76
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3700 |
SCH900776 (S-isomer)
MK-8776 S-isomer,SCH900776 S-isomer |
Chk; CDK | Cell Cycle/Checkpoint |
SCH900776 S-isomer (MK-8776 S-isomer) 是SCH900776的S 型同分异构体。 | |||
T60196 |
IHMT-PI3Kδ-372 S-isomer
|
PI3K | PI3K/Akt/mTOR signaling |
IHMT-PI3Kδ-372 S-isomer 是一种有效的选择性 PI3Kδ 抑制剂,IC50 为 14 nM。IHMT-PI3Kδ-372 S-isomer 对 PI3Kδ 的选择性高于其他 I 类 PI3K (56-83 倍) 和其他蛋白激酶。IHMT-PI3Kδ-372 S-isomer 可用于慢性阻塞性肺疾病 (COPD )的研究。 | |||
T63166L |
(S, R)-LSN 3318839
(S, R)-LSN 3318839(Isomer-2764704-18-7) |
Glucagon Receptor | GPCR/G Protein |
T30261 |
AZD6482 (S-isomer)
AZD-6482,AZD 6482,AZD6482 (S),AZD6482 |
||
AZD6482 (S-isomer) is a potent, selective, ATP-competitive PI3Kβ inhibitor (IC(50) 0.01 μm), which can inhibit insulin-induced in vitro glucose uptake by human adipocytes (IC(50) is 4.4 μm). | |||
T19571 |
T3-ATA (S-isomer)
|
Others | Others |
T3-ATA S-isomer, the S-isomer of T3-ATA, represents the active form of the thyroid hormone. | |||
T19572 |
T4-ATA (S-isomer)
|
Others | Others |
T4-ATA S-isomer, the active form of the thyroid hormone, represents the S-isomer of T4-ATA. | |||
T29007 |
Trichostatin A S-isomer
(-)-Trichostatin A |
||
Trichostatin A S-isomer is the s-isomer of Trichostatin A. Trichostatin A is a histone deacetylase inhibitors (HDIs or HDACIs) that have a broad spectrum of epigenetic activities. Trichostatin A inhibits HDACs 1, 3, 4, 6 and 10 with IC50 values around 20 | |||
T27933 |
LY243246
LY249543 disodium,LY249543 sodium,LY 249543,LY-249543,S-isomer of lometrexol,DB04322,LY249543 |
||
LY249543, the S-isomer of lometrexol, is an inhibitor of Methylenetetrahydrofolate Dehydrogenase/Cycl. | |||
T10545 |
BIO-32546
|
PDE | Metabolism |
BIO-32546 (S-isomer) 是一种高效的 autotaxin (ATX) 的调节剂,IC50 值为 1 nM。 | |||
T12644L |
(S)-Thalidomide
(S)-(-)-Thalidomide |
Apoptosis | Apoptosis |
(S)-Thalidomide ((S)-(-)-Thalidomide) 是 Thalidomide 的 S 型异构体,具有免疫调节,抗炎,抗癌,抗血管生成活性和促凋亡活性,可用于研究麻风结节性红斑和骨髓瘤。 | |||
T22420 |
(S)-Viloxazine Hydrochloride
(S)-Viloxazine HCl |
Norepinephrine | Neuroscience |
(S)-Viloxazine Hydrochloride 是Viloxazine 的S 异构体。Viloxazine 是一种选择性去甲肾上腺素再摄取抑制剂(NRI),可用作抗抑郁药。 | |||
T50052 |
1,2-diphenylpropan-2-amine
|
Others | Others |
1,2-diphenylpropan-2-amine 是Remacemide 的(S,R)-异构体单盐酸盐代谢产物。1,2-diphenylpropan-2-amine 具有抗惊厥作用。 | |||
T20626 |
Esomeprazole
|
Proton pump; Cysteine Protease | Membrane transporter/Ion channel; Proteases/Proteasome |
Esomeprazole 是奥美拉唑(omeprazole) 的S-异构体,抑制溶酶体半胱氨酸蛋白酶legumain,防止癌症转移。它是一种质子泵抑制剂(PPI)。 | |||
T0785 |
Dexchlorpheniramine Maleate
S-(+)-Chlorpheniramine maleate salt,右泛醇,马来酸右氯苯那敏 |
Dopamine Receptor; 5-HT Receptor; Norepinephrine; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Dexchlorpheniramine Maleate (S-(+)-Chlorpheniramine maleate salt) 是一种具有抗胆碱能特性的抗组胺药,用于治疗花粉热或荨麻疹等过敏性疾病。 | |||
T60224 |
1H-Pyrrolo[2,1-c][1,2,4]benzothiadiazine, 2,3,3a,4-tetrahydro-, 5,5-dioxide, (3aR)-
|
GluR | Neuroscience |
