203
30
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6532 |
Hesperadin
|
Influenza Virus; Parasite; Aurora Kinase; Autophagy | Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Microbiology/Virology |
Hesperadin 是 Aurora A 和 B 的 ATP 竞争性吲哚酮抑制剂,抑制 Aurora B 的 IC50值为250nM。它通过阻断核分裂和胞质分裂而抑制布鲁氏锥虫的生长。它也是一种广谱流感抗病毒剂。 | |||
T14511 |
BAY1082439
N-[8-[[(2R)-2-羟基-3-(吗啉-4-基)丙基]氧基]-7-甲氧基-2,3-二氢咪唑并[1,2-C]喹唑啉-5-基]-2-甲基吡啶-3-甲酰胺 |
Apoptosis; PI3K | Apoptosis; PI3K/Akt/mTOR signaling |
BAY1082439 是一种具有口服活性的,选择性 PI3Kα/β/δ抑制剂。它也能抑制 PIK3CA 的突变形式,它对抑制 Pten 丢失的前列腺癌的生长有很强的作用。 | |||
T9304 |
(S)-Sunvozertinib
N-[5-[[4-[5-Chloro-4-fluoro-2-(2-hydroxypropan-2-yl)anilino]pyrimidin-2-yl]amino]-2-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-4-methoxyphenyl]prop-2-enamide,DZD9008 |
EGFR; HER | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
(S)-Sunvozertinib (DZD9008) 是 Sunvozertinib 的 S-对映体,能够抑制EGFR 外显子 20 NPH 和 ASV 插入、EGFR L858R/T790M 突变及 Her2 外显子 20 YVMA 插入,也能够抑制BTK。 | |||
T14766 |
BPH-715
|
Others; Parasite | Microbiology/Virology; Others |
BPH-715 抑制恶性疟原虫的肝脏阶段生长,对 HepG2 细胞中的恶性疟原虫外红细胞的形成的 IC50 为 10 μM。 | |||
T8652 |
CASP3 Activator 1541
|
Caspase | Apoptosis; Proteases/Proteasome |
CASP3 Activator 1541 是 caspase-3 酶原形式的激活剂,可诱导细胞死亡。 | |||
T3579 |
PLX8394
|
Raf | MAPK |
PLX8394 是一种口服活性的丝氨酸/苏氨酸蛋白激酶 B-Raf (BRAF) 蛋白抑制剂。 PLX8394 可以选择性地结合并抑制野生型和突变形式的 BRAF 的活性,然后抑制表达 BRAF 突变形式的肿瘤细胞的增殖。 PLX8394 似乎对表达多种激酶突变形式的肿瘤有效,并且可能是对其他对 BRAF V600E 突变体特异的 BRAF 抑制剂疗法耐药的肿瘤的有效治疗剂。 | |||
T0707L |
Cyclophosphamide
|
DNA Alkylator/Crosslinker; DNA; MRP | DNA Damage/DNA Repair; Immunology/Inflammation |
Cyclophosphamide 是一种烷化剂,具有抗肿瘤及免疫抑制活性,用于治疗多种癌症。 | |||
T20736 |
Cryptating agent 222
Cryptate 222,NSC 264495,NSC-264495,NSC264495 |
Others | Others |
Cryptating agent 222 (NSC-264495) 是穴状配体,与钾镜一起使用以将受阻二锡烯还原为结晶自由基阴离子并与金属阳离子形成配体。 | |||
T13584 |
BMVC-8C3O
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
BMVC-8C3O 是一种 DNA G-四链体 (G4) 配体,可诱导人类端粒 DNA G4 中的非平行到平行形式的拓扑转换 | |||
T3024 |
Avitinib
AC0010,艾维替尼 |
EGFR; JAK; BTK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors |
Avitinib (AC0010) 是一种不可逆的、突变体选择性的EGFR 抑制剂,可有效抑制非小细胞肺癌中EGFR T790M 耐药突变。阿比替尼也是一种新型BTK 抑制剂。 | |||
T5885 |
N-Acetyl-D-galactosamine
GalNAc,2-乙酰胺基-2-脱氧-D-半乳糖 |
Others | Others |
N-Acetyl-D-galactosamine (GalNAc) 是一种源自半乳糖的末端必需氨基糖,在人体中形成 A 型血的抗原。 | |||
T6918 |
Olmutinib
HM61713, BI 1482694,奥莫替尼,BI 1482694,HM61713 |
