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  • T6071ParbendazoleSKF 29044;帕苯咪唑

    Parbendazole is a potent inhibitor of microtubule assembly(EC50 : 8.79 nM).Parbendazole is a carbamate ester-amine. It finds applications in control or treatment of nematode infestations.

    价 格:¥电议型 号:T6071产 地:中国大陆

  • T6066SCH772984

    SCH 772984 is a potent inhibitor of ERK1/ERK2 (IC50: 4/1 nM) and has only weak inhibitory for other 300 tested kinases.

    价 格:¥电议型 号:T6066产 地:中国大陆

  • T6029ONX-0914ONX 0914;PR-957;ONX0914

    ONX-0914 is an effective and specific immunoproteasome inhibitor, which has minimal cross-reactivity for the constitutive proteasome.

    价 格:¥电议型 号:T6029产 地:中国大陆

  • T6018Zosuquidar trihydrochloride唑喹达三盐酸盐;RS 33295-198 (D06387) 3HCl;Zosuquidar (LY335979) 3HCl;LY-335979 t

    Zosuquidar (LY335979) is a potent modulator of P-glycoprotein-mediated multi-drug resistance with Ki of 60 nM. Phase 3.

    价 格:¥电议型 号:T6018产 地:中国大陆

  • T60005WAY-296817

    WAY-296817 is casein kinase 1 (CK1) inhibitor and can be used for research on the treatment or prevention of diseases associated with circadiantiazol rhythm, inflammation diseases.

    价 格:¥电议型 号:T60005产 地:中国大陆

  • T5S2129Sciadopitysin

    Sciadopitysin may prevent the development of diabetic osteopathy, it exerts its therapeutic effects via upregulation of mitochondrial biogenesis.Sciadopitysin shows protective effects on antimycin A-induced toxicity in osteoblastic MC3T3-E1 cells, it may

    价 格:¥电议型 号:T5S2129产 地:中国大陆

  • T5S10283,29-Dibenzoyl Rarounitriol

    3,29-Dibenzoyl karounitriol is a natural product from Trichosanthes kirilowii Maxim.

    价 格:¥电议型 号:T5S1028产 地:中国大陆

  • T5829H4 Receptor antagonist 1

    H4 Receptor antagonist 1 is a potent and selective histamine H4 receptor inverse agonist, with an IC50 of 19 nM.

    价 格:¥电议型 号:T5829产 地:中国大陆

  • T5729L-quebrachitolL-白雀木醇;(-)-白雀木醇

    L-quebrachitol is a natural product.L-quebrachitol may promote osteoblastogenesis by triggering the BMP-2-response as well as the Runx2, MAPK, and Wnt/β-catenin signaling pathway.

    价 格:¥电议型 号:T5729产 地:中国大陆

  • T5675Almonertinib hydrochloride盐酸阿美替尼;HS-10296 hydrochloride

    HS-10296 hydrochloride is a small molecule inhibitor of EGFR-activating mutations and T790M-resistant mutation with limited activity against wild-type EGFR.

    价 格:¥电议型 号:T5675产 地:中国大陆

  • T56292-tert-Butyl-4-ethylphenol

    价 格:¥电议型 号:T5629产 地:中国大陆

  • T5533MC180295(rel)-MC180295

    MC180295 is a novel potent, highly selective CDK9 inhibitor (IC50: 5 nM), displays >22-fold selectivity over other CDKs.

    价 格:¥电议型 号:T5533产 地:中国大陆

  • T5464JNJ-10229570JNJ10229570;JNJ 10229570;UNII-N9IX402L35

    JNJ-10229570 is an antagonist of melanocortin receptor 1 (MC1R) and melanocortin receptor 5 (MC5R), which inhibits sebaceous gland differentiation and the production of sebum-specific lipids.

    价 格:¥电议型 号:T5464产 地:中国大陆

  • T5462Almonertinib阿美替尼;HS-10296

    Hs-10296 is an inhibitor of EGFR activation mutation and tolerant mutation of EGFR T790M, which has only limited activity against wild-type EGFR.

    价 格:¥电议型 号:T5462产 地:中国大陆

  • T5444CLP290CLP-290

    CLP290 is an activator of the neuron-specific K+-Cl cotransporter KCC2 and displays potential for the treatment of a wide range of neurological and psychiatric indications.

    价 格:¥电议型 号:T5444产 地:中国大陆

  • T5427GSK1940029SCD inhibitor 1

    GSK1940029 is a stearoyl-coa desaturase (SCD) inhibitor.

    价 格:¥电议型 号:T5427产 地:中国大陆

  • T5418BAY-293

    BAY-293 is a potent, cell-active SOS1 inhibitor that disrupts the KRAS-SOS1 interaction (IC50: 21 nM).

    价 格:¥电议型 号:T5418产 地:中国大陆

  • T5413ML216CID-49852229

    ML-216 is a small molecule inhibitor of BLM helicase (IC50: 1.8 μM). It showed 28-fold selective against the related helicases RECQ1, RECQ5, and E. coli UvrD (IC50s > 50 μM).

    价 格:¥电议型 号:T5413产 地:中国大陆

  • T5409AZD3229

    AZD3229 is a potent pan-KIT mutant inhibitor for the treatment of gastrointestinal stromal tumors. It demonstrates potent single-digit nM growth inhibition across a broad cell panel.

    价 格:¥电议型 号:T5409产 地:中国大陆

  • T5401GSK2983559 active metaboliteRIPK2 inhibitor 1;RIPK2-IN-1;GSK2983559

    GSK 2983559 (RIP2 kinase inhibitor 1) is a potent, selective receptor-interacting protein-2 (RIP2) kinase inhibitor.

    价 格:¥电议型 号:T5401产 地:中国大陆

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