92
21
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T38117 |
WSP-5
Washington State Probe-5,WSP-5 |
||
Hydrogen sulfide (H2S) is an important gaseous mediator, like nitric oxide, that has significant effects on the immunological, neurological, cardiovascular and pulmonary systems of mammals. WSP-5 is a reactive disulfide-containing, fluorescent probe designed for fast detection of H2S in biological samples and cells. Through a reaction-based fluorescent turn-on strategy, WSP-5 selectively and rapidly reacts with H2S, generating a fluorophore with excitation and emission maxima of 502 and 525 nm, ... | |||
T7414 |
ARS-853
|
Apoptosis; Raf; Ras | Apoptosis; GPCR/G Protein; MAPK |
ARS-853 是一种选择性共价KRAS G12C 抑制剂,IC50为 2.5 μM。它通过与 GDP 结合的癌蛋白结合并阻止激活来抑制突变 KRAS 驱动的信号传导。 | |||
T22675 |
Co 102862
V 102862 |
Others; Sodium Channel | Membrane transporter/Ion channel; Others |
Co 102862 是一种电压门控钠通道阻滞剂。 Co 102862 可用于抗惊厥的研究。 | |||
T10826 |
CK-666
|
HIV Protease; Microtubule Associated | Cytoskeletal Signaling; Microbiology/Virology; Proteases/Proteasome |
CK-666 是一种肌动蛋白相关蛋白 Arp2/3 复合物的细胞渗透性抑制剂。 它与 Arp2/3 复合物结合,稳定复合物的非活性状态,阻止 Arp2 和 Arp3 亚基进入活化的丝状短节距构象。 | |||
T8369 |
Adagrasib
MRTX849 |
Ras | GPCR/G Protein; MAPK |
Adagrasib (MRTX849) 是一种 KRAS G12C 共价抑制剂,具有口服活性和选择性。Adagrasib 与 KRAS G12C 非活性构象的 GDP 状态结合,抑制 KRAS 及其下游信号的传导。Adagrasib 对 KRAS G12C 突变肿瘤具有抑制活性。 | |||
T12519 |
Sodium metatungstate
POM-1,聚钨酸钠,Sodium polyoxotungstate |
Phosphatase | Metabolism |
Sodium metatungstate (Sodium polyoxotungstate) 是一种外核苷三磷酸二磷酸水解酶抑制剂,能够抑制 ATP 的分解,并阻断中枢突触传递,这是独立于抑制 NTPDase 而发挥作用的。 | |||
T64830 | Tetrapotassium decatungstate | ||
Tetrapotassium decatungstate 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T64830。 | |||
T64838 | Tetrabutylphonium decatungstate | ||
Tetrabutylphonium decatungstate 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T64838。 | |||
T30154 |
Ascorbyl myristate
Ascorbyl monomyristate,6-tetradecanoate,L-Ascorbic acid |
||
Ascorbyl myristate is a bioactive chemical. | |||
T33791 |
Oleyl myristate
|
||
Oleyl myristate is a bioactive chemical. | |||
T64775 | Sodium tungstate(VI) | ||
Sodium tungstate(VI) 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T64775。 | |||
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. | |||
T64579 | Tetrabutylammonium decatungstate | ||
Tetrabutylammonium decatungstate 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T64579。 | |||
T80552 |
Prostate Specific Antigen Substrate
|
||
Prostate Specific Antigen Substrate为前列腺特异性抗原(PSA)的荧光底物,专用于检测PSA的酶活性。 | |||
T21339 |
Peramivir
RWJ 270201,BCX1812,BCX 1812,帕拉米韦,RWJ270201 |
||
Peramivir, a neuraminidase inhibitor, acts as a transition-state analogue inhibitor of influenza neuraminidase and thereby preventing new viruses from emerging from infected cells. It is used as an antiviral drug for the treatment of influenza. | |||
T5370 |
DTT
二硫苏糖醇,DL-Dithiothreitol |
Others | Others |
DTT (DL-Dithiothreitol) 是一种强还原剂。它被氧化后,会形成带有内部二硫键的稳定六元环。 | |||
