种 CXCL8 受体 CXCR1/2 的强效抑制剂,它对 CXCR2 介导的细胞迁移具有微弱的抑制作用 ,IC50为 100 nM。它强烈阻断 CXCR1 介导的趋化性,IC50为 1 nM。 | |||
T12367 |
Parsaclisib
INCB050465 |
PI3K | PI3K/Akt/mTOR signaling |
Parsaclisib (INCB050465) 是有效的、选择性的、具有口服活性的PI3Kδ抑制剂,其 IC50=1 nM。它相对于其他 PI3K I 类同工型的选择性约为 20000 倍。它可用于复发或难治性 B 细胞恶性肿瘤的研究。 | |||
T19455 |
N-ε-propargyloxycarbonyl-L-lysine hydrochloride
N6-((Prop-2-yn-1-yloxy)carbonyl)-L-lysine hydrochloride,N-Ε-炔丙氧基羰基-L-赖氨酸盐酸盐,H-L-Lys(Poc)-OH (hydrochloride) |
Others | Others |
N-ε-propargyloxycarbonyl-L-lysine hydrochloride (N6-((Prop-2-yn-1-yloxy)carbonyl)-L-lysine hydrochloride) 是一种基于赖氨酸的非天然氨基酸 (UAA)。它普遍用于多种生物体中荧光探针的生物偶联。 | |||
T12360 |
para-Nitroblebbistatin
p-Nitroblebbistatin |
Myosin | Cytoskeletal Signaling |
para-Nitroblebbistatin (p-Nitroblebbistatin) 是无细胞毒性、无荧光、光稳定、特异性的肌球蛋白 II (Myosin II) 抑制剂。para-Nitroblebbistatin 可用于肌球蛋白 II 在生理学、发育和细胞生物学中特殊作用的相关研究。 | |||
T26296 |
Triparanol
曲帕拉醇,MER-29,NSC 65345,NSC-65345,NSC65345 |
Apoptosis; Hedgehog/Smoothened | Apoptosis; GPCR/G Protein; Stem Cells |
Triparanol (NSC-65345) 干扰 Hedgehog 信号分子的翻译后修饰以及其受体 PTCH1 的甾醇传感域,导致 Hedgehog 信号的下调。 Triparanol 抑制人类肿瘤生长,是一种具有高眼毒性的抗血脂剂。 | |||
T9430 |
Venadaparib
NOV140101,IDX-1197 |
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Venadaparib (NOV140101) 是一种选择性和具有口服活性的 PARP 抑制剂,对 PARP1和 PARP2的 IC50分别为 1.4 和 1.0 nM。它可防止 DNA 单链断裂 (SSB) 的修复,可研究实体瘤。 | |||
T39849 |
Propargite
|
Parasite | Microbiology/Virology |
Propropgite 通过诱导 DNA 损伤来诱导 β 细胞坏死。它诱导 MIN6 细胞死亡的 IC50为 1 μM.。它可用于杀死螨虫。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6194 |
Fidaxomicin
非达米星,Tiacumicin B,OPT-80,Clostomicin B1,PAR-101 |
Apoptosis; DNA/RNA Synthesis; Antibacterial; Antibiotic | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Fidaxomicin (Tiacumicin B) 是一种大环RNA 聚合酶抑制剂,具有窄谱活性。它选择性地根除致病性艰难梭菌,对构成正常健康肠道菌群的多种细菌影响很小。 | |||
T5287 |
N-Acetyl-L-aspartic acid
AC-ASP-OH,N-Acetylaspartic acid,N-乙酰-L-天门冬氨酸 |
Others; Endogenous Metabolite | Metabolism; Others |
N-Acetyl-L-aspartic acid (AC-ASP-OH) 是天冬氨酸的衍生物, 是由氨基酸天冬氨酸和乙酰辅酶 A 在神经元中合成的。 | |||
T5557 |
Propylparaben
羟苯丙酯,Propyl 4-hydroxybenzoate,尼泊金丙酯,Propyl parahydroxybenzoate |
Apoptosis; Endogenous Metabolite; Antibacterial | Apoptosis; Metabolism; Microbiology/Virology |
Propylparaben (Propyl parahydroxybenzoate) 是一种由植物和细菌产生的抗菌防腐剂。它普遍用于化妆品,药品和食品中。它通过改变细胞周期,细胞凋亡和类固醇生成途径来破坏卵泡的生长和类固醇生成功能。它还可降低大鼠的精子数量和活动能力。 | |||
T4973 |
Paraxanthine
1,7-二甲基黄嘌呤,1,7-DIMETHYLXANTHINE |
Endogenous Metabolite | Metabolism |
Paraxanthine (1,7-dimethylxanthine) 是一种 caffeine 的代谢物,能够刺激Ryanodine 受体通道来抑制多巴胺能细胞的死亡。 | |||
T5284 |
N-Carbamoyl-DL-aspartic acid
氨基甲酰-DL-天(门)冬氨酸,N-Carbamoyl-DL-aspartic acid,Ureidosuccinic acid,脲基琥珀酸 |
Others; Endogenous Metabolite | Metabolism; Others |
N-Carbamoyl-DL-aspartic acid (Ureidosuccinic acid) 是核酸嘧啶的前体之一。 | |||
TN3748 |
D-Asparagine
D-天冬酰胺,H-D-Asn-OH |
Others; Endogenous Metabolite | Metabolism; Others |
D-Asparagine (H-D-Asn-OH) 是酵母菌株的氮源。 D-Asparagine 是 L-Asparagine 水解的竞争性抑制剂 (Ki = 0.24 mM)。 | |||
T4885 |
(-)-Aspartic acid
(R)-Aspartic acid,Asp,D-(-)-Aspartic acid,D-天门冬氨酸,Aminosuccinic acid,asparagic acid,L-Homoproline,D-Aspartic acid |
Endogenous Metabolite; NMDAR; iGluR | Membrane transporter/Ion channel; Metabolism; Neuroscience |
(-)-Aspartic acid (L-Homoproline) 是一种存在于无脊椎动物和脊椎动物中的内源性氨基酸,是 NMDA 受体激动剂,可调节睾酮合成。 | |||
TN6762 |
(+)-Cuparene
|
Others | Others |
(+)-Cuparene 是一种生物活性化学品。 | |||
T8392 |
L(+)-Asparagine monohydrate
|
Endogenous Metabolite | Metabolism |
L(+)-Asparagine monohydrate 是一种非必需氨基酸,参与组织细胞功能的神经和代谢调节。 | |||
T4S1820 |
Parishin
巴利森苷A,派立辛,Parishin A |
Others | Others |
Parishin (Parishin A) A 是一种酚类葡萄糖苷,从天麻中分离得到。Parishin 通过调节 Sir2/Uth1/TOR 信号通路而具有抗衰老作用,并延长酵母寿命。 | |||
T65269 |
L-Aspartic acid potasium salt
Aspartic acid potasium salt,Potassium L-aspartate |
Others | Others |
L-aspartic acid potasium salt(VX-548) 是一种广泛存在于动植物体内的氨基酸。L-aspartic acid potasium salt驱动氮氧化物的产生,从而促进吞噬作用,有助于提高鱼类的成活率。L-aspartic acid potasium salt 可对抗生素产生刺激,刺激作用可能与参与天冬氨酸-4-半醛生物合成的前体有关。 | |||
TN3469 |
Aucuparin
2,6-dimethoxy-4-phenylphenol |
NADPH-oxidase | Immunology/Inflammation |
Aucuparin (2,6-dimethoxy-4-phenylphenol) 是一种植物抗菌素,具有抗炎活性。 在博来霉素 (BLM) 诱导的肺纤维化小鼠模型中,Aucuparin 抑制肺纤维化。 在经ABTS 和FRAP 测定显示出明显的清除活性。 Aucuparin 对fmlp 诱导的人中性粒细胞产生超氧化物具有明显的抑制作用,其IC50为17.0μM。 | |||
T19554 |
L-Aspartic aicd sodium
L-Aspartic acid sodium,Sodium L-aspartate |
Others; Sodium Channel; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Others |
L-Aspartic aicd sodium (Sodium L-aspartate) 是一种氨基酸,是一种结肠特异性活性分子输送的前体活性分子,可促进大鼠前脑膜囊泡的 Na+外排。 | |||