EGFR; BTK | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Olmutinib (HM61713, BI 1482694) 是可口服的不可逆 EGFR 酪氨酸激酶抑制剂,其与激酶结构域附近的半胱氨酸残基结合,可用于非小细胞肺癌的研究。 | |||
T18595 |
Dasatinib carbaldehyde
PROTAC ABL binding moiety 4,BMS-354825 carbaldehyde |
Others; Ligands for Target Protein for PROTAC | Others; PROTAC |
Dasatinib carbaldehyde (PROTAC ABL binding moiety 4) 基于 ABL 抑制剂达沙替尼,通过接头与 IAP 配体结合,形成 SNIPER [1]。 | |||
T2346 |
Enasidenib
恩西地平,AG-221 |
Dehydrogenase; Isocitrate Dehydrogenase (IDH) | Metabolism |
Enasidenib (AG-221) 是口服具有活力的、可逆的、选择性IDH2突变酶抑制剂,抑制IDH2R140Q 和 IDH2R172K 的IC50分别为100 和 400 nM。 | |||
T9473 |
4SC-203
|
FLT | Angiogenesis; Tyrosine Kinase/Adaptors |
4SC-203 是一种具有潜在的抗肿瘤活性的多激酶抑制剂。它对 FLT3/STK1、 FLT3 的突变形式以及 VEGFRs 具有选择性抑制作用。 | |||
T10989 |
Dehydroaripiprazole
OPC-14857,DM-14857 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Dehydroaripiprazole (DM-14857) 是 Aripiprazole 的活性代谢产物,具有抗精神病活性。Aripiprazole 是也一种抗精神病药。 | |||
T20346 |
Salicylaldoxime
|
Others | Others |
Salicylaldoxime 是一种螯合剂,有时用于分析含有过渡金属离子的样品,它通常与过渡金属离子形成色彩鲜艳的配位络合物。 | |||
T0951 |
Hydroxychloroquine sulfate
Acidum iopanoicum,硫酸羟基氯喹,硫酸羟氯喹,HCQ sulfate |
DNA; SARS-CoV; TLR; Parasite; Autophagy | Autophagy; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology |
Hydroxychloroquine sulfate (Acidum iopanoicum) 抑制疟原虫血红素聚合酶。它还可抑制 Toll 样受体 7/9 信号传导和 SARS-CoV-2 感染。 | |||
T14054 |
5-TAMRA-SE
5-羧基四甲基罗丹明琥珀酰亚胺酯,5-Carboxytetramethylrhodamine succinimidyl ester,5-TAMRA-NHS ester |
Others | Others |
5-TAMRA-SE 是一种胺反应性荧光剂。它的结合物能够产生一种 pH 不敏感的、明亮的橙红色荧光(Ex/Em~546/579 nm),具有良好的光稳定性。 | |||
T2662 |
Alda-1
Alda 1 |
Apoptosis; Dehydrogenase | Apoptosis; Metabolism |
Alda-1是一种 ALDH2 激动剂,是野生型 ALDH2*1 和亚洲 E487K 突变体 ALDH2*2 形式的线粒体醛脱氢酶 2 的细胞渗透激活剂。 | |||
T4325 |
COTI-2
COTI 2,COTI2 |
Apoptosis; p53 | Apoptosis |
COTI-2是一种具有口服活性的低毒性抗癌药物,是 p53 突变体激活剂。它通过激活突变型 p53 和抑制PI3K/AKT/mTOR 途径发挥作用,通过 p53 依赖和非依赖机制在 HNSCC 中具有抗肿瘤活性。它诱导多种人肿瘤细胞凋亡,可将突变型 p53 转化为野生型构象。 | |||
T5420 |
Cycloguanil hydrochloride
Chloroguanide Triazine,环氯胍盐酸盐 |
Parasite; Drug Metabolite | Metabolism; Microbiology/Virology |
Cycloguanil hydrochloride (Chloroguanide Triazine) 是抗疟化合物氯胍的活性代谢物。 它作为二氢叶酸还原酶的抑制剂,对于疟原虫和人类形式的 Kis 值分别为 0.3 和 1.5 nM。 | |||
T17697 |
BRD7-IN-1
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
BRD7-IN-1 是一种修饰的 BI7273 衍生物 (BRD7/9 抑制剂)。BRD7-IN-1 通过与 VHL 配体连接形成 PROTAC VZ185。VZ185 抑制 BRD7/9 的 DC50分别是 4.5 nM 和1.8 nM。 | |||
T0033 |
Miltefosine
HePC,米替福新,Hexadecyl phosphocholine |
Akt; HIV Protease; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Miltefosine (HePC) 是一种广谱抗微生物剂,是治疗内脏和皮肤利什曼病的药物。它是 CTP 磷酸胆碱胞苷基转移酶的抑制剂。 | |||