T13925 |
THS-044
N-[2-Nitro-4-(Trifluoromethyl)phenyl]morpholin-4-Amine,N-Morpholino-2-nitro-4-(trifluoromethyl)aniline |
HIF | Angiogenesis; Chromatin/Epigenetic |
THS-044 (N-[2-Nitro-4-(Trifluoromethyl)phenyl]morpholin-4-Amine) 的结合可稳定 HIF2α PAS-B 折叠状态,kd 为 2 μM,并在内源性和临床环境中调节 HIF2 活性。 | |||
T8700 |
TKIM
|
Potassium Channel | Membrane transporter/Ion channel |
TKIM 是一种 TWIK 相关的钾通道 1 (TREK-1) 抑制剂,与 TREK-1 的中间 (IM) 状态的口袋结合。 | |||
T21769L |
β-Pompilidotoxin Acetate
β-Pompilidotoxin Acetate(216064-36-7 Free base) |
Sodium Channel | Membrane transporter/Ion channel |
β-Pompilidotoxin Acetate 是一种黄蜂毒肽。 它可以减缓钠通道的失活并增加细胞中的稳态钠电流。 | |||
T15711 |
Larazotide acetate
|
Gap Junction Protein | Cytoskeletal Signaling |
Larazotide acetate 是合成肽,它起到紧密连接调节器的作用,并将泄漏连接反转到它们的常闭状态。 | |||
T19352 |
HBC620
|
Others | Others |
HBC620 在 Pepper 结合状态下显示出明亮的荧光,可以可视化活细胞中的 RNA 动力学。 HBC620 是一种类似 HBC 的荧光团。 | |||
T26287 |
Transcainide
R54718,R 54718,R-54718 |
Sodium Channel | Membrane transporter/Ion channel |
Transcainide(R 54718) 是一种新的利多卡因类似物,是具有口服活性的抗心律失常剂。Transcainide 可阻断牛心脏和大鼠骨骼肌中 BTX 激活的钠通道的开放状态。 | |||
T2635 |
Org 27569
|
Cannabinoid Receptor | GPCR/G Protein |
Org 27569 是一种 CB1 receptor 别构调节剂,可以增加激动剂与 CB1 结合,能够抑制激动剂诱导的 CB1 信号通路。 | |||
T2169 |
Zebularine
NSC309132,4-Deoxyuridine |
DNA Methyltransferase; Autophagy | Autophagy; Chromatin/Epigenetic |
Zebularine (4-Deoxyuridine) 是一种 DNA 甲基化抑制剂,还抑制胞苷脱氨酶。它通过以共价水合物的形式与活性大小结合,充当胞苷脱氨酶的过渡态类似物抑制剂。 | |||
T29037 |
UC-781
NSC 675186,UC781,UC 781 |
Antiviral; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
UC-781 (NSC-675186) 是一种高效且具有选择性的人类免疫缺陷病毒 HIV-1 非核苷类逆转录酶(NNRTI)I抑制剂 ,C50 值为 5 nM。UC-781 具有抗病毒活性和耐药性。UC-781状态稳定,较低的 PH 或不同温度对其影响较小。 | |||
T8711 |
PF-05186462
PF-05150122 |
Sodium Channel | Membrane transporter/Ion channel |
PF-05186462 (PF-05150122)是选择性的人Nav1.7电压依赖性钠通道抑制剂,IC50为 21 nM,与其他钠通道 (Nav 1.1、1.2、1.3、1.4、1.5、1.6 和 1.8) 相比,它对 Nav1.7显示出显著的选择性。PF-05186462在急性或慢性疼痛中具有研究价值。 | |||
T33816 |
Ordopidine
ACR-325,ACR 325,ACR325 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Ordopidine (ACR325) 是一种多巴胺能稳定剂,可抑制精神刺激剂引起的多动症,并在不活动时刺激行为。Ordopidine 在体外作为多巴胺 D2 受体拮抗剂起作用,尽管亲和力低,但其依赖于特定状态的行为效应特征是 D2 受体拮抗剂所不具备的。 | |||
T8684 |
Sotorasib
AMG-510 |
Ras | GPCR/G Protein; MAPK |
Sotorasib (AMG-510) 是一种 KRAS G12C 共价抑制剂,具有口服活性和选择性。Sotorasib 与 KRAS G12C 非活性构象的 GDP 状态结合,抑制 KRAS 及其下游信号的传导。Sotorasib 对 KRAS G12C 突变肿瘤具有抑制活性。 | |||
T24754 |
Hh-Ag1.5
SAG-1.5,SAG1.5,SAG 1.5 |
Hedgehog/Smoothened | GPCR/G Protein; Stem Cells |
Hh-Ag1.5 (SAG-1.5) 是一种高效的 Hedgehog (Hh) 激动剂(EC50: 1 nM)和Smoothened (Smo)受体激动剂,对Smo的 EC50 为 1 nM、 Ki值在 0.5 和 2.3 nM 之间。Hh-Ag1.5 介导的重编程打破了非损伤肝脏干细胞的静止状态,从而挽救了肝衰竭。Hh-Ag1.5 诱导 hiPSCs 分化为皮肤前体细胞、脊髓运动神经元和脊髓感觉神经元。 | |||
T13983 |
0990CL
|
cAMP; Others | GPCR/G Protein; Others |
0990CL 是一种有效的异三聚体Gαi subunit 特异性抑制剂,可与纯化的Go±在gdp 结合状态下相互作用,能够阻断α2AR 介导的cAMP 调控。 在细胞模型中低浓度0990CL 能够部分恢复cAMP 水平,高浓度的0990CL (10 μM)下,开始对细胞活力产生负面影响。 | |||
T9972 |
Divarasib
GDC-6036 |
Ras | GPCR/G Protein; MAPK |