T7929 |
L-Aspartic Acid 4-Benzyl Ester
|
Others | Others |
L-Aspartic Acid 4-Benzyl Ester 是一种螯合剂,与金属离子形成稳定的络合物,已用于研究金属离子对酶活性的影响,以及研究金属离子在基因表达调控中的作用等。 | |||
T0792 |
(-)-Sparteine sulfate pentahydrate
(-)-Sparteine Sulfate,Lupinidine sulfate pentahydrate,(-)-Sparteine sulfate salt,sulfate pentahydrate,五水合硫酸司巴丁 |
Sodium Channel | Membrane transporter/Ion channel |
(-)-Sparteine sulfate pentahydrate ((-)-Sparteine Sulfate) 是一种生物碱,是钠通道抑制剂,属于1a 类抗心律失常药。 | |||
T0927 |
Butylparaben
Butyl 4-hydroxybenzoate,Butyl parahydroxybenzoate,尼泊金丁酯,对羟基苯甲酸丁酯 |
Endogenous Metabolite; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology |
Butylparaben (Butyl 4-hydroxybenzoate) 是一种标准化的化学过敏原,可增加组胺释放和细胞介导的免疫。 | |||
T3728 |
Methyl Paraben
尼泊金甲酯,Methyl parahydroxybenzoate,Nipagin,对羟基苯甲酸甲酯,Methylparaben,Methyl 4-hydroxybenzoate,Methyl p-hydroxybenzoate |
Endogenous Metabolite; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology |
Methyl Paraben (Nipagin) 是一种标准化的过敏原,是从云南铁杉中分离出来对羟基苯甲酸的甲酯。它是一种抗菌剂、防腐剂、调味剂。它的生理作用是通过增加组胺释放和细胞调控免疫实现的。 | |||
TN1005 |
Parishin E
巴利森苷E,巴利森苷 E |
Others | Others |
Parishin E 是一种分离自天麻的 Parishin 衍生物,可能具有抗氧化活性。 | |||
T3S1816 |
Parishin B
|
Others | Others |
Parishin B 是一种分离自天麻中的 Parishin 衍生物,可能具有抗氧化活性。 | |||
T2140 |
Parthenolide
(-)-Parthenolide,小白菊内酯 |
Apoptosis; Mitophagy; NF-κB; HDAC; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; NF-κB |
Parthenolide ((-)-Parthenolide) 是一种从药草短舌匹菊中发现的倍半萜内酯。 它抑制NF-κB 活化,有抗炎活性。它还可抑制HDAC1蛋白,但不影响其他I/II 类HDAC。 | |||
T2O2774 |
L-Asparagine
alpha-aminosuccinamic acid,L-天门冬氨酸,(-)-Asparagine,Asparamide,2-Aminosuccinamic acid,Asn,Altheine |
Endogenous Metabolite | Metabolism |
L-Asparagine (Asparamide) 是一种非必需氨基酸,可以参与神经和脑组织细胞功能的代谢控制。 | |||
T4085 |
Paris saponin VII
重楼皂苷 VII,Chonglou Saponin VII,Polyphyllin-VII,Dioscinin,Paris saponin-VII |
Apoptosis; BCL; Others; PARP; p38 MAPK; Akt; Caspase; P-gp; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; MAPK; Membrane transporter/Ion channel; Neuroscience; Others; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Paris saponin VII (Dioscini) 是从延龄草的根和根茎中分离的一种甾体皂苷。它减弱线粒体膜电位,增加凋亡相关蛋白的表达,并降低Bcl-2、caspase-9、caspase-3、PARP-1和p-Akt 的蛋白表达水平。它在 K562/ADR 细胞中诱导强烈的自噬,可研究白血病。 | |||
T0834 |
Ethylparaben
Ethyl 4-hydroxybenzoate,Ethyl parahydroxybenzoate,羟苯乙酯,尼泊金乙酯 |
Antibacterial; Antifungal | Microbiology/Virology |
Ethylparaben (Ethyl parahydroxybenzoate) 是一种标准化的化学过敏原。 对羟基苯甲酸乙酯的生理作用是通过增加组胺释放和细胞介导免疫来实现的。 | |||
T7113 |
Paradol
姜酮酚,6-paradol,必理通,[6]-Gingerone |
COX | Immunology/Inflammation; Neuroscience |
Paradol ([6]-Gingerone) 是一种姜科植物中发现的酚类天然产物,具有抗癌、抗炎、抗氧化和神经保护作用。在小鼠皮肤癌变中,可结合到环氧合酶(COX-2) 活性位点。 | |||
T7853 |
(+)-Sparteine
鹰爪豆碱,(+)-鹰爪豆碱,Pachycarpine |
AChR | Neuroscience |
(+)-Sparteine (Pachycarpine) 是从苏格兰扫帚中提取的一种生物碱,是钠通道阻滞剂和 1a 类抗心律失常剂。它在神经细胞中竞争性地抑制烟碱型乙酰胆碱受体活性,是神经节阻滞剂。 | |||
TN1803 |
Isoscoparin
|
Antioxidant; TNF; NO Synthase; Fatty Acid Synthase | Apoptosis; Immunology/Inflammation; Metabolism; oxidation-reduction |
Isoscoparin 源自 Gentiana algida Pall,具有抗氧化和抗脂肪生成活性。Isoscoparin 可用于预防和治疗肥胖的研究。 | |||
T2O2731 |
L-Aspartic acid
L-天冬氨酸,L-天冬氨酸;L-天冬碱;L-酰胺天冬酸;L-天冬酰胺一水物,Aspatofort,Asparagic acid |
Others; Endogenous Metabolite | Metabolism; Others |
L-Aspartic acid (Aspatofort) 是一种氨基酸,是结肠特异性药物输送的前体药物。 | |||
TMA1603 |
Parishin C
巴利森苷 C,巴利森苷C |
Antioxidant | oxidation-reduction |
Parishin C 是一种从天麻中分离出的 Parishin 衍生物,可能具有抗氧化作用。 | |||
T2729 |
Scoparone
滨蒿内酯,Escoparone,Scoparon,Aesculetin dimethyl ether,6,7-dimethoxycoumarin,6,7-Dimethylesculetin |
Others | Others |
Scoparone (Aesculetin dimethyl ether) 是分离自毛蒿中,具有抗凝血,抗血管舒张作用和抗炎活性。 | |||
T10388 |
Asparagusic acid
1,2-二噻戊环-4-羧酸,芦笋酸 |
Parasite | Microbiology/Virology |
Asparagusic acid 是芦笋植物中的一种含硫气味成分,是植物生长抑制剂,具有抗寄生虫作用。 | |||
T19355 |
Heparan Sulfate
硫酸乙酰肝素,硫酸类肝素 |
FGFR; Wnt/beta-catenin; Endogenous Metabolite | Angiogenesis; Cytoskeletal Signaling; Metabolism; Stem Cells; Tyrosine Kinase/Adaptors |
Heparan sulfate 是一种复杂的线性多糖。Heparan sulfate 作为硫酸乙酰肝素蛋白聚糖的一部分出现,在细胞外基质和细胞表面表达丰富。 | |||
T82956 |
Asparenyldiol
Asparenydiol |
||
Asparenyldiol(Asparenydiol)为一类抗氧化剂且兼具点击化学试剂功能。该化合物含Alkyne基团,能够通过CuAAc与含Azide基团的分子发生反应。 | |||
TN3980 | Epoxyparvinolide | Others | Others |
Epoxyparvinolide是一种天然产物,属于唇形科刺蕊草属,其产品编号为 TN3980,CAS号为 102227-61-2。Epoxyparvinolide可用作对照参考。 | |||
T79971 |
Asparanin A
|
Apoptosis | Apoptosis |
Asparanin A 是一种具有抗癌活性的凋亡 (apoptosis) 诱导剂。它能够通过线粒体和 PI3K/AKT 信号通路使细胞周期在 G0/G1 期停滞,并有效抑制癌细胞生长。此外,Asparanin A 在小鼠Ishikawa子宫内膜癌异种移植模型中显示出显著的体内抑制肿瘤生长效力。 | |||