T2410 |
Nedaplatin
奈达铂,NSC 375101D |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Nedaplatin (NSC-375101D) 是顺铂的衍生物,是肿瘤集落形成单位的 DNA 损伤剂,IC50为94 μM。 | |||
T1055 |
Ifosfamide
NSC109724,Isophosphamide,异环磷酰胺 |
DNA Alkylator/Crosslinker; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Ifosfamide (NSC-109724) 是一种烷化剂,具有抗肿瘤活性。它烷基化并形成 DNA 交联,从而防止 DNA 链分离和 DNA 复制。它是一种前药,必须通过肝微粒体酶的羟基化来激活。 | |||
T21434 |
Sulfacetamide
NSC 63871,磺胺醋酰,NSC-63871,Sebizon,Region,NSC63871,Sulphacetamide,Acetosulfamine |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Sulfacetamide (NSC-63871) 是一种抗生素,通过限制细菌生存所需的叶酸的存在来治疗睑缘炎或结膜炎,有潜力用于眼部感染的研究。 | |||
T76681 |
Fresolimumab
GC1008 |
TGF-beta/Smad | Stem Cells |
Fresolimumab (GC1008) 是一种具有特异性的人抗转化生长因子 β单克隆抗体,可与人 TGFβ1、TGFβ2 和 TGFβ3 的活性形式结合,可用于研究成人局灶节段性肾小球硬化和癌症。 | |||
T2307 |
Icotinib Hydrochloride
埃克替尼盐酸盐,盐酸埃克替尼,BPI-2009H |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Icotinib Hydrochloride (BPI-2009H) 是一种口服的基于喹唑啉的表皮生长因子受体 (EGFR) 抑制剂,IC50值为5 nM,具有潜在的抗肿瘤活性。 | |||
T5095 |
Oxazolone
4-乙氧基亚甲基-2-苯基-2-唑啉-5-酮,4-Ethoxymethylene-2-phenyl-2-oxazolin-5-one |
Others | Others |
Oxazolone 已被用作半抗原化剂,可在成年斑马鱼肠道组织中诱导炎症反应,并可用作两种形式的炎症性肠病(如克罗恩病和溃疡性结肠炎)的基因表达研究模型。 | |||
T17182 |
TX1-85-1
|
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
TX1-85-1 是不可逆 Her3 抑制剂,IC50值为 23 nM。它诱导 Her3 蛋白部分降解,并减弱 Her3 依赖性信号传导。它是选择性 Her3 配体,与位于 Her3 的 ATP 结合位点的 Cys721 形成共价键。 | |||
T27242 |
EF24
EF 24,EF-24,3,5-Bis[(2-fluorophenyl)Methylene]-4-piperidinone |
ERK; MEK; Caspase | Apoptosis; MAPK; Proteases/Proteasome |
EF24 (3,5-Bis[(2-fluorophenyl)Methylene]-4-piperidinone) 是姜黄素类似物,口服生物利用度高,抗肿瘤作用强。它可增强活化的 Caspase3 及 Caspase9 的水平,并抑制 MEK1 及 ERK 的磷酸化形式的表达。它可以抑制口腔鳞状细胞癌细胞的 MAPK/ERK 信号通路,从而发挥抗肿瘤作用。 | |||
T0850 |
Primaquine diphosphate
Primaquine phosphate,磷酸伯氨喹,Primaquine bisphosphate,磷酸伯安喹 |
Antibiotic; Parasite | Microbiology/Virology |
Primaquine diphosphate 是一种合成的 8-氨基喹啉衍生物,具有抗疟特性。它是一种能破坏间日疟原虫和卵形疟原虫肝脏晚期和潜在组织形态的化合物。 | |||
T60774 |
NITD-916
NITD916,NITD 916 |
Antibiotic | Microbiology/Virology |
NITD-916 是一种具有口服活性和高度亲脂性的分枝杆菌烯酰还原酶 InhA 抑制剂,IC50 为 570 nM。NITD-916是一种有有效的 4-羟基-2-吡啶酮衍生物, 与 InhA 和 NADH 形成三元复合物,阻止进入脂肪酰基底物结合袋。NITD-916 具有抗结核活性。 | |||
T21460 |
Teriparatide acetate
hPTH 1-34 (acetate salt),Parathar acetate,Forteo,醋酸立特帕肽 |
Others | Others |
Teriparatide acetate (Forteo) 是一种 PHT 激动剂,在 HEK293 细胞中的 IC50 为 2 nM。Teriparatide acetate 是一种重组形式的甲状旁腺激素。它是一种有效的合成代谢(即骨骼生长)剂,用于治疗某些形式的骨质疏松症。间歇使用特立帕肽比破骨细胞更能激活成骨细胞,从而导致骨骼整体增加。 | |||
