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  • T15335FN-1501

    FN-1501 is a potent FLT3 and CDK inhibitor (IC50s: 2.47, 0.85, 1.96, and 0.28 nM for CDK2/cyclin A, CDK4/cyclin D1, CDK6/cyclin D1 and FLT3, respectively). FN-1501 also has anticancer activity.

    价 格：￥电议型 号：T15335产 地：中国大陆

  • T1533Valganciclovir hydrochloride缬更昔洛韦盐酸盐；Valcyt；Valcyte；Valganciclovir HCl

    Valganciclovir Hydrochloride is a hydrochloride salt form of valganciclovir, a prodrug form of ganciclovir, a nucleoside analog of 2´-deoxyguanosine, with antiviral activity. After phosphorylation, valganciclovir is incorporated into DNA, resulting in inh

    价 格：￥电议型 号：T1533产 地：中国大陆

  • T15324Fmoc-NH-PEG8-NHS esterFMOC-N-酰氨基-DPEG(R)8-NHS酯

    Fmoc-NH-PEG8-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

    价 格：￥电议型 号：T15324产 地：中国大陆

  • T1532Pidotimod

    Pidotimod is a synthetic dipeptide with immunomodulatory properties.

    价 格：￥电议型 号：T1532产 地：中国大陆

  • T1531Mometasone furoate糠酸莫美他松；糠酸莫米松；Sch32088

    Mometasone furoate is a pregnadienediol derivative ANTI-ALLERGIC AGENT and ANTI-INFLAMMATORY AGENT that is used in the management of ASTHMA and ALLERGIC RHINITIS. It is also used as a topical treatment for skin disorders.

    价 格：￥电议型 号：T1531产 地：中国大陆

  • T15304Fmoc-8-amino-3,6-dioxaoctanoic acid[2-[2-(Fmoc-氨基)乙氧基]乙氧基]乙酸；Fmoc-NH-PEG2-CH2COOH

    Fmoc-8-amino-3,6-dioxaoctanoic acid is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). It is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.

    价 格：￥电议型 号：T15304产 地：中国大陆

  • T15300FluorofenidoneAKF-PD

    Fluorofenidone attenuates the progression of renal interstitial fibrosis partly by suppressing NADPH oxidase and extracellular matrix (ECM) deposition via the PI3K/Akt signalling pathway. Fluorofenidone is an analogue of AMR69. Which displays equivalent l

    价 格：￥电议型 号：T15300产 地：中国大陆

  • T1530Mitiglinide calcium hydrate米格列奈钙；S-21403 calcium hydrate；KAD-1229 calcium hydrate；Mitiglinide calciu

    Mitiglinide calcium dihydrate is a drug for the treatment of type 2 diabetes. Mitiglinide is thought to stimulate insulin secretion by closing the ATP-sensitive K(+) K(ATP) channels in pancreatic beta-cells. Mitiglinide belongs to the meglitinide class of

    价 格：￥电议型 号：T1530产 地：中国大陆

  • T12323ORM-15341

    ORM-15341 is a potent and full antagonist for human AR (hAR)( with IC50 values of 38 nM as shown by transactivation assays in AR-HEK293 cells)

    价 格：￥电议型 号：T12323产 地：中国大陆

  • T11539HCV-IN-29

    HCV-IN-29 is a hepatitis C virus (HCV) inhibitor.

    价 格：￥电议型 号：T11539产 地：中国大陆

  • T11538Hck-IN-1

    Hck-IN-1 is a selective Nef-dependent Hck inhibitor (IC50s: 2.8 μM and >20 μM for Nef:Hck complex and Hck) with antiretroviral activity. Hck-IN-1 is a direct and wide HIV-1 Nef antagonist with an IC50 of 100-300 nM for wild-type HIV-1 replication.

    价 格：￥电议型 号：T11538产 地：中国大陆

  • T11533HA155CS-963

    HA155 selectively and potently inhibits autotaxin with an IC50 of 5.7 nM.

    价 格：￥电议型 号：T11533产 地：中国大陆

  • T1153Trimethoprim甲氧苄啶；NIH 204；BW 56-72；NSC-106568

    Trimethoprim is a Dihydrofolate Reductase Inhibitor Antibacterial. The mechanism of action of trimethoprim is as a Dihydrofolate Reductase Inhibitor, and Cytochrome P450 2C8 Inhibitor, and Organic Cation Transporter 2 Inhibitor.

    价 格：￥电议型 号：T1153产 地：中国大陆

  • T10718LCCT241533 hydrochloride

    CCT241533 hydrochloride is an effective and selective ATP competitive inhibitor of CHK2 (Ki: 1.16 nM; IC50: 3 nM).

    价 格：￥电议型 号：T10718L产 地：中国大陆

  • T0153OltiprazRP 35972；NSC 347901；吡噻硫酮

    Oltipraz is a synthetic dithiolethione with potential chemopreventive and anti-angiogenic properties. Oltipraz induces phase II detoxification enzymes, such as glutathione S transferase (GST) and NAD(P)H: quinone oxidoreductase 1 (NQO1). The induction of

    价 格：￥电议型 号：T0153产 地：中国大陆

  • T0153OltiprazOltipraz,NSC 347901,RP 35972

    Oltipraz is a synthetic dithiolethione with potential chemopreventive and anti-angiogenic properties. Oltipraz induces phase II detoxification enzymes, such as glutathione S transferase (GST) and NAD(P)H: quinone oxidoreductase 1 (NQO1). The induction of

    价 格：￥电议型 号：T0153产 地：美洲

  • T10718LCCT241533 hydrochlorideCCT241533 hydrochloride

    CCT241533 hydrochloride is an effective and selective ATP competitive inhibitor of CHK2 (Ki: 1.16 nM; IC50: 3 nM).

    价 格：￥电议型 号：T10718L产 地：美洲

  • T11153EG00229EG00229

    EG00229 selectively inhibits VEGF-A binding to NRP1 b1 domain with an IC50 of 3 μM, but has no effect on VEGFA binding to VEGFR-1 and VEGFR-2. EG00229 is a neuropilin 1 (NRP1) receptor antagonist.

    价 格：￥电议型 号：T11153产 地：美洲

  • T1153TrimethoprimTrimethoprim,BW 56-72,NIH 204

    Trimethoprim is a Dihydrofolate Reductase Inhibitor Antibacterial. The mechanism of action of trimethoprim is as a Dihydrofolate Reductase Inhibitor, and Cytochrome P450 2C8 Inhibitor, and Organic Cation Transporter 2 Inhibitor.

    价 格：￥电议型 号：T1153产 地：美洲

  • T11530H3B-6545 HydrochlorideH3B-6545 Hydrochloride

    H3B-6545 Hydrochloride is an ?selective, oral estrogen receptor covalent antagonist (SERCA).?

    价 格：￥电议型 号：T11530产 地：美洲

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