1H-Pyrrolo[2,1-c][1,2,4]benzothiadiazine, 2,3,3a,4-tetrahydro-, 5,5-dioxide, (3aR)-是S 18986的低活性异构体。S 18986是一种AMPA 受体阳性调节剂,EC2(浓度为AMPA 诱导电流强度的两倍)为35μM。 | |||
T2686L |
Esomeprazole Sodium
埃索美拉唑钠,(S)-Omeprazole sodium |
ATPase; Proton pump | Membrane transporter/Ion channel |
Esomeprazole Sodium ((S)-Omeprazole sodium) 是一种口服有效的活性质子泵抑制剂。Esomeprazole sodium 通过抑制胃壁细胞中的 H+, K+-ATPase 来降低酸分泌,在胃食管反流疾病中有研究价值。Esomeprazole 是一种外泌体抑制剂,通过抑制 V-H+-ATPases 来阻断外泌体的释放。 | |||
T2686 |
Esomeprazole Magnesium
(S)-Omeprazole magnesium,NEXIUM,埃索美拉唑镁,(-)-Omeprazole magnesium |
ATPase; Proton pump | Membrane transporter/Ion channel |
Esomeprazole Magnesium (NEXIUM) 是一种口服有效的 H+, K+-ATPase 抑制剂,在上消化道疾病和胃食管反流疾病中具有研究价值。Esomeprazole magnesium 是一种外泌体抑制剂,通过抑制 V-H+-ATPases 来阻断外泌体的释放。 | |||
T13252L |
(S)-Rasagiline mesylate
TVP1022 (mesylate),(S)-雷沙吉兰甲磺酸,S-PAI mesylate |
Others | Others |
(S)-Rasagiline mesylate is rasagiline S-isomer, and is an agent of anti-Parkinson. | |||
T13252 |
(S)-Rasagiline
TVP1022,(S)-雷沙吉兰,S-PAI |
Others | Others |
(S)-Rasagiline is rasagiline S-isomer, and is an agent of anti-Parkinson. | |||
T71319 |
Alpiropride, (S)-
|
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Alpiropride, (S)-, is the S isomer of Alpiropride --- a dopamine antagonist. | |||
T70780 |
BW 737C89
|
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BW 737C89 is a highly potent dopamine D1 receptor antagonist; BW-737C is the (S)-isomer; BW-736C is the (R)-isomer. | |||
T21271 |
(S)-AMPA
L-AMPA, S-AMPA |
||
(S)-AMPA is an active isomer of AMPA and a selective agonist of AMPA. | |||
T19612 |
(2S)-Octyl-α-hydroxyglutarate
(2S)-Octyl-2-HG |
Others | Others |
(2S)-Octyl-α-hydroxyglutarate ((2S)-Octyl-2-HG) is a S-isomer 2-Hydroxyglutarate modified form. | |||
T12801 |
(S)-IDO1-IN-5
|
Others | Others |
(S)-IDO1-IN-5 is an active S-isomer of IDO1-IN-5. (S)-IDO1-IN-5 binds to IDOL(IC50 value less than 1.5 µΜ). | |||
T13869 |
Ribocil B
Ribocil S enantiomer,ent-Ribocil A |
Others | Others |
Ribocil-B is the active S-isomer of ribocil which can inhibit flavin mononucleotide (FMN,KD of 6.6 nM). | |||
T13452 |
(S)-MCPG
(+)-MCPG |
Others | Others |
(S)-MCPG is the active isomer of (RS)-MCPG, non-selective group I/group II metabotropic glutamate receptor antagonist. | |||
T31177 |
Dabelotine, (S)-
UNII-494Y55877B |
||
Dabelotine, (S)- 是 Dabelotine 的 S 型异构体。Dabelotine 是一种肾上腺素能受体激动剂,可用于研究痴呆症。 | |||
T70757 |
8-Acetyl-2-(dipropylamino)tetralin
|
||
8-Acetyl-2-(dipropylamino)tetralin is a 5-HT(1A) receptor agonist; both isomers are active, but the (S)-isomer is the most potent. | |||
T69453 |
APC-0576
|
||
APC-0576 is an (S,S)-isomer which inhibits NF-kappaB-dependent gene activation. APC-0576 may prevent pro-inflammatory cytokine-induced chemokine production in human endothelial cells. | |||
T25416 |
Fenvalerate
Evercide 2362 |
||
Fenvalerate is used as an insecticide. It is a mixture of four optical isomers which have different insecticidal activities. The 2-S alpha (or SS) configuration, known as esfenvalerate, is the most insecticidally active isomer. There is about 23% this iso | |||