T6929 |
Pantoprazole sodium
Pantecta,泮托拉唑钠盐,SKF96022 sodium,SKF96022 (sodium),BY1023 (sodium),泮托拉唑钠,BY-1023 sodium,Pantoloc |
Apoptosis; Others; Proton pump; HIF; Autophagy | Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; Membrane transporter/Ion channel; Others |
Pantoprazole sodium (Pantecta) 是一种具有口服活性的质子泵抑制剂,是一种取代的苯并咪唑,是H+/K+-ATPase 抑制剂,IC50为 6.8 μM。它可以改善 pH 值稳定性,具有抗分泌和抗溃疡的作用。它联合阿霉素可显著增加肿瘤生长延迟。 | |||
T22043 |
BCATc Inhibitor 2
|
Others | Others |
BCATc Inhibitor 2 是选择性分支链氨基转移酶抑制剂,可用于神经退行性疾病的研究。能够抑制 rBCATc (IC50:0.2 μM),hBCATc (IC50:0.8 μM)、 rBCATm (IC50:3.0 μM)。其中BCATc 也称为 BCAT1,存在于细胞质基质中的亚型。 | |||
T35856 |
BMS-986176
|
AAK1 (AP2 associated kinase 1) | Neuroscience |
BMS-986176 是一种有效的AAK1 抑制剂,IC50为 2.2 nM。BMS-986176在神经退行性疾病中有研究的价值。 | |||
T36587 |
8-Aminopyrene-1,3,6-trisulfonic Acid sodium salt
|
Others | Others |
8-Aminopyrene-1,3,6-trisulfonic Acid sodium salt 是一种阴离子荧光染料,用作葡萄糖传感和检测其他糖类的报告分子。激发/发射光谱为 425/503 nm。 它可以在溶液中使用,也可以通过还原胺化连接醛官能化单体来固定,而不会显著改变荧光强度。 | |||
T25937 |
Pepsinostreptin
N-Isobutyrylpepstatin |
||
Pepsinostreptin is a pepsin inhibitor that forms a 1:1 complex with pepsin and suppresses its activity. | |||
T31233 |
DDOH
p,p'-Ddoh,DDOM |
||
DDOH is a metabolite of DDT and forms conjugates with palmitic acid in DDT-treated female rats. | |||
T26463 |
A110
A-110,A 110 |
||
A110 is a potent and selective IMPDHs inhibitor. It binds to the NAD(+) cofactor site and forms a ternary complex with IMP. | |||
T39366 | Corixetan | ||
Corixetan is a potent thorium chelator that effectively forms stable complexes with Th-227 in vivo. | |||
T20725 |
Disodium nitrilotriacetate
Disodium hydrogen nitrilotriacetate,Kiresuto NTB |
||
Disodium nitrilotriacetate is used as a chelating agent, which forms coordination compounds with metal ions such as Fe3+, Cu2+, and Ca2+. | |||
T28135 |
NC043
NC 043,NC-043 |
||
NC043 is an inhibitor of Wnt/β-catenin signaling, it forms a covalent bond with the Cys-516 residue of CARF. | |||
T71336 |
CASP3 Activator 1541B
|
||
CASP3 Activator 1541B is an activator of the proenzyme forms of caspase-3, and is an inducer of cell death. | |||
T71894 |
AZD3229 Tosylate
|
||
AZD3229 Tosylate is a highly potent inhibitor targeting mutant forms of the pan-KIT enzyme, with a primary application in the treatment of gastrointestinal stromal tumors (GISTs). | |||
T36298 |
Tyrocidine Complex
|
||