T37609 |
(rel)-Asperparaline A
|
||
Aspergillimide is a fungal metabolite originally isolated from A. japonicus.1 It reduces nicotinic acetylcholine receptor (nAChR) peak and slowly-desensitizing amplitudes induced by acetylcholine in silkworm (B. mori) larval neurons (IC50s = 20.2 and 39.6 nM, respectively) but has no effect on chicken α3β4-, α4β2-, and α7-containing nAChRs.2 Dietary administration of aspergillimide A (10 μg/g of diet) induces paralysis in silkworm fourth instar larvae.1 Aspergillimide A (10 and 20 mg/kg) reduces... | |||
T31658 |
Epoxyparthenolide
|
||
Epoxyparthenolide is a biochemical. | |||
TN3105 |
5-Dehydroxyparatocarpin K
|
Others | Others |
5-Dehydroxyparatocarpin K是一种天然产物,属于豆科补骨脂属,其产品编号为 TN3105,CAS号为 124858-37-3。5-Dehydroxyparatocarpin K可用作对照参考。 | |||
T35908 |
Paraherquamide E
|
||
Paraherquamide E is a fungal metabolite originally isolated from P. charlesii with anthelmintic and insecticidal activities. It is lethal to C. elegans (LD50 = 6 μg/ml). Paraherquamide E is also lethal to O. fasciatus (LD50 = 0.089 μg/nymph). Oral administration of paraherquamide E (0.5-4 mg/kg) reduces T. colubriformis fecal egg count in gerbils. | |||
T81540 |
Parthenosin
Quercetin 3-O-β-D-glucuronide butyl ester |
||
Parthenosin (Quercetin 3-O-β-D-glucuronide butester) 是从Calligoum foamoides地上部分分离得到的黄酮类化合物,对HepG2和MCF-7细胞系表现出明显的细胞毒性,其IC50值分别为60.46μg/mL和61.4μg/mL。 | |||
TN1802 |
Isoscoparin-2′′O-glucoside
异金雀花素-2”-O-吡喃葡萄糖苷,Isoscoparin-2''-Beta-D-glucopyranoside |
Others | Others |
Isoscoparin-2''-Beta-D-glucopyranoside shows prominent free radical scavenging activity in DPPH assay. | |||
TN4741 |
Parvifuran
檀木 |
Others | Others |
Parvifuran is a natural product from Dalbergia parviflora. | |||
T40442 |
Propylparaben sodium
Propyl4-hydroxybenzoatesodium,羟苯丙酯钠,Propylparahydroxybenzoatesodium |
||
Propylparaben sodium (propyl parahydroxybenzoate) is a naturally occurring antimicrobial preservative found in plants and bacteria. Widely utilized in cosmetics, pharmaceuticals, and foods, this compound impairs antral follicle growth and steroidogenic function by modifying the cell-cycle, apoptosis, and steroidogenesis pathways. Additionally, propylparaben sodium reduces sperm count and motility in rats. | |||
TMA2106 | (-)-Sparteine | P450 | Metabolism |
Sparteine is a class 1a antiarrhythmic agent, a sodium channel blocker. The deficient debrisoquine hydroxylation of Sparteine is due to the absence of P-450IID1 protein in the livers of poor metabolizers. | |||
TN3046 |
4-Hydroxysapriparaquinone
|
||
4-Hydroxysapriparaquinone 从Salvia prionitis Hance.的根中分离出的化合物,具有潜在的抗癌活性。 | |||
T79984 |
Chaparrinone
|
Parasite | Microbiology/Virology |
Chaparrinone为苦木素类化合物,源自Eurycoma Harmandiana根部提取。该物质对Plasmodium falciparum和P-388细胞展示出抗疟及细胞毒效应,IC50值分别为0.037 μg/mL和0.34 μg/mL。 | |||
T31531 |
Disparlure
AI334886,AI3-34886,AI3 34886 |
||
Disparlure is a Pheromone. | |||
TN2596 |
12-Hydroxy-2,3-dihydroeuparin
|
Others | Others |
12-Hydroxy-2,3-dihydroeuparin是一种天然产物,属于菊科泽兰属,其产品编号为 TN2596,CAS号为 68776-42-1。12-Hydroxy-2,3-dihydroeuparin可用作对照参考。 | |||
TN2693 |
2,3-Dihydro-12,13-dihydroxyeuparin
|
Others | Others |
2,3-Dihydro-12,13-dihydroxyeuparin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2693,CAS号为 135531-75-8。 | |||
TN5041 | Spartioidine | Others | Others |
Spartioidine是一种天然产物,属于菊科千里光属,其产品编号为 TN5041,CAS号为 520-59-2。Spartioidine可用作对照参考。 | |||
TN6454 | Parvisoflavanone | ||
Parvisoflavanone may have α-Glucosidase inhibitory activity. | |||
------------------------ 更多 ------------------------ |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-01257 |
uPAR/PLAUR Protein, Mouse, Recombinant (His)
uPAR,Cd87,u-PAR,plasminogen activator, uro... |
Mouse | HEK293 |
Urokinase plasminogen activator (uPA) and/or its receptor (uPAR) are essential for metastasis, and overexpression of these molecules is strongly correlated with poor prognosis in a variety of malignant tumours. uPAR and uPA levels in both resected tumor tissue and plasma are of independent prognostic significance for patient survival in several types of human cancer. This system has classically been thought to drive tumor progression by mediating directed extracellular proteolysis on the surface... | |||
TMPY-02141 |
uPAR/PLAUR Protein, Human, Recombinant (His)
UPAR,CD87,plasminogen activator, urokinase receptor... |
Human | HEK293 |