Divarasib (GDC-6036) (GDC-6036)是一种正在研究的、口服的、高效力和选择性的 KRAS G12C 抑制剂,IC50 为 <0.01 μM。Divarasib 不可逆地将 KRAS G12C 癌蛋白锁定在非活性状态,抑制肿瘤细胞生长。它正在被研究用于实体肿瘤,包括非小细胞肺癌和结肠直肠癌及其他类型的癌症。 | |||
T2408 |
Ostarine
MK-2866,GTX-024,Enobosarm |
Androgen Receptor | Endocrinology/Hormones |
Ostarine (MK-2866) 是一种具有合成代谢活性的非甾体药物。选择性雄激素受体调节剂 (SARM) GTx-024 旨在像睾酮一样发挥作用,从而促进和/或维持性欲、生育能力、前列腺生长以及肌肉生长和力量。模仿睾酮的作用,这种药物可以增加瘦体重,从而改善癌症恶病质高代谢状态下的肌肉萎缩。 | |||
T14884 |
CBR-5884
|
Others; Dehydrogenase | Metabolism; Others |
CBR-5884 是一种磷酸甘油酸脱氢酶抑制剂,IC50为 33 μM。 它抑制癌细胞中的丝氨酸合成,选择性地抑制黑素瘤和乳腺癌细胞系的增殖,对具有高丝氨酸生物合成活性的癌细胞系有选择性毒性。 | |||
T37807 |
JTV 519 fumarate
|
||
Ryanodine receptor (RyR) inhibitor; stabilizes RyR2 in a closed conformation. Exhibits antiarrhythmic and cardioprotective properties in vivo. Hunt et al (2007) K201 (JTV519) suppresses spontaneous Ca2+ release and [3H]ryanodine binding to RyR2 irrespective of FKBP12.6 association. Biochem.J. 404 431 PMID:17313373 |Chen et al (2008) Effect of K201, a novel antiarrhythmic drug on calcium handling and arrhythmogenic activity of pulmonary vein cardiomyocytes. Br.J.Pharmacol. 153 915 PMID:17994112 |... | |||
T24902 |
TROX-1
TROX1,TROX 1 |
||
TROX-1 is the activation state-dependent Cav2 channel antagonist. | |||
T14992 |
Raxatrigine hydrochloride
GSK-1014802 hydrochloride,CNV1014802 (hydrochloride) |
Others | Others |
Raxatrigine hydrochloride is a state-dependent sodium channel blocker and a Nav1.7 sodium channel inhibitor. | |||
T30827 |
Cgp 33304
Cgp-33304,Cgp33304 |
||
CGP 33304 is a dual leukotriene receptor antagonist and phospholipase A2 inhibitor. It prevents hypoxia secondary to bronchial constriction induced by leukotriene in a shocking state. | |||
T25896 |
Octicidine
ASOHO |
||
Octicidine is derived from phaseolotoxin by the removal of C-terminal dipeptide. It is a transition state analog that irreversibly suppresses ornithine carbamoyltransferase. | |||
T25184 |
Butalamine
Butalamina |
||
Butalamine is a vasodilator (peripheral) with local anesthetic effects. It suppresses state 3 respiration and decreases ADP/O in the rat liver. | |||
T34665 |
SN-1
SN1 |
||
SN-1 is a zinc chelator which increases steady-state expression level of A3G in the presence of Vif. | |||
T81459 |
Pinacyanol iodide
|
||
Pinacyanol iodide,一种具有超快激发态异构化特性的荧光花青染料。 | |||
T25184L |
Butalamine HCl
LA 1221,Hemotrope,Butalamine hydrochloride,Adrevil |
||
Butalamine HCl is a vasodilator (peripheral) with local anesthetic effects. It suppresses state 3 respiration and decreases ADP/O in the rat liver. | |||
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。 | |||
T71239 |
CNV-2197944
|
||
CNV-2197944 is a novel, small molecule, state-dependent calcium channel blocker, designed to selectively inhibit highly active Cav2.2 channels. | |||
T70543 |
U 92163
|
||
U 92163 is synthetic peptidic transition state analog inhibitor that was used to determine the crystallographic structure of the protease from human immunodeficiency virus type 2. | |||
T7352L |
Pridopidine hydrochloride