Tyrocidine complex is a mixture of cyclic decapeptides originally isolated from B. brevis. It is active against Gram-positive and Gram-negative bacteria. It forms a complex with single- and double-stranded DNA to inhibit RNA synthesis. | |||
T36244 |
SJF 1521
|
||
Selective EGFR Degrader. Comprises the EGFR inhibitor lapatinib (Cat. No. 6811) joined by a linker to a von Hippel-Lindau (VHL) recruiting ligand. Exhibits selectivity for EGFR, including mutant forms, over HER2. Induces degradation of EGFR in OVCAR8 cells. | |||
T35677 |
2,3,4-Tri-O-acetyl-β-D-Glucuronide methyl ester
|
||
2,3,4-Tri-O-acetyl-β-D-glucuronide methyl ester is a synthetic intermediate in the synthesis of prodrug forms of the antitumor antibiotic daunomycin .1 1.Leenders, R.G.G., and Scheeren, H.W.Synthesis and evaluation of novel daunomycin-phosphate-sulfate-β-glucuronide and -β-glucoside prodrugs for application in ADEPTBioorg. Med. Chem. Lett.5(24)2975-2980(1995) |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3901 |
Solasonine
|
Others | Others |
Solasonine 是一种甾体糖苷生物碱,从龙葵中分离获得,对人胃癌细胞有细胞毒性。 | |||
T7970 |
7-Ethoxycoumarin
|
Others | Others |
7-Ethoxycoumarin 是细胞色素 P450(CYP) 的底物,现已被应用于多种 CYP 的功能表征。 | |||
T5S1550 |
Cinnamyl alcohol
肉桂醇,肉桂醇;beta-苯丙烯醇,Cinnamic Alcohol,Styryl Carbinol |
PPAR | DNA Damage/DNA Repair; Metabolism |
Cinnamyl alcohol (Styryl Carbinol) 是从板栗花中分离得到的一种活性成分,抑制增加的 PPARγ表达,具有抗肥胖作用。 | |||
T8293 |
γ-Tocopherol
D-gamma-生育酚,γ-生育酚,(+)-γ-Tocopherol |
COX | Immunology/Inflammation; Neuroscience |
γ-Tocopherol ((+)-γ-Tocopherol) 是有效的环氧合酶抑制剂,是存在于玉米油和大豆中的维生素 E,具有抗炎特性和抗癌活性。 | |||
T3322 |
trans-Chalcone
Chalcone,反-查耳酮,查尔酮,Cinnamophenone,Chalkone |
Apoptosis; Others; Antifungal; Fatty Acid Synthase | Apoptosis; Metabolism; Microbiology/Virology; Others |
trans-Chalcone (Chalkone) 是从 Aronia melanocarpa 果皮中分离出来的一种天然产物,是类黄酮前体的双酚核心结构。它是脂肪酸合酶和 α-淀粉酶的抑制剂,具有抗真菌和抗癌活性。 | |||
T0392 |
Artemisinin
Qinghaosu,Artemisinine,Qinghaosu,NSC 369397,青蒿素,Artemisinine |
HCV Protease; Ferroptosis; Akt; Parasite | Apoptosis; Cytoskeletal Signaling; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Artemisinin (Qinghaosu) 是一种倍半萜烯内酯,是从青蒿植物的地上部分分离的一种抗疟疾药物。它有神经保护和抗癌作用。 | |||
T2S0961 |
Chalcone
benzylideneacetophenone,phenyl styryl ketone,Cinnamophenone,benzalacetophenone,β-phenylacrylophenone,查耳酮 |
EGFR; Antibacterial | Angiogenesis; JAK/STAT signaling; Microbiology/Virology; Tyrosine Kinase/Adaptors |
Chalcone (Cinnamophenone) 是从甘草中分离得到的一种芳香酮,可合成查耳酮衍生物。它具有多种生物和药理的活性,如抗炎、抗菌、抗癌、抗氧化、抗寄生虫等活性。 | |||
T20113 |