T73802 | (S,S)-J-113397 | ||
(S,S)-J-113397 是 J-113397 的异构体。J-113397 是一种阿片类受体 (Opioid Receptor) 拮抗剂。 | |||
T13980 |
(S)-Gossypol (acetic acid)
(S)-(+)-Gossypol acetic acid,(S)-Gossypol acetic acid |
Others | Others |
(S)-Gossypol acetic acid is the isomer of a natural product Gossypol. | |||
T25669 |
Lercanidipine, (S)-
(S)-Lercanidipine,(+)-Lercanidipine |
||
Lercanidipine, (S)-是 Lercanidipine 的异构体,一种降压化合物。Lercanidipine 是二氢吡啶类的钙通道阻滞剂,具有持久的降压作用和肾脏保护作用。 | |||
T38148 |
(S)-KT109
(S)-KT109 |
||
(S)-KT109 is the (S) isomer of the diacylglycerol lipase β (DAGLβ) inhibitor KT109 . (S)-KT109 is a less potent inhibitor of DAGLβ (IC50 = 39.81 nM), DAGLα-mediated hydrolysis of 1-stearoyl-2-arachidonoyl-sn-glycerol (IC50 = 794.3 nM), and α/β-hydrolase domain-containing protein 6 (ABHD6; IC50 = 630.9 nM) than (R)-KT109 . | |||
T71889 |
Esoxybutynin Chloride
|
||
Esoxybutynin Chloride is (S)-enantiomer of oxybutynin. Esoxybutynin Chloride exerts antimuscarinic properties. Racemic oxybutynin is used clinically to treat urinary incontinence. Sepracor was developing (S)-oxybutynin, a single-isomer version of Alza's Ditropan (racemic oxybutynin), a muscarinic acetylcholine receptor antagonist, as a potential treatment for urinary incontinence. | |||
T83925 |
(S)-(–)-Deoxyarbutin
|
||
(S)-(–)-Deoxyarbutin是deoxyarbutin的异构体,具有酪氨酸酶抑制作用,在74 µM的浓度下可抑制酪氨酸酶活性。 | |||
T37227 |
(±)8(9)-DiHET
|
||
Epoxide hydrolases convert the EETs into vicinal diols, with the concurrent loss of much of their biological activity. The 8(S),9(R)-EET isomer is metabolized by platelet COX to form 8(S),9(R),11(R)-THETA, a trihydroxy fatty acid which may act as a renal vasoconstrictor. | |||
T71268 |
Esoxybutynin Free Base
|
||
Esoxybutynin Free Base is (S)-enantiomer of oxybutynin. Esoxybutynin Free Base exerts antimuscarinic properties. Racemic oxybutynin is used clinically to treat urinary incontinence. Sepracor was developing (S)-oxybutynin, a single-isomer version of Alza's Ditropan (racemic oxybutynin), a muscarinic acetylcholine receptor antagonist, as a potential treatment for urinary incontinence. | |||
T72753 |
RSV604 racemate
A-60444 racemate |
||
RSV604 (A-60444) racemate 是一种外消旋混合物,与 S-异构体相比,RSV604 racemate 对呼吸道合胞病毒(RSV)菌株的作用效果弱很多。 | |||
T37654 |
5(S)-HETE lactone
|
||
5(S)-HETE lactone is a cyclic ester formed by acid-catalyzed nucleophilic addition of the C-5 hydroxyl to the C-1 carboxyl of 5(S)-HETE. The ability of (±)5-HETE lactone to inhibit rat basophilic leukemia cell 5-lipoxygenase (IC50 = 27 μM) may be entirely due to the 5(S) isomer, but the enantiomers have not been tested separately. | |||
T72971 |
(S)-JDQ-443
(S)-NVP-JDQ443 |
||
(S)-JDQ-443 是 JDQ-443的异构体。JDQ-443 是一种口服有效和选择性的共价 KRAS G12C 抑制剂。JDQ-443 具有抗肿瘤活性。 | |||
T83828 |
Sp-2'-Deoxycytidine-5'-O-(1-thiotriphosphate) sodium
Sp-dCTP-α-S |
||
Sp-2'-Deoxycytidine-5'-O-(1-thiotriphosphate) (Sp-dCTP-α-S) 是含硫核苷酸衍生物 dCTP-α-S 的异构体。它抑制解氧核苷酸三磷酸三磷酸水解酶 SAMHD1(Ki = 6.3 µM)。 | |||