ASP2314 HCl,Pridopidine HCl,FR310826,ASP-2314 hydrochloride |
||
Pridopidine Hydrochloride is a dopaminergic stabilizer that has been shown to improve a variety of neurological and psychiatric disorders, including Huntington's disease. Pridopidine Hydrochloride stabilizes psychomotor activity in a state-dependent way t | |||
T23506 | Viomycin | Others | Others |
Viomycin is a member of the tuberactinomycin family of antibiotics. Viomycin also inhibits group I intron splicing and prokaryotic protein synthesis. Freezes bacterial ribosomes in either the pre- or post-translational state. Facilitates trans-cleavage of | |||
T19351 |
HBC599
|
Others | Others |
HBC599 is an HBC-like fluorophore. HBC599 shows brightly fluoresced in the Pepper bound state and can be visualized RNA dynamics in live cells. | |||
T10374 | ARS-1323-alkyne | Ras | GPCR/G Protein; MAPK |
ARS-1323-alkyne 是switch-II pocket (S-IIP)抑制剂,能够特异性报告活体细胞中 KRASG12C 核苷酸的状态。 | |||
TP1977 |
187-1, N-WASP inhibitor
|
||
Inhibits neural Wiskott-Aldrich syndrome protein (N-WASP) by stabilizing the autoinhibited state of the protein. Blocks phosphatidylinositol 4,5-bisphosphate (PIP2)-stimulated actin assembly (IC50 ~ 2 μM) but does not directly inhibit actin polymerization |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TQ0198 |
Phorbol 12-myristate 13-acetate
佛波醇12-十四酸酯13-乙酸酯,PMA |
NF-κB; S1P Receptor; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; GPCR/G Protein; NF-κB |
Phorbol 12-myristate 13-acetate (PMA) 属于佛波酯类天然产物,是一种 PKC、SphK、NF-κB 的激活剂。Phorbol 12-myristate 13-acetate 可诱导 THP1 细胞分化。 | |||
T20005 |
Isopropyl myristate
IPM,Isomyst,HSDB 626,肉豆蔻酸异丙酯,FEMA No. 3556,十四酸异丙酯,NSC 406280,Stepan D-50 |
Others | Others |
Isopropyl myristate (IPM) 是异丙醇和肉豆蔻酸的酯。它是一种可用于化妆品和外用药物制剂中的极性润肤剂。 | |||
TN6901 |
Methyl myristate
肉豆蔻酸甲酯,methyl tetradecanoate |
Others | Others |
Methyl myristate (methyl tetradecanoate) 是一种肉豆蔻酸经酯化反应得到的饱和脂肪酸甲酯。对 B16F10 黑色素瘤具有显著的诱导作用。 | |||
T8040 |
Cholesterol myristate
胆甾烯基豆蔻酸酯,Cholesteryl myristate,胆固醇肉豆蔻酸,Cholesteryl tetradecanoate |
Others; Potassium Channel; GABA Receptor; Endogenous Metabolite; AChR | Membrane transporter/Ion channel; Metabolism; Neuroscience; Others |
Cholesterol myristate (Cholesteryl myristate) 是粗吻海龙中的一种类固醇,可与多种离子通道结合,例如nAChR、GABAA 受体和内向整流钾离子通道。 | |||
TN6994 |
Ethyl Myristate
|
||
Ethyl Myristate is a natural product. | |||
TN4546 |
Methyl isocostate
|
Others | Others |
Methyl isocostate 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 TN4546,CAS号为 132342-55-3。 | |||
T10023 |
1-Naphthol
NSC 9586,Nako TRB,1-萘酚,Furro ER |
Endogenous Metabolite | Metabolism |
1-Naphthol (Furro ER) 是激发态质子转移荧光分子探针。 | |||
T4884 |
alpha-D-glucose
α-D-Glucose,α-葡萄糖,alpha-Glucose,α-Dextrose |
Others; Endogenous Metabolite | Metabolism; Others |
alpha-D-glucose (α-Dextrose) 是内源性代谢产物的一种。 | |||
T0887 |
D-Glucose
Dextrose,D-无水葡萄糖,Glucopyranose,Grape sugar,葡萄糖,D(+)-Glucose |
Endogenous Metabolite | Metabolism |
D-Glucose (Glucopyranose) 是一种单糖。D-Glucose 是甜味剂,是一般代谢的关键组成部分,并作为与细胞代谢状态以及生物和非生物应激反应有关的关键信号分子。 | |||
