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T26841BMS 182874;化合物BMS 182874BMS182874|||BMS-182874;BMS182874|||BMS-182874
BMS 182874 is an orally effective and highly selective endothelin receptor ETA antagonist with an IC50 value of 0.150 μM for ETA and a Ki value of 0.055 μM for ETA.BMS 182874 is able to reduce arterial pressure in a rat hypertension model induced by Deoxycorticosterone acetate. BMS 182874 was able to reduce Deoxycorticosterone-induced arterial pressure in a rat model of hypertension and can be used to study cardiovascular disease.
价 格:¥电议型 号:T26841产 地:中国大陆
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T26840BMH-7;化合物 T26840BMH7;BMH7
BMH-7 is a p53 activator with potent antitumor activity.
价 格:¥电议型 号:T26840产 地:中国大陆
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T26839BM 21.1298;化合物 T26839BM21.1298|||BM-21.1298;BM21.1298|||BM-21.1298
BM 21.1298 is a inhibition of HIV-1 reverse transcriptase.
价 格:¥电议型 号:T26839产 地:中国大陆
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T2679BMS-265246;化合物BMS-265246BMS265246;BMS265246
BMS-265246 is a potent and selective CDK1/2 inhibitor.
价 格:¥电议型 号:T2679产 地:中国大陆
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T26641Apadenoson;化合物 T26641ATL 146e|||BMS 068645|||ATL146e|||BMS-068645|||ATL-146e|||BMS068645;ATL 146e|||
Apadenoson is a potent Adenosine A2 receptor agonist with inhibitory effects on Adenosine A3 receptors with an IC of 45 nM. Apadenoson has anti-inflammatory activity and can be used to study neurological diseases.
价 格:¥电议型 号:T26641产 地:中国大陆
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T26637Antipain dihydrochloride抗痛素盐酸盐Antipain 2HCl|||BDBM-32804|||BDBM 32804, Antipain|||BDBM32804
Antipain dihydrochloride (Antipain 2HCl) is a protease inhibitor derived from Actinomycetes that exhibits analgesic activity and inhibits X-ray-induced chromosomal aberrations in human lymphocytes.
价 格:¥电议型 号:T26637产 地:中国大陆
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T26361LBrasofensine Maleate;化合物 T26361LNS-2214|||NS 2214|||BMS-204756-07|||NS2214;NS-2214|||NS 2214|||BMS-2
Brasofensine Maleate inhibits the monoamine re-uptake.
价 格:¥电议型 号:T26361L产 地:中国大陆
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T26361Brasofensine sulfate;化合物 T26361NS 2214|||BMS 204756|||NS2214|||NS-2214|||BMS-204756;NS 2214|||BMS 20
Brasofensine sulfate is a dopamine reuptake inhibitor.
价 格:¥电议型 号:T26361产 地:中国大陆
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T26326VU0285655-1;消旋-7-氧代普拉克索VU-0285655|||VU0285655|||BML 280|||VU 0285655|||BML280|||BML-280;VU-0285655||
VU0285655-1(BML-280) is a potent and selective phospholipase D2 (PLD2) inhibitor that inhibits the proliferation of PLD2-deficient cells.VU0285655-1 has an inhibitory effect on high glucose-induced caspase-3 cleavage and reduction of cell viability.VU0285655-1 is used in the study of diabetic retinopathy.
价 格:¥电议型 号:T26326产 地:中国大陆
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T2610LBMS-599626 2HCL(714971-09-2 Free base);化合物 BMS-599626 2HCL(714971-09-2 Free base)BMS 599626 dihydroc
BMS-599626 2HCL (AC480 2HCl) is a BMS-599626 derivative. BMS-599626 is an orally available and selective dual inhibitor of HER1 and HER2 with IC50s of 20 and 30 nM, respectively. BMS-599626 inhibits tumor cell proliferation and has the potential to increase tumor BMS-599626 inhibits tumor cell proliferation and has the potential to increase tumor response to radiotherapy.
价 格:¥电议型 号:T2610L产 地:中国大陆
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T2610BMS-599626;化合物BMS 599626AC480;AC480
BMS-599626 (AC480) has been used in trials studying the treatment of Cancer, Metastases, and HER2 or EGFR Expressing Advanced Solid Malignancies.
价 格:¥电议型 号:T2610产 地:中国大陆
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T2586Cabozantinib卡博替尼卡博替尼|||XL184|||BMS-907351
Cabozantinib (XL184) is a multi-targeted tyrosine kinase receptor inhibitor that inhibits VEGFR2, c-Met, Kit, Axl, and Flt3 (IC50=0.035/1.3/4.6/7/11.3 nM). Cabozantinib exhibits both antitumor and antiangiogenic activity.
价 格:¥电议型 号:T2586产 地:中国大陆
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T2576Brivanib (alaninate);丙氨酸布立尼布BMS-582664|||Brivanib Alaninate;丙氨酸布立尼布|||BMS-582664|||Brivanib Alaninat
Brivanib Alaninate (BMS-582664) is the alaninate salt of a vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with potential antineoplastic activity. Brivanib strongly binds to and inhibits VEGFR2, a tyrosine kinase receptor expressed almost exclusively on vascular endothelial cells; inhibition of VEGFR2 may result in inhibition of tumor angiogenesis, inhibition of tumor cell growth, and tumor regression.
价 格:¥电议型 号:T2576产 地:中国大陆
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T2545Lomitapide Mesylate甲磺酸洛美他派甲磺酸洛美他派|||BMS-201038 mesylate|||AEGR-733 mesylate
Lomitapide Mesylate (BMS-201038 mesylate) is a methanesulfonic acid form of lomitapide, a small molecule inhibitor of microsomal triglyceride transfer protein.
价 格:¥电议型 号:T2545产 地:中国大陆
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T25166BMS-663749 lysine;化合物 T25166BMS-663749 lysine salt|||BMS663749 lysine|||BMS 663749 lysine;BMS-663749
BMS-663749 lysine is used as a phosphonooxymethyl prodrug 4 for HIV-1 attachment inhibitor.
价 格:¥电议型 号:T25166产 地:中国大陆
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T25165LBMS-189664 HCl;化合物 T25165LBMS 189664 HCl|||BMS189664 HCl|||BMS-189664 hydrochloride;BMS 189664 HCl||
BMS-189664 HCl is a selective and orally active thrombin active site inhibitor.
价 格:¥电议型 号:T25165L产 地:中国大陆
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T25165BMS-189664;化合物 T25165BMS-189664
BMS-189664 is an inhibitor of thrombin.
价 格:¥电议型 号:T25165产 地:中国大陆
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T25164BMS 180742;化合物 T25164BMS-180742|||BMS180742;BMS-180742|||BMS180742
BMS 180742 is an exosite inhibitor of thrombin.
价 格:¥电议型 号:T25164产 地:中国大陆
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T2516Amuvatinib;化合物AmuvatinibMP470|||HPK 56;MP470|||HPK 56
Amuvatinib (MP470) is an orally bioavailable synthetic carbothioamide with potential antineoplastic activity.
价 格:¥电议型 号:T2516产 地:中国大陆
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T2509Tozasertib;化合物TozasertibMK-0457|||VX 680;MK-0457|||VX 680
Tozasertib (MK-0457) is a pan-Aurora kinase inhibitor (Kis: 0.6/18/4.6 nM for Aurora A/Aurora B/Aurora C). It shows selectivity against more than 190 different kinases.
价 格:¥电议型 号:T2509产 地:中国大陆