Urokinase plasminogen activator (uPA) and/or its receptor (uPAR) are essential for metastasis, and overexpression of these molecules is strongly correlated with poor prognosis in a variety of malignant tumours. uPAR and uPA levels in both resected tumor tissue and plasma are of independent prognostic significance for patient survival in several types of human cancer. This system has classically been thought to drive tumor progression by mediating directed extracellular proteolysis on the surface... | |||
TMPK-00228 |
uPAR/PLAUR Protein, Human, Recombinant (hFc)
U-PAR,PLAUR,uPAR,MO3,CD87 |
Human | HEK293 |
The receptor (u-PAR) for urokinase plasminogen activator (u-PA) is a three-domain protein, GPI-anchored to the cell surface, which focuses the enzymatic activity of u-PA, and allows the cell surface activation of plasminogen.Regulation of the activity of u-PA is also mediated by u-PAR. | |||
TMPK-00226 |
uPAR/PLAUR Protein, Human, Recombinant (His & Avi)
CD87,uPAR,U-PAR,MO3,PLAUR |
Human | HEK293 |
The receptor (u-PAR) for urokinase plasminogen activator (u-PA) is a three-domain protein, GPI-anchored to the cell surface, which focuses the enzymatic activity of u-PA, and allows the cell surface activation of plasminogen.Regulation of the activity of u-PA is also mediated by u-PAR. | |||
TMPK-00227 |
uPAR/PLAUR Protein, Human, Recombinant (His & Avi), Biotinylated
CD87,PLAUR,U-PAR,MO3,uPAR |
Human | HEK293 |
The receptor (u-PAR) for urokinase plasminogen activator (u-PA) is a three-domain protein, GPI-anchored to the cell surface, which focuses the enzymatic activity of u-PA, and allows the cell surface activation of plasminogen.Regulation of the activity of u-PA is also mediated by u-PAR. | |||
TMPK-00215 |
uPAR/PLAUR isoform 1 Protein, Mouse, Recombinant (His & Avi)
CD87,UPAR,PLAUR,MO3,U-PAR |
Mouse | HEK293 |
The receptor (u-PAR) for urokinase plasminogen activator (u-PA) is a three-domain protein, GPI-anchored to the cell surface, which focuses the enzymatic activity of u-PA, and allows the cell surface activation of plasminogen.Regulation of the activity of u-PA is also mediated by u-PAR. | |||
TMPK-00216 |
uPAR/PLAUR Protein, Mouse, Recombinant (His & Avi), Biotinylated
U-PAR,PLAUR,MO3,CD87,uPAR |
Mouse | HEK293 |
The receptor (u-PAR) for urokinase plasminogen activator (u-PA) is a three-domain protein, GPI-anchored to the cell surface, which focuses the enzymatic activity of u-PA, and allows the cell surface activation of plasminogen.Regulation of the activity of u-PA is also mediated by u-PAR. | |||
TMPK-01175 |
uPAR/PLAUR Protein, Cynomolgus, Recombinant (His)
U-PAR,UPAR,MO3,CD87,PLAUR |
Cynomolgus | HEK293 |
The receptor (u-PAR) for urokinase plasminogen activator (u-PA) is a three-domain protein, GPI-anchored to the cell surface, which focuses the enzymatic activity of u-PA, and allows the cell surface activation of plasminogen.Regulation of the activity of u-PA is also mediated by u-PAR. | |||
TMPY-01017 |
uPAR/PLAUR Protein, Mouse, Recombinant (His & hFc)
plasminogen activator, urokinase receptor,u-PAR,u |
Mouse | HEK293 |
Urokinase plasminogen activator (uPA) and/or its receptor (uPAR) are essential for metastasis, and overexpression of these molecules is strongly correlated with poor prognosis in a variety of malignant tumours. uPAR and uPA levels in both resected tumor tissue and plasma are of independent prognostic significance for patient survival in several types of human cancer. This system has classically been thought to drive tumor progression by mediating directed extracellular proteolysis on the surface... | |||
TMPY-03596 |
JTB Protein, Human, Recombinant (mFc)
PAR,hJT,jumping translocation breakpoint,JTB,HSPC22... |
Human | HEK293 |
Jumping translocation breakpoint, also known as JTB, is a member of the JTB family. Jumping translocation (JT) is an unbalanced translocation that comprises amplified chromosomal segments jumping to various telomeres. JTB is expressed in all normal human tissues studied but overexpressed or underexpressed in many of their malignant counterparts. It is required for normal cytokinesis during mitosis. JTB plays a role in the regulation of cell proliferation. It may be a component of the chromosomal... | |||
TMPY-05025 |
Thrombin Receptor Protein, Human, Recombinant (His)
TR,PAR1,HTR,coagulation factor II (thrombin) recept... |
Human | HEK293 |
Thrombin Receptor Protein, Human, Recombinant (His) is expressed in HEK293 with His tag. The predicted molecular weight is 10.2 kDa. Accession number: A0A024RAP7 | |||