T8733 |
Antrodin A
(2-氯苯基)二苯基甲醇,camphorataanhydride A |
Others | Others |
Antrodin A (camphorataanhydride A) 是固体发酵樟脑菌菌丝体的一种主要活性成分。它能够增强肝脏的抗炎及抗氧化能力,维持肠道菌群的稳定,避免酒精对肝脏的损伤。 | |||
T67685 |
4-Methylumbelliferyl-β-D-xylopyranoside
4-Methylumbelliferyl-β-D-xyloside |
||
4-Methylumbelliferyl-β-D-xylopyranoside (4-Methylumbelliferyl-β-D-xyloside)在生物实验中展现出爆裂的稳态动力学,这支持底物4-Methylumbelliferyl-β-D-xylopyranoside 糖苷键快速水解的结论。4-Methylumbelliferyl-β-D-xylopyranoside 可用于 β- 木糖苷酶活性研究。 | |||
T2910 |
Flavonol
3-羟基黄酮,3-Hydroxyflavone,3-HF,Flavon-3-ol,3-Hydroxy-2-phenylchromone |
Others; Endogenous Metabolite | Metabolism; Others |
Flavonol (3-Hydroxyflavone) 是内源性代谢产物的一种。 | |||
TN1163 |
2'-Hydroxychalcone
|
Others | Others |
2'-Hydroxychalcone 是一种药物合成中间体,可用于合成黄酮类化合物。负载在纳米乳液中的2'-Hydroxychalcone 在Danio rerio 模型对副球孢子菌显示出杀真菌活性。2'-Hydroxychalcone 通过负载脂质的Hepg2细胞中的氧化应激诱导细胞毒性。2'-Hydroxychalcone 抑制通过逆转录聚合酶链反应确定的肿瘤坏死因子-α诱导ICAM-1,VCAM-1和E-选择素的稳态转录水平,因此可能会干扰其基因的转录。 | |||
T38108 |
Fulvic Acid
|
Antioxidant; PDE | Metabolism; oxidation-reduction |
Fulvic Acid 是一种来自土壤、沉积物或水生环境中微生物产生的腐殖质的天然产物,是一种首次青霉菌中分离出的酚酸和真菌代谢产物。Fulvic Acid 抑制淀粉样蛋白b (17-42) (AB17-42)二聚化,破坏预先形成的AB17-42三聚体,并结合到磷酸二酯酶5A (PDE5A)的催化位点,可以调节机体免疫系统,影响细胞的氧化状态,改善胃肠功能。Fulvic Acid 可作为氧化剂或还原剂, 具有研究糖尿病等慢性炎症性疾病的潜力。 | |||
T38395 | Pyrrole-2-carboxaldehyde | ||
Pyrrole-2-carboxaldehyde exhibits distinctive vibrational and electronic properties which serve to validate its dimeric state in the solid phase and monomeric state in the solution phase. | |||
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 . | |||
TN2830 | 26-Nor-8-oxo-alpha-onocerin | Others | Others |
26-Nor-8-oxo-alpha-onocerin can promote the osteoblast proliferation rate, the effect is time-dependent,concentration-dependent and differentiation state-dependent. | |||
TN3844 |
Didrovaltrate
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Didrovaltrate shows cytotoxic against human cancer cell lines. Didrovaltrate blocks I(Ca-L) in a concentration-dependent manner and probably inhibits I(Ca-L) in its inactive state, which may contribute to its cardiovascular effect. | |||
TN1912 |
Marinobufogenin
南美蟾毒精,Marinobufagenin |
ATPase; EGFR | Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
Marinobufagenin, a cardiotonic steroid, its increased concentrations are important in the cardiac disease and oxidant stress state seen with renal failure. | |||
T71750 | Quinolactacin A1 | ||
Quinolactacin A1 是一种有效的乙酰胆碱酯酶 (AChE) 抑制剂,可从Penicillium citrinum 中得到。Quinolactacin A1 可用于阿尔茨海默病的研究。 | |||
TN3541 |
Broussonin E
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ERK; p38 MAPK; TNF; JAK; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling; MAPK; Stem Cells |
Broussonin E could suppress inflammation by modulating macrophages activation state via inhibiting the ERK and p38 MAPK and enhancing JAK2-STAT3 signaling pathway, and can be further developed as a promising drug for the treatment of inflammation-related |