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  • T222491588-A4ARS-1620 Intermediate

    1588-A4 is an intermediate of ARS-1620 which is an atropisomeric selective KRASG12C inhibitor with desirable pharmacokinetics.

    价 格：￥电议型 号：T22249产 地：中国大陆

  • T20331Sodium lauroyl glutamateHostapon CLG；Amisoft LS 11；Acylglutamate LS-11；Sodium N-lauroylglutamate

    Sodium lauroyl glutamate is derived from glutamic acid, lauric acid, and sodium. It is used as a gentle cleanser more suitable for sensitive skin.

    价 格：￥电议型 号：T20331产 地：中国大陆

  • T19562Polyethylene glycol 12-hydroxystearateSolutol HS-15

    Solutol HS-15 is a permeability enhancer.

    价 格：￥电议型 号：T19562产 地：中国大陆

  • T1894IdelalisibCAL-101；GS-1101；艾代拉里斯

    Idelalisib is a small molecule inhibitor of the PI3K catalytic subunit p110δ (IC50: 2.5 nM). The selectivity for p110δ is 40- to 300-fold than p110α/β/γ.

    价 格：￥电议型 号：T1894产 地：中国大陆

  • T17042TES-1025

    TES-1025 is an effective and selective inhibitor of human α-amino-β-carboxymuconate-ε-semialdehyde decarboxylase (IC50: 13 nM).

    价 格：￥电议型 号：T17042产 地：中国大陆

  • T16994PimitespibTAS-116

    TAS-116 is an ATP-competitive and highly specific HSP90α/HSP90β inhibitor (Kis: 34.7 nM and 21.3 nM, respectively).

    价 格：￥电议型 号：T16994产 地：中国大陆

  • T16798RS 17053 hydrochlorideRS-17053

    RS 17053 hydrochloride is an effective and selective antagonist of α1A-adrenergic receptor with pA2 of 9.8 in functional assays and pKi of 9.1 in the native cell membrane.

    价 格：￥电议型 号：T16798产 地：中国大陆

  • T1615Irbesartan厄贝沙坦；SR-47436；BMS-186295

    Irbesartan is an Angiotensin 2 Receptor Blocker. The mechanism of action of irbesartan is as an Angiotensin 2 Receptor Antagonist.

    价 格：￥电议型 号：T1615产 地：中国大陆

  • T16136MRS-1706

    MRS-1706 has Ki values of 1.39, 112, 157, and 230 nM for human A2B, A2A, A1, and A3 receptors respectively. MRS-1706 is an effective and selective adenosine A2B receptor inverse agonist.

    价 格：￥电议型 号：T16136产 地：中国大陆

  • T14991CMS-121CMS121

    CMS-121, a quinolone derivative, is an orally active acetyl-CoA carboxylase 1 (ACC1) inhibitor. CMS-121 protects HT22 cells against ischemia and oxidative damage (EC50: 7 nM and 200 nM). CMS-121 shows strong neuroprotective, antioxidative, anti-inflammato

    价 格：￥电议型 号：T14991产 地：中国大陆

  • T14765BOS-172722

    BOS-172722 is an inhibitor of monopolar spindle 1 (MPS1) checkpoint(IC50 of 2 nM).

    价 格：￥电议型 号：T14765产 地：中国大陆

  • T13145Thiazolidinone-Derivatives-1

    Thiazolidinone-Derivatives-1 is an agent of antiulcer,and inhibits the secretion of gastric acid.

    价 格：￥电议型 号：T13145产 地：中国大陆

  • T13108PamufetinibTAS-115；H2OL3Q4XRD；4-(2-Fluoro-4-(3-(2-phenylacetyl)thioureido)phenoxy)-7-methoxy-N-methy

    TAS-115 is a potent inhibitor of VEGFR and hepatocyte growth factor receptor (c-Met/HGFR)-targeted kinase(IC50s of 30 and 32 nM for rVEGFR2 and rMET, respectively).

    价 格：￥电议型 号：T13108产 地：中国大陆

  • T12478LPinacidilP1134；S 1230；P 1134；P-1134；S-1230

    Pinardil (P-1134, S-1230) is a guanidine that opens potassium channels and directly dilates peripheral blood vessels in small arteries, lowering blood pressure and peripheral resistance and producing fluid retention.

    价 格：￥电议型 号：T12478L产 地：中国大陆

  • T10566BMS-191095

    BMS-191095 is mitochondrial ATP-sensitive potassium (mitoKATP) channel activator.

    价 格：￥电议型 号：T10566产 地：中国大陆

  • T10565BMS-1001 hydrochloride

    BMS-1001 hydrochloride is an orally active inhibitor of human PD-1/PD-L1 immune checkpoint with low-toxicity in cells.BMS-1001 alleviates the inhibitory effect of the soluble PD-L1 on the T-cell receptor-mediated activation of T-lymphocytes. BMS-1001 is c

    价 格：￥电议型 号：T10565产 地：中国大陆

  • T10376ARS-1630

    ARS-1630 is a mutant K-ras G12C inhibitor extracted from patent WO 2015054572 A1. It is a less active enantiomer of ARS-1620.

    价 格：￥电议型 号：T10376产 地：中国大陆

  • T10375ARS-1323

    ARS-1323 is the racemate of ARS-1620 and a mutant K-ras G12C inhibitor.

    价 格：￥电议型 号：T10375产 地：中国大陆

  • T10374ARS-1323-alkyne

    ARS-1323-alkyne is a switch-II pocket (S-IIP) inhibitor and a conformational specific chemical reporter of KRASG12C nucleotide state in living cells.

    价 格：￥电议型 号：T10374产 地：中国大陆

  • T10255AES-135

    AES-135 is a potent HDAC inhibitor, inhibits HDAC3, HDAC6, HDAC11 (IC50s: 654, 190, and 636 nM) with anti-tumor activity.

    价 格：￥电议型 号：T10255产 地：中国大陆

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