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  • T72437PARP1/2/TNKS1/2-IN-1；PARP1/2/TNKS1/2抑制剂1PARP1/2/TNKS1/2-IN-1

    PARP1/2/TNKS1/2-IN-1 is a multi-target inhibitor of PARP-1, PARP-2, TNKS1 and TNKS2.PARP1/2/TNKS1/2-IN-1 has potential anti-tumor activity and induces apoptosis.

    价 格：￥电议型 号：T72437产 地：中国大陆

  • T72242DYRKs-IN-1 hydrochloride；化合物 DYRKs-IN-1 hydrochlorideDYRKs-IN-1 hydrochloride

    DYRKs-IN-1 hydrochloride is a potent inhibitor of Dual-specificity tyrosine-phosphorylation-regulated kinases (DYRKs), exhibiting IC50 values of 5 nM and 8 nM for DYRK1A and DYRK1B, respectively. This compound demonstrates antitumor activity.

    价 格：￥电议型 号：T72242产 地：中国大陆

  • T72032PI5P4Ks-IN-2；化合物PI5P4Ks-IN-2PI5P4Ks-IN-2

    PI5P4Ks-IN-2 is an inhibitor of the phosphatidylinositol 5-phosphate 4-kinase PI5P4Kγ. Targeting the PI5P4K isoforms, PI5P4Ks-IN-2 inhibited PI5P4Kα, PI5P4Kβ, PI5P4Kγ, and PI5P4Kγ+, with IC50 values of <4.3, <4.6, 6.2, and 0.32, respectively.

    价 格：￥电议型 号：T72032产 地：中国大陆

  • T71549RKS-262；化合物 RKS-262RKS-262

    RKS262 is a specific cyclin/CDK inhibitor. RKS262 was identified by structural optimization of Nifurtimox which is currently undergoing phase II clinical trials to treat high-risk neuroblastoma. In a NCI(60) cell-line assay RKS262 exhibited significant cytotoxicity in ovarian cancer cells and a variety of other cell lines exceeding effects of commercial drugs such as cisplatin, 5-FU, cyclophosphamide or sapacitabine. Various leukemia cell-lines were most sensitive (GI(50):?~?10 nM) while several

    价 格：￥电议型 号：T71549产 地：中国大陆

  • T71013KS I；化合物 KS IKS I

    KS I is a gonadotropin antagonist and is a cyclolignan isolated from extracts of Lycopus and Lithosperum after oxidation with caffeic acid.

    价 格：￥电议型 号：T71013产 地：中国大陆

  • T70934KS99；化合物 KS99KS99

    KS99 is a dual inhibitor of BTK and tubulin polymerization.

    价 格：￥电议型 号：T70934产 地：中国大陆

  • T70788KST012174 HCl；化合物 KST012174 HClKST012174 HCl

    KST012174 is a HIF-1α inhibitor. KST012174 involves in the HIF-1α/p300 protein?protein interaction.

    价 格：￥电议型 号：T70788产 地：中国大陆

  • T70103KSK213；化合物 KSK213KSK213

    KSK213 is a potent inhibitor of Chlamydia trachomatis Infectivity (EC50 = 60 nM). KSK213 potently inhibited multiple serovars of C. trachomatis while not affecting the growth of key species from the commensal flora or host cell viability at 25 μM.

    价 格：￥电议型 号：T70103产 地：中国大陆

  • T69146Suksdorfin；化合物 SuksdorfinSuksdorfin

    Suksdorfin has hypoglycemic effects, promotes adipocyte differentiation and enhances lipocalin production, activates peroxisome proliferator-activated receptor gamma (PPARγ), promotes insulin-dependent glucose uptake by adipocytes, and can be used to study obesity.

    价 格：￥电议型 号：T69146产 地：中国大陆

  • T64665DiAzKs hydrochloride；化合物 DiAzKs hydrochlorideDiAzKs hydrochloride

    DiAzKs hydrochloride is a useful organic compound for research related to life sciences and the catalog number is T64665.

    价 格：￥电议型 号：T64665产 地：中国大陆

  • T63992KS100；化合物 KS100KS100

    KS100 is a selective and potent ALDH inhibitor with antiproliferative and anticancer activities.KS100 inhibits ALDH1A1, ALDH2 and ALDH3A1 with IC50 of 334, 2137 and 360 nM, respectively.KS100 promotes apoptosis and induces cell-cycle arrest, which can be used to study colon cancer.