T63390 |
(S,S)-TAPI-1
|
||
(S,S)-TAPI-1 是一种 TAPI-1 的异构体。其中 TAPI-1是金属蛋白酶 (MMP) 抑制剂,也是 TACE(ADAM17) 抑制剂,对多种细胞表面蛋白脱落表现出有效的抑制作用。 | |||
T68523 |
AMG-628, (S)-
|
||
AMG-628, (S)-, is the S isomer of AMG-628 --- a potent, ATP-competitive inhibitor of Raf kinases. AMG-628 displays selectivity for Raf kinases and inhibits activation of tyrosine protein kinases such as VEGFR2, Lyn, Flt1 and Fms. AMG-628 has shown to inhibit growth, and induces cell cycle arrest and apoptosis in colon and melanoma cell lines with the B-RafV600E mutation. | |||
T83837 |
Rp-Thymidine-5'-O-(1-thiotriphosphate) sodium
Rp-dTTP-α-S |
||
Rp-Thymidine-5'-O-(1-thiotriphosphate) (Rp-TTP-α-S) 是含硫核苷酸衍生物 TTP-α-S 的一个异构体。它能与HIV-1逆转录酶结合(在镁、锰酸盐和钴存在下的Kds分别为45.7、27.32和39.44 µM)。 | |||
T72809 |
(S)-Renzapride
(S)-BRL 24924 |
||
(S)-Renzapride ((S)-BRL 24924) 是 Renzapride 的异构体。Renzapride 是一种 5-HT4受体激动剂,Ki 值为 115 nM。Renzapride 还是一种5HT2b 和5HT3受体拮抗剂。Renzapride 可用于便秘型肠易激综合征(C-IBS)的研究。 | |||
T37460 |
Lipoxin B4
Lipoxin B4 |
||
Lipoxin B4 (LXB4) is a positional isomer of LXA4 produced by the metabolism of 15-HETE or 15(S)-HpETE by human leukocytes. At a concentration of 100 nM, LXB4 inhibits polymorphonuclear leukocyte (PMN) migration stimulated by leukotriene B4 and inhibits LTB4-induced adhesion of PMNs with an IC50 value of 0.3 nM. | |||
T83834 |
Sp-Guanosine-5'-O-(1-thiotriphosphate) sodium
Sp-GTP-α-S,GTPαS(Sp),GTPαS(A) |
||
Sp-Guanosine-5'-O-(1-thiotriphosphate) (Sp-GTP-α-S) 是一种含硫核苷酸衍生物GTP-α-S的异构体。它能结合到微管蛋白上,在20 mM的浓度下用于无细胞实验时可诱导微管组装。 | |||
T36840 |
(R)-Omeprazole (sodium salt)
|
||
(R)-Omeprazole is the inactive isomer of omeprazole , a gastric proton-pump inhibitor. A stereoselective hydroxylation of (R)-omeprazole is mediated primarily by cytochrome P450 (CYP) 2C19, whereas CYP3A4 favors sulfoxidation of the active (S)-enantiomer . (R)-Omeprazole has been shown to act as a reversible direct-acting and metabolism-dependent inhibitor of CYP2C19 in pooled human liver microsomes (IC50 = 8.1 μM). | |||
T36562 |
(5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-ynoic Acid
|
||
(5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-ynoic acid is a stable isomer of 15(S)-HETE , a major arachidonic acid metabolite from the 15-lipoxygenase pathway. (5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-ynoic acid elicits concentration-dependent contraction of isolated pulmonary arteries from rabbits and inhibits the proliferation and migration of hormone-independent prostate carcinoma PC-3 cells. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4765 |
L-Norleucine
(S)-Norleucine,alpha-Aminocaproic acid,(S)-2-Aminohexanoic acid,L-2-氨基己酸 |
Influenza Virus; Endogenous Metabolite | Metabolism; Microbiology/Virology |
L-Norleucine ((S)-Norleucine) 是亮氨酸的异构体,特异性影响骨骼肌中的蛋白质合成,具有抗病毒活性。 | |||
T0493 |
L-Tyrosine
Tyrosine,P-Tyrosine,L-酪氨酸,L-p-Tyrosine,(S)-Tyrosine,酪氨酸 |
Amino Acids and Derivatives; Endogenous Metabolite | Metabolism |
L-Tyrosine ((S)-Tyrosine) 是一种非必需氨基酸,对后部皮层中柠檬酸合成酶具有抑制活性。 |