TMPY-06150 |
Par j 2 Protein, Parietaria judaica, Recombinant (His)
|
Parietaria judaica | HEK293 |
Par j 2 is one of the major allergens of the Parietaria judaica. Plant non-specific lipid-transfer proteins transfer phospholipids as well as galactolipids across membranes. May play a role in wax or cutin deposition in the cell walls of expanding epidermal cells and certain secretory tissues. The major allergens from P. judaica pollen, Par j 1 and Par j 2, have amino acid sequence identity of 45% and contain eight cysteine residues involved in disulphide bonds that compact the structure. | |||
TMPY-04180 |
PfLDH Protein, P. falciparum, Recombinant (His)
PfLDH,L-lactate dehydrogenase |
P. falciparum | E. coli |
Plasmodium falciparum lactate dehydrogenase (PfLDH) is a key enzyme for energy generation of malarial parasites and is considered to be a potential antimalarial target. The ability of PfLDH- or PfIDEh-based immuno-PCR assays to detect <1 parasite/microL suggests that improvements of bound antibody sensor technology may greatly increase the sensitivity of malaria rapid diagnostic tests. The PfLDH test could be used to detect failures and, therefore, to assess anti-malarial efficacy. | |||
TMPY-01188 |
PARP Protein, Human, Recombinant (His)
ADPRT1,ADPRT,pADPRT-1,PPOL,ARTD1,PARP-1,poly (ADP-r... |
Human | Baculovirus-Insect Cells |
Poly (ADP-ribose) polymerase 1(PRAP1), also known as NAD(+) ADP-ribosyltransferase 1(ADPRT), is a chromatin-associated enzyme that modifies various nuclear proteins by poly(ADP-ribosyl)ation. The ADP-D-ribosyl group of NAD+ is transferred to an acceptor carboxyl group on a histone or the enzyme itself, and further ADP-ribosyl groups are transferred to the 2'-position of the terminal adenosine moiety, building up a polymer with an average chain length of 2-3 units. The poly(ADP-ribosyl)ation modi... | |||
TMPY-02575 |
PPAR gamma/PPARG Protein, Human, Recombinant (His & GST)
CIMT1,PPARγ,GLM1,PPARgamma,PPARG1... |
Human | Baculovirus-Insect Cells |
Peroxisome proliferator-activated receptor gamma (PPARG), a nuclear hormone receptor, plays a critical role in the lipid and glucose homeostasis, adipocyte differentiation, as well as intracellular insulin-signaling events. The peroxisome proliferator-activated receptor gamma (PPARgamma) regulates osteoblast and osteoclast differentiation, and is the molecular target of thiazolidinediones (TZDs), insulin sensitizers that enhance glucose utilization and adipocyte differentiation. Peroxisome proli... | |||
TMPH-03765 |
Virus-Like Particles (VLPs) isotype control
|
HEK293 | |
Virus-Like Particles (VLPs) isotype control can be used as the control of VLP expressed proteins. | |||
TMPY-00483 |
Parvalbumin/PVALB Protein, Human, Recombinant (His)
parvalbumin,D22S749 |
Human | E. coli |
Parvalbumins (PVALBs) are particularly abundant in the fast-contracting muscles and correlate positively with muscle relaxation speed in amphibians and fishes. The loss of PVALB plays a role in the pathogenesis of thyroid tumors. The mutations in the PVALB gene are not involved in GS patients who harbour a single or no mutant SLC12A3 allele. | |||
TMPY-02043 |
PARK7/DJ-1 Protein, Human, Recombinant (His)
DJ1,HEL-S-67p,DJ-1,parkinson protein 7 |
Human | E. coli |
Parkinson's disease locus DJ-1 (PARK7) is a differentially expressed transcript. DJ-1 plays a physiologic role in protection of erythroid cells from oxidant damage, a function unmasked in the context of oxidative stress. PARK7 belongs to the peptidase C56 family of proteins. It acts as a positive regulator of androgen receptor-dependent transcription. It may also function as a redox-sensitive chaperone, as a sensor for oxidative stress, and it apparently protects neurons against oxidative stress... | |||
TMPH-01840 |
Human parainfluenza 1 virus (HPIV-1) Hemagglutinin-neuraminidase Protein (His)
|
HPIV-1 | E. coli |
Attaches the virus to sialic acid-containing cell receptors and thereby initiating infection. Binding of HN protein to the receptor induces a conformational change that allows the F protein to trigger virion/cell membranes fusion.; Neuraminidase activity ensures the efficient spread of the virus by dissociating the mature virions from the neuraminic acid containing glycoproteins. | |||
TMPH-01849 |
Human parvovirus B19 (isolate AU) Non-capsid protein NS-1 (His & SUMO)
|
HPV B19 | E. coli |
Multifunctional protein essential for viral DNA replication, which cooperatively interacts with the viral DNA origin of replication and transactivates several promoters including the viral p6 promoter. Binds the origin of replication and performs an endonucleolytic nick within a conserved sequence in the viral genome, thereby initiating the rolling circle replication (RCR). Participates in the transcriptional regulation the viral p6 promoter that regulates all viral transcripts and the cellular ... | |||
TMPH-02993 |
DisA Protein, Mycobacterium paratuberculosis, Recombinant (His & Myc)
disA,c-di-AMP synthase,DNA integrity scanning protein DisA,D... |
Mycobacterium paratuberculosis | E. coli |
Participates in a DNA-damage check-point. DisA forms globular foci that rapidly scan along the chromosomes searching for lesions.; Has also diadenylate cyclase activity, catalyzing the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP). c-di-AMP likely acts as a signaling molecule that may couple DNA integrity with a cellular process. | |||
TMPH-00762 |
Parvalbumin beta Protein, Gadus morhua, Recombinant (His & SUMO)
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Gadus morhua | E. coli |
In muscle, parvalbumin is thought to be involved in relaxation after contraction. It binds two calcium ions. | |||
TMPH-03142 |
Plasmepsin-2 Protein, Plasmodium falciparum, Recombinant (E. coli, His & Myc)
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Plasmodium falciparum | E. coli |
During the asexual blood stage, participates in initial cleavage of native host hemoglobin (Hb) resulting in Hb denaturation. May cleave preferentially denatured hemoglobin that has been cleaved by PMI. Digestion of host Hb is an essential step which provides the parasite with amino acids for protein synthesis, and regulates osmolarity (Probable). | |||
TMPH-03140 |
Plasmepsin-1 Protein, Plasmodium falciparum, Recombinant (His)
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Plasmodium falciparum | E. coli |
During the asexual blood stage, catalyzes the initial cleavage of native host hemoglobin (Hb) resulting in Hb denaturation; specifically cleaves between Phe-33 and Leu-34 of Hb alpha-chain. Digestion of host Hb is an essential step which provides the parasite with amino acids for protein synthesis, and regulates osmolarity (Probable). | |||
TMPY-05689 |
Human parainfluenza virus 4b (HPIV-4b) Hemagglutinin-neuraminidase Protein (aa 48-579, His)
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HPIV-4 | Baculovirus-Insect Cells |
Human parainfluenza virus 4b (HPIV-4b) Hemagglutinin-neuraminidase Protein (aa 48-579, His) is expressed in Baculovirus-Insect Cells with His tag. The predicted molecular weight is 57.12 kDa. Accession number: A0A1V0E1S6 | |||
TMPY-04181 |
pfHPRT Protein, P. falciparum, Recombinant (His)
pfHPRT |
P. falciparum | E. coli |
pfHPRT Protein, P. falciparum, Recombinant (His) is expressed in E. coli with His tag. The predicted molecular weight is 28.6 kDa. Accession number: Q76NM3 | |||
TMPY-06830 |
PPAR alpha/PPARA Protein, Human, Recombinant (His)
NR1C1,PPARα,peroxisome proliferator-activated recep... |
Human | E. coli |
Peroxisome proliferators include hypolipidemic drugs, herbicides, leukotriene antagonists, and plasticizers; this term arises because they induce an increase in the size and number of peroxisomes. Peroxisomes are subcellular organelles found in plants and animals that contain enzymes for respiration and for cholesterol and lipid metabolism. The action of peroxisome proliferators is thought to be mediated via specific receptors, called PPARs, which belong to the steroid hormone receptor superfami... | |||
TMPY-00090 |
SPARCL1 Protein, Mouse, Recombinant (His)
Sc1,SPARC like 1,mast9,hevin,Ecm2 |
Mouse | HEK293 |
SPARC-like protein 1 (SPARCL1; also known as SC1, high endothelial venule protein, or hevin) is an extracellular matrix-associated, secreted glycoprotein belonging to the secreted protein acidic and rich in cysteine (SPARC) family of matricellular proteins. It contains three conserved structural domains that are implicated in the regulation of cell adhesion, migration, and proliferation. SPARCL1 is expressed during embryogenesis and tissue remodeling and is especially prominent in brain and vasc... | |||
TMPY-04814 |
SPARC Protein, Rat, Recombinant (His)
SPARC,secreted protein, acidic, cysteine-rich (oste... |
Rat | HEK293 |