    价 格：￥电议型 号：T63992产 地：中国大陆

  • T63081KS106；化合物 KS106KS106

    KS106 is a selective and potent ALDH inhibitor with antiproliferative and anticancer activity, inhibits ALDH1A1, ALDH2, and ALDH3A1 with IC50 of 334, 2137, and 360 nM, respectively.KS106 contributes to apoptosis, induces an increase in G2/M cell cycle arrest, and can be used to study melanoma and colon cancer.

    价 格：￥电议型 号：T63081产 地：中国大陆

  • T61339LDHA/PDKs-IN-1；化合物 LDHA/PDKs-IN-1LDHA/PDKs-IN-1

    LDHA/PDKs-IN-1 (compound 20e) is a highly effective dual inhibitor of PDKs and LDHA, displaying IC50 values of 0.8 μM and 0.15 μM, respectively. It significantly suppresses A549 cell proliferation (EC50 = 13.2 μM), reduces lactate formation, and enhances oxygen consumption. This compound holds great promise for cancer research [1].

    价 格：￥电议型 号：T61339产 地：中国大陆

  • T60995LDHA/PDKs-IN-2；化合物 LDHA/PDKs-IN-2LDHA/PDKs-IN-2

    LDHA/PDKs-IN-2 (compound 20k) is a potent LDHA and PDKs dual inhibitor with IC50 values of 0.7 and 1.6 μM, respectively. LDHA/PDKs-IN-2 increases oxygen consumption as well as decreases the lactate formation. LDHA/PDKs-IN-2 shows the potential for the cancer research which reduces the proliferation of A549 cell with an EC 50 of 15.7 μM [1].

    价 格：￥电议型 号：T60995产 地：中国大陆

  • T60982PI5P4Ks-IN-1；化合物 PI5P4Ks-IN-1PI5P4Ks-IN-1

    PI5P4Ks-IN-1 (compound 7) is an active compound which engages PI5P4Kγ[1].

    价 格：￥电议型 号：T60982产 地：中国大陆

  • T60039KSQ-4279；化合物KSQ-4279USP1-IN-1；USP1-IN-1

    KSQ-4279 (USP1-IN-1) is an inhibitor of USP1 and PARP.KSQ-4279 has anticancer activity and is used in the study of non-small cell lung cancer, osteosarcoma, ovarian, breast, glioblastoma, bladder, uterine and pancreatic cancers.

    价 格：￥电议型 号：T60039产 地：中国大陆

  • T4760KSD 2405；3-羟基苯甲醇3-Hydroxybenzyl alcohol；3-羟基苯甲醇|||3-Hydroxybenzyl alcohol

    KSD 2405 (3-Hydroxybenzyl alcohol) is a hydroxybenzyl alcohol that is phenol substituted at position C-3 by a hydroxymethyl group. It is a pink or beige to brown crystalline powder, soluble in water.

    价 格：￥电议型 号：T4760产 地：中国大陆

  • T39704KSC-34；化合物 KSC-34KSC-34

    KSC-34 is a covalent modifier of protein disulfide isomerase A1 (PDIA1).KSC-34 is a selective inhibitor targeting the a-site of PDIA1.It inhibits PDIA1 reductase activity in a time-dependent manner and is used to study diseases caused by abnormalities in amyloid.CAS ??128-63-63-5

    价 格：￥电议型 号：T39704产 地：中国大陆

  • T39205HKSOX-1；HKSOX-1HKSOX-1

    HKSOX-1 is a fluorescent probe which is used for imaging and detection of endogenous superoxide in live cells and in vivo. HKSOX-1 exhibits excellent selectivity and sensitivity towards superoxide anion radical.

    价 格：￥电议型 号：T39205产 地：中国大陆

  • T39014KSPWFTTL；KSPWFTTLKSPWFTTL

    KSPWFTTL is an immunodominant epitope derived from the p15E transmembrane protein. It is Kb-restricted and can enhance the susceptibility of a tumor cell line to cytotoxic T lymphocytes targeting anti-AKR/Gross MuLV.

    价 格：￥电议型 号：T39014产 地：中国大陆

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