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  • T8819SU-9516SU 9516,SU9516

    SU9516 is a selectively potent ATP-competitive inhibitor of CDKs.

    价 格：￥电议型 号：T8819产 地：中国大陆

  • T19058Solvent Yellow 16Solvent Yellow 16

    Solvent Yellow 16, a disperse dye, is a coloring agent in cosmetics.

    价 格：￥电议型 号：T19058产 地：美洲

  • T4975SM 16SM 16

    SM 16 is a ALK5/ALK4 kinase inhibitor (Ki: 10/1.5 nM).

    价 格：￥电议型 号：T4975产 地：美洲

  • T6167SU9516SU9516

    SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also has inhibitory effects on CDK1 and CDK4, with IC50s of 40 nM and 200 nM, respectively.

    价 格：￥电议型 号：T6167产 地：美洲

  • T8819SU-9516；化合物SU-9516SU-9516

    SU9516 is a selectively potent ATP-competitive inhibitor of CDKs.

    价 格：￥电议型 号：T8819产 地：中国大陆

  • T79659SARS-CoV-2 3CLpro-IN-16；SARS-CoV-2 3CLpro 抑制剂16SARS-CoV-2 3CLpro-IN-16

    SARS-CoV-2 3CLpro-IN-16 is a covalent SARS-CoV-2 3CLpro inhibitor that inhibits 3CLpro activity and achieves its inhibitory effect by forming a covalent bond with Cys145.

    价 格：￥电议型 号：T79659产 地：中国大陆

  • T79412SHP2-IN-16；化合物 SHP2-IN-16SHP2-IN-16

    SHP2-IN-16 (compound 222) is a potent SHP2 inhibitor exhibiting an IC50 of 1 nM, and is applicable in glioblastoma research [1].

    价 格：￥电议型 号：T79412产 地：中国大陆

  • T79258sEH inhibitor-16；化合物 sEH inhibitor-16sEH inhibitor-16

    sEH Inhibitor-16, a potent soluble epoxide hydrolase (sEH) inhibitor, exhibits an IC50 of 2 nM. It diminishes inflammatory damage associated with cerulein-induced acute pancreatitis (AP) in mice, making it suitable for inflammation and immunology research [1].

    价 格：￥电议型 号：T79258产 地：中国大陆

  • T79183SOS1-IN-16；化合物 SOS1-IN-16SOS1-IN-16

    SOS1-IN-16 (Comp 54) serves as a selective SOS1 inhibitor exhibiting an IC50 value of 7.2 nM and demonstrates inhibitory activity against CYP3A4 with an IC50 of 8.9μM when testosterone is employed as a substrate. This compound is utilized in cancer research [1].

    价 格：￥电议型 号：T79183产 地：中国大陆

  • T78425GK16S；化合物 GK16SGK16S

    GK16S, a UCHL1 chemogenomic probe, serves as a complementary tool to GK13S for the investigation of UCHL1 function in cellular studies [1].

    价 格：￥电议型 号：T78425产 地：中国大陆

  • T78033SDP116；化合物 SDP116SDP116

    SDP116, a synthetic peptide derivative of the GPR116 Stachel sequence, exhibits ADGRF5 agonistic activity [1].

    价 格：￥电议型 号：T78033产 地：中国大陆

  • T70946SC 51316；化合物 SC 51316SC 51316

    SC 51316 is a nonpeptidic angiotensin II (AII) receptor antagonist.

    价 格：￥电议型 号：T70946产 地：中国大陆

  • T64990(2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-10,13-Dimethyl-2,16-di(piperidin-1-yl)hexadecahydro-1H-cyclopen

    (2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-10,13-Dimethyl-2,16-di(piperidin-1-yl)hexadecahydro-1H-cyclopenta[a]phenanthrene-3,17-diol is a useful organic compound for research related to life sciences. The catalog number is T64990 and the CAS number is 13522-16-2.

    价 格：￥电议型 号：T64990产 地：中国大陆

  • T6167SU9516；化合物SU9516SU9516

    SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also has inhibitory effects on CDK1 and CDK4, with IC50s of 40 nM and 200 nM, respectively.

    价 格：￥电议型 号：T6167产 地：中国大陆

  • T60757SB-216；化合物SB-216SB-216

    SB-216 is able to be used for the research of cancer which is a potent inhibitor of tubulin polymerization. SB-216 exhibits strong antiproliferative potency in a panel of human cancer cell lines, including melanoma, breast cancer, and lung cancer [1].

    价 格：￥电议型 号：T60757产 地：中国大陆

  • T60556SARS-CoV-2-IN-16；化合物 SARS-CoV-2-IN-16SARS-CoV-2-IN-16

    SARS-CoV-2-IN-16 (Compound 12) is a potent inhibitor of SARS-CoV-2 nucleocapsid protein (NPro) with potent antiviral activity (EC50 = 3.69 μM). SARS-CoV-2-IN-16 binds to NPro with a low Kd value of 7.82 μM, which suggests that SARS-CoV-2-IN-16 is an effective NPro ligand [1].

    价 格：￥电议型 号：T60556产 地：中国大陆

  • T4975SM 16；化合物SM 16SM 16

    SM 16 is a ALK5/ALK4 kinase inhibitor (Ki: 10/1.5 nM).

    价 格：￥电议型 号：T4975产 地：中国大陆

  • T4516Sitsirikine；化合物 T4516Sitsirikine

    Sitsirikine is a natural product from Catharanthus roseus.

    价 格：￥电议型 号：T4516产 地：中国大陆

  • T39800S2116；S2116S2116

    S2116 is a powerful inhibitor of lysine-specific demethylase 1 (LSD1), and it is a derivative of N-alkylated tranylcypromine (TCP). S2116 exhibits its inhibitory effects by increasing H3K9 methylation and inducing reciprocal H3K27 deacetylation at super-enhancer regions. In TCP-resistant T-cell acute lymphoblastic leukemia (T-ALL) cells, S2116 triggers apoptosis by repressing the transcription of NOTCH3 and TAL1 genes. Furthermore, S2116 demonstrates significant growth retardation of T-ALL cells

    价 格：￥电议型 号：T39800产 地：中国大陆

  • T35674StRIP16；StRIP16StRIP16

    Rab8a GTPase-binding stapled peptide (Kd = 12.7 μM). Cell permeable; localizes to the endomembrane system.

    价 格：￥电议型 号：T35674产 地：中国大陆

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