D-(+)-Malic acid
(R)-Malic acid,Malic acid, D-,D-(+)-苹果酸,D-Malic acid |
Others | Others |
D-(+)-Malic acid ((R)-Malic acid) 一种是Malic acid 活性异构体,是竞争性的 L(--)malic acid 转运的抑制剂。 | |||
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。 | |||
T5528 |
Cyanidin Chloride
|
Antioxidant | oxidation-reduction |
Cyanidin Chloride 是一种花青素的亚类,具有抗氧化和抗癌活性。它能够抑制破骨细胞形成,羟基磷灰石吸收和 NF-κB 配体 (RANKL) 诱导的破骨细胞标记基因表达的受体激活。 | |||
TN6768 |
Amylopectin
|
Others | Others |
Amylopectin 是一种基于葡萄糖的高度支化的多糖。它与直链淀粉一起形成淀粉。支链淀粉的糖苷键为α-葡聚糖链α- 1、4和支链点α- 1,6。 | |||
T3121 |
Betulin
Trochol,betulinic alcohol,betuline,betulinol,桦木醇,Betulol,白桦脂醇 |
Apoptosis; Endogenous Metabolite; Lipid; Fatty Acid Synthase | Apoptosis; Metabolism |
Betulin (betulinol) 是从桦树树皮中分离出来的一种天然三萜,是 SREBP 抑制剂。 | |||
T16525 |
PhIP
|
Others | Others |
PhIP 是来源于熟肉的一种杂环芳香胺(HAA),属于吡啶类杂环胺,是2B 类致癌物,具有雌激素活性。PhIP 可与 DNA 形成加合物,从而促进癌症发生。 | |||
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。 | |||
T4916 |
D-Glucaric acid potassium
D-Saccharic acid potassium salt,Glucosaccharic acid,D-葡萄糖二酸单钾盐,Glucaric Acid |
Others; Endogenous Metabolite | Metabolism; Others |
D-Glucaric acid potassium (D-Saccharic acid potassium salt) 是内源性代谢产物的一种。 | |||
T5004 |
Hyaluronic acid sodium
透明质酸钠,Sodium Hyaluronate |
Others | Others |
Hyaluronic acid sodium (Sodium Hyaluronate) 是一种生物聚合物,由二糖的重复单元组成,应用领域广泛。 | |||
T2A2498 |
L-Lysine
Aminutrin,Lysine Acid,lysine,L-赖氨酸,赖氨酸 |
Virus Protease; Endogenous Metabolite; Antifection | Metabolism; Microbiology/Virology |
L-Lysine (Aminutrin) 是一种人类必需氨基酸,能增加钙吸收,减少糖尿病相关疾病和改善肠道健康,可用于疱疹的研究。 | |||
T5219 |
L-Alloisoleucine
L-别异亮氨酸,L-allo-Isoleucine,(3R)-LS-Isoleucine,L(+)-Alloisoleucine |
Others; Endogenous Metabolite | Metabolism; Others |
L-Alloisoleucine (L-allo-Isoleucine) 是 L-异亮氨酸的立体异构体,是一种支链氨基酸,是人血浆的常见成分 (尽管水平较低)。 | |||
T4776 |
Glycerol
Glycerin,甘油 |
Endogenous Metabolite | Metabolism |
Glycerol 是甘油三酯(即脂肪和油)和磷脂的重要成分。它在食品工业中被广泛用作甜味剂和保湿剂以及药物制剂。 | |||
T3794 |
Pentagalloylglucose
Penta-O-galloyl-β-D-glucose,1,2,3,4,6-O-Pentagalloylglucose,1,2,3,4,6-Penta-O-galloyl-beta-D-glucopyranose,1,2,3,4,6-五没食子酰葡萄糖 |
Influenza Virus | Microbiology/Virology |
1,2,3,4,6-O-Pentagalloylglucose (Penta-O-galloyl-β-D-glucose) 存在于多种植物中,具有重要的药理作用。Pentagalloylglucose 表现出显著的抗狂犬病病毒 (RABV) 活性。 | |||
TN4733 |
Pancixanthone A
胡桐,海棠木 |
Antifection | Microbiology/Virology |
Pancixanthone A may have antimalarial activity, it also shows a significant antileishmanial activity against the promastigote forms of Leishmania mexicana and L. infantum and against the amastigote forms of L. infantum. | |||
