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T71169XMD-12;化合物 XMD-12XMD-12
XMD-12, also known as DUN57447, Aurora inhibitor (compound 1) or Aurora-IN-1, is an Auroro inhibitor, which targets Aurora A/B/C. (5.6/18.4/24.6 nM).
价 格:¥电议型 号:T71169产 地:中国大陆
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T71168Epetraborole R-Mandelate;化合物 Epetraborole R-MandelateEpetraborole R-Mandelate
Epetraborole R-Mandelate is a potent and selective leucyl-tRNA synthetase inhibitor.
价 格:¥电议型 号:T71168产 地:中国大陆
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T71166PF-05150122;化合物 PF-05150122PF-05150122
PF-05150122 is a novel potent and selective human Nav1.7 blocker.
价 格:¥电议型 号:T71166产 地:中国大陆
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T71165MK-1421;化合物 MK-1421MK-1421
MK-1421 is a potent and selective sstr3 antagonist.
价 格:¥电议型 号:T71165产 地:中国大陆
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T71164CXN37378;化合物 CXN37378CXN37378
CXN37378, also known as NAP, is a potent and selective antagonist for the μ-opioid receptor (MOR). This product has no formal name at the moment. For the convenience of communication, a temporary code name was therefore proposed according to MedKoo Chemical Nomenclature (see web page: https://www.medkoo.com/page/naming).
价 格:¥电议型 号:T71164产 地:中国大陆
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T71163Pimasertib HCl;化合物 Pimasertib HClPimasertib HCl
Pimasertib HCl is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity. Pimasertib selectively binds to and inhibits the activity of MEK1/2, preventing the activation of MEK1/2-dependent effector proteins and transcription factors, which may result in the inhibition of growth factor-mediated cell signaling and tumor cell proliferation. MEK1/2 (MAP2K1/K2) are dual-specificity threonine/tyrosine kinases that play key roles in the activati
价 格:¥电议型 号:T71163产 地:中国大陆
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T71162MDL-73811;化合物 MDL-73811MDL-73811
MDL-73811 is a potent AdoMetDC (S-adenosylmethionine decarboxylease) inhibitor and anti-trypanosomal compound that cures Brucella infections in mice. However despite the good activity of MDL 73811, rapid plasma clearance and poor brain penetration hