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T26804Biclotymol;双氯麝酚Biclotymol
Biclotymol is used in the study about infectious oropharyngeal diseases.
价 格:¥电议型 号:T26804产 地:中国大陆
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T26803Bibw 22;化合物 T26803Bibw22|||Bibw-22;Bibw22|||Bibw-22
Bibw 22 is a bifunctional modulator of P-glycoprotein and nucleoside transport.
价 格:¥电议型 号:T26803产 地:中国大陆
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T26802BIBS-222;化合物 T26802BIBS 222;BIBS 222
BIBS-222, a nonpeptide angiotensin II (Ang II) receptor antagonist, appears to be an effective antihypertensive in the model of the renal hypertensive rat.
价 格:¥电议型 号:T26802产 地:中国大陆
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T26801BIBP3226;化合物 T26801BIBP 3226|||BIBP-3226;BIBP 3226|||BIBP-3226
BIBP3226 is a potent and selective antagonist for the Neuropeptide Y receptor Y1 and the neuropeptide FF receptor.
价 格:¥电议型 号:T26801产 地:中国大陆
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T26800BIBO3304;化合物 T26800BIBO-3304|||BIBO 3304;BIBO-3304|||BIBO 3304
BIBO3304 is a selective NPY Y1 receptor antagonist (IC50 values are 0.38 and 0.72 nM at human and rat receptors respectively). BIBO3304 inhibits NPY- and fasting-induced feeding in vivo following central administration.
价 格:¥电议型 号:T26800产 地:中国大陆
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T2680NVP-BVU972;化合物NVP-BVU972NVP-BVU972
NVP-BVU972 is a selective and potent Met inhibitor with IC50 of 14 nM.
价 格:¥电议型 号:T2680产 地:中国大陆
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T26680ATL-801;化合物 T26680ATL-801
ATL-801 is anselective antagonist of A2B receptor with herapeutic activity for colitis.
价 格:¥电议型 号:T26680产 地:中国大陆
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T2666Taladegib;化合物TaladegibLY2940680;LY2940680
Taladegib (LY2940680) is an orally bioavailable small molecule antagonist of the Hedgehog (Hh)-ligand cell surface receptor smoothened (Smo) with potential antineoplastic activity.
价 格:¥电议型 号:T2666产 地:中国大陆
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T2595Lumacaftor;鲁玛卡托VX-809|||VRT 826809;鲁玛卡托|||VX-809|||VRT 826809
Lumacaftor (VRT 826809) is a CFTR modulator that corrects the folding and trafficking of CFTR protein. It enhances F508del-CFTR protein maturation in FRT cells (EC50: 100 nM).
价 格:¥电议型 号:T2595产 地:中国大陆
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T25680Leucinostatin D;化合物 T25680Leucinostatin-D;Leucinostatin-D
Leucinostatin D is a novel peptide antibiotic isolated from Paecilomyces marquandii.
价 格:¥电议型 号:T25680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
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T24680PSB-1491;化合物PSB-1491PSB-1491
PSB-1491 is a selective and competitive monoamine oxidase B inhibitor with IC50 of 0.386 nM, >25000-fold selective versus MAO-A.
价 格:¥电议型 号:T24680产 地:中国大陆
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T24623PF-06807656;化合物 T24623PF 06807656;PF 06807656
PF-06807656 is insensitive to the introduction of the N171D mutation in the ROMK conduction pore that greatly diminishes the activity of other small-molecule inhibitors. PF-06807656 is an effective ROMK inhibitor (Tl+ flux IC50 = 160 nM).
价 格:¥电议型 号:T24623产 地:中国大陆
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T24328L 680833;化合物 T24328L680,833|||L680833|||L-680,833|||L 680,833|||L-680833;L680,833|||L680833|||L-680,
L 680833 is an orally active monocyclic beta-lactam human polymorphonuclear leukocyte elastase inhibitor.
价 格:¥电议型 号:T24328产 地:中国大陆
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T23680AHR-14310C;化合物 T23680AHR-14310C
AHR-14310C is a long-acting and nonsedating H1-antihistamine.
价 格:¥电议型 号:T23680产 地:中国大陆
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T22893L-168049;化合物L-168049L-168,049;L-168,049
L-168049 is a selective and non-competitive antagonist of human glucagon receptor with IC50s of 3.7 nM, 63 nM, and 60 nM for human, murine, and canine, respectively.
价 格:¥电议型 号:T22893产 地:中国大陆
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T22680CP-100356 hydrochloride;CP-100356 盐酸盐CP-100356 HCl|||CP 100356 hydrochloride;CP-100356 HCl|||CP 1003
CP-100356 hydrochloride is an orally active and low micromolar dual inhibitor of MDR1 (P-gp) and BCRP, a nucleotide-derived substrate analogue with inhibitory effects on MDR1-mediated Calcein-AM transporter and BCRP-mediated Prazosin transporter.CP-100356 Inhibits OATP1B1, induces stomatal opening in the dark.
价 格:¥电议型 号:T22680产 地:中国大陆
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T22553Adaphostin;化合物Adaphostin1-Adamantyl 4-((2,5-Dihydroxybenzyl)Amino)Benzoate|||NSC 680410;1-Adamantyl
Adaphostin (NSC-680410) is a p210Bcr/Abl tyrosine kinase inhibitor with IC50 of 14 μM.
价 格:¥电议型 号:T22553产 地:中国大陆
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T22251680C91;化合物680C91680C91
680C91 is a potent and selective inhibitor of TDO, and its Ki is 51 nM.
价 格:¥电议型 号:T22251产 地:中国大陆
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T21680A 68930 hydrochloride;化合物 T21680A 68930 hydrochloride
A68930 hydrochloride is a dopamine D1 receptor agonist which can be used for the research of bronchiectasis [1].
价 格:¥电议型 号:T21680产 地:中国大陆