Secreted protein acidic and rich in cysteine (SPARC), also known as Osteonectin (ON), is a member of the SPARC family. SPARC consists of three domains: an EF-hand domain, a follistatin-like domain and a Kazal-like domain, and each of which has independent activity and unique properties. The activity of SPARC is context- and cell-type-dependent, which is highlighted by the fact that SPARC has shown seemingly contradictory effects on tumor progression in both clinical correlative studies and in an... | |||
TMPY-02465 |
PARP Protein, Mouse, Recombinant (His)
AI893648,Adprp,5830444G22Rik,C80510,sPARP-1,poly (A... |
Mouse | Baculovirus-Insect Cells |
Poly (ADP-ribose) polymerase 1(PRAP1), also known as NAD(+) ADP-ribosyltransferase 1(ADPRT), is a chromatin-associated enzyme that modifies various nuclear proteins by poly(ADP-ribosyl)ation. The ADP-D-ribosyl group of NAD+ is transferred to an acceptor carboxyl group on a histone or the enzyme itself, and further ADP-ribosyl groups are transferred to the 2'-position of the terminal adenosine moiety, building up a polymer with an average chain length of 2-3 units. The poly(ADP-ribosyl)ation modi... | |||
TMPH-01844 |
Paralemmin-1/PALM Protein, Human, Recombinant (His)
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Human | E. coli |
Involved in plasma membrane dynamics and cell process formation. Isoform 1 and isoform 2 are necessary for axonal and dendritic filopodia induction, for dendritic spine maturation and synapse formation in a palmitoylation-dependent manner. | |||
TMPH-01841 |
Human parainfluenza 1 virus (HPIV-1) Nucleoprotein/NP Protein (His)
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HPIV-1 | E. coli |
Encapsidates the genome in a ratio of 1 N per 6 ribonucleotides, protecting it from nucleases. The nucleocapsid (NC) has a helical structure. The encapsidated genomic RNA is termed the NC and serves as template for transcription and replication. During replication, encapsidation by N is coupled to RNA synthesis and all replicative products are resistant to nucleases. | |||
TMPH-01942 |
PARP14 Protein, Human, Recombinant (His & Myc)
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Human | HEK293 |
PARP14 Protein, Human, Recombinant (His & Myc) is expressed in HEK293. | |||
TMPH-03137 |
PFS230 Protein, Plasmodium falciparum, Recombinant
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Plasmodium falciparum | E. coli |
Gametocyte surface protein required for male/female gamete fusion. Also required for male gamete exflagellation and interaction with erythrocytes. | |||
TMPH-03141 |
Plasmepsin-2 Protein, Plasmodium falciparum, Recombinant (His & Myc)
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Plasmodium falciparum | Baculovirus |
During the asexual blood stage, participates in initial cleavage of native host hemoglobin (Hb) resulting in Hb denaturation. May cleave preferentially denatured hemoglobin that has been cleaved by PMI. Digestion of host Hb is an essential step which provides the parasite with amino acids for protein synthesis, and regulates osmolarity (Probable). | |||
TMPH-01944 |
PARP9 Protein, Human, Recombinant (His & Myc)
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Human | HEK293 |
PARP9 Protein, Human, Recombinant (His & Myc) is expressed in HEK293. | |||
TMPH-03138 |
GST Protein, Plasmodium falciparum, Recombinant (His)
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Plasmodium falciparum | Yeast |
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. May also function as a storage protein or ligandin for parasitotoxic ferriprotoporphyrin IX (hemin). | |||
TMPH-01881 |
PARP2 Protein, Human, Recombinant (GST & His)
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Human | Baculovirus |
PARP2 Protein, Human, Recombinant (GST & His) is expressed in Baculovirus with N-terminal GST tag and C-terminal 6xHis tag. The predicted molecular weight is 92.8 kDa. Accession number: Q9UGN5 | |||
TMPH-02995 |
MAP_1030 Protein, Mycobacterium paratuberculosis, Recombinant (His)
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Mycobacterium paratuberculosis | Yeast |
MAP_1030 Protein, Mycobacterium paratuberculosis, Recombinant (His) is expressed in Yeast with N-terminal 6xHis tag. The predicted molecular weight is 28.8 kDa. Accession number: P62039 | |||
TMPY-06351 |
Virus-Like Particle (VLP) isotype control Protein
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HEK293 | |