T40454 |
DMAPP
Dimethylallyl diphosphate |
||
DMAPP, also known as Dimethylallyl pyrophosphate, is an isoprenoid precursor found in all life forms. It serves as an isomer of isopentenyl pyrophosphate (IPP). | |||
T19565 | Streptolysin O | Others | Others |
Streptolysin O causes both lysis of cells and cardiotoxicity. Streptolysin O is widely used for the controlled permeabilization of cell membranes. Streptolysin O exists in two forms, a reduced active state and an oxidized reversibly inactive state . | |||
TN2515 |
1,7-Bis(4-hydroxyphenyl)hepta-4,6-dien-3-one
|
Antifection | Microbiology/Virology |
(4Z,6E)-5-hydroxy-1,7-bis(4-hydroxyphenyl)hepta-4,6-dien-3-one shows growth inhibitory activity in vitro versus bloodstream forms of African trypanosomes, with the IC(50) value in the range of 1-3 microg/mL. | |||
TN5872 |
Phebalosin
Alosin |
||
Phebalosin displays 50% effective concentrations (EC(50)) of 14.1 microg/mL against axenic amastigote forms of Leishmania panamensis. It also displays cytotoxicity (IC(50)) at concentrations of 20.7 microg/mL on human promonocytic U-937 cells. | |||
T39168 |
Epsilon-(gamma-glutamyl)-lysine
Epsilon-(gamma-glutamyl)-lysine,γ-Glu-ε-Lys,H-Glu(H-Lys-OH)-OH |
||
Epsilon-(gamma-glutamyl)-lysine is an N(6)-acyl-L-lysine derivative that forms bonds between extracellular matrix (ECM) components with the assistance of the enzyme tissue transglutaminase (tTg). These bonds are implicated in the pathogenesis of certain diseases like non-diabetic kidney and glaucoma filtration. | |||
T0937 |
Riboflavin
Vitamin B2,维生素B2,E101 |
Endogenous Metabolite | Metabolism |
Riboflavin (E101),一种人内源性代谢物, 是极易吸收的微量营养素。 | |||
TN5404 |
(+)-Conocarpan
|
||
Conocarpan has antinociceptive effects. Conocarpan is quite active against S. aureus and B. subtilis with MIC of 6.25 micrograms/ml, it also shows activity against M. tuberculosis (MIC=15.6 ug/ml). Conocarpan shows considerable activity against epimastigo | |||
T77242 | Pectin | ||
Pectin是从高等植物细胞壁中提取的一种杂多糖。作为纳米颗粒制备,它用作活性分子的运载载体。此外,Pectin还具有吸附剂和广谱抗菌剂的功能,能够结合肠道粘膜中的细菌毒素及其他刺激物,从而缓解受刺激的黏膜。 | |||
T36439 |
Gramicidin A
|
Antibacterial; HIF; Parasite | Angiogenesis; Chromatin/Epigenetic; Microbiology/Virology |
Gramicidin A 是一种从从 B. brevis 分离出来的多肽类抗生素。Gramicidin A 是一种高度疏水的通道形成离子载体,在人工膜中形成一价阳离子可渗透的通道。Gramicidin A 诱导缺氧诱导因子 1α (HIF-1α) 的降解,并能降低人肾细胞癌小鼠异种移植模型的生长。Gramicidin A 具有抗菌、抗疟活性以及溶血活性。 |