Virus-Like Particle (VLP) isotype control Protein is expressed in HEK293. The predicted molecular weight is . | |||
TMPJ-00242 |
PARVA Protein, Human, Recombinant (His)
PARVA,CH-ILKBP,Actopaxin,Alpha-Parvin,Matr... |
Human | E. coli |
Alpha-Parvin (PARVA) is a member of the Parvin family. PARVA contains two CH (calponin-homology) domains. PARVA is widely expressed, with highest levels in heart, skeletal muscle, kidney and liver. PARVA interacts with integrin-linked protein kinase and probably with actin and the LD1 and LD4 motifs of PXN. PARVA may play a role in the regulation of cell adhesion and cytoskeleton organization. PARVA is also involved in ciliogenesis. | |||
TMPY-01109 |
Influenza A H1N1 (A/California/04/2009) Hemagglutinin/HA Protein ((IQS→RQRRRRK, HA1+HA2, partially cleaved,His)
Harvey rat sarcoma viral oncogene homolog |
H1N1 | HEK293 |
The influenza viral Hemagglutinin (HA) protein is a homotrimer with a receptor binding pocket on the globular head of each monomer.HA has at least 18 different antigens. These subtypes are named H1 through H18.HA has two functions. Firstly, it allows the recognition of target vertebrate cells, accomplished through the binding to these cells' sialic acid-containing receptors. Secondly, once bound it facilitates the entry of the viral genome into the target cells by causing the fusion of the host ... | |||
TMPK-00657 |
SPARC Protein, Cynomolgus, Recombinant (His)
BM-40,EGM_15571,SPARC,ON |
Cynomolgus | HEK293 |
Secreted protein acidic and rich in cysteine (SPARC/osteonectin/BM40) is one of the most abundant non-collagenous protein expressed in mineralized tissues.The capacity of SPARC to influence pathways involved in extracellular matrix assembly such as procollagen processing and collagen fibril formation as well as the capacity to influence osteoblast differentiation and osteoclast activity will be addressed. | |||
TMPH-00817 |
Pectate lyase 1 Protein, Hesperocyparis arizonica, Recombinant (His & Myc)
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Hesperocyparis arizonica | E. coli |
Has pectate lyase activity. | |||
TMPH-02827 |
PPAR gamma Protein, Mouse, Recombinant (His)
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Mouse | E. coli |
Nuclear receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the nuclear receptor binds to DNA specific PPAR response elements (PPRE) and modulates the transcription of its target genes, such as acyl-CoA oxidase. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. ARF6 acts as a key regulator of the tissue-specific adipocyte P2 (aP2) enhanc... | |||
TMPH-01883 |
PARN Protein, Human, Recombinant (His)
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Human | E. coli |
3'-exoribonuclease that has a preference for poly(A) tails of mRNAs, thereby efficiently degrading poly(A) tails. Exonucleolytic degradation of the poly(A) tail is often the first step in the decay of eukaryotic mRNAs and is also used to silence certain maternal mRNAs translationally during oocyte maturation and early embryonic development. Interacts with both the 3'-end poly(A) tail and the 5'-end cap structure during degradation, the interaction with the cap structure being required for an eff... | |||
TMPH-01879 |
PARP11 Protein, Human, Recombinant (His)
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Human | E. coli |
Mono-ADP-ribosyltransferase that mediates mono-ADP-ribosylation of target proteins. Plays a role in nuclear envelope stability and nuclear remodeling during spermiogenesis. | |||
TMPH-00763 |
Parvalbumin beta Protein, Gadus morhua subsp. callarias, Recombinant (His)
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Gadus callarias | E. coli |
In muscle, parvalbumin is thought to be involved in relaxation after contraction. It binds two calcium ions. | |||
TMPH-03711 |
PPAR gamma Protein, Xenopus laevis, Recombinant (His)
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Xenopus laevis | E. coli |
Receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the receptor binds to a promoter element in the gene for acyl-CoA oxidase and activates its transcription. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. | |||
TMPH-00961 |
Aspartoacylase Protein, Human, Recombinant (His & Myc)
Aminoacylase-2,ACY2,ACY-2,ASP,ASPA,Aspartoacylase |
Human | HEK293 |
Aspartoacylase Protein, Human, Recombinant (His & Myc) is expressed in HEK293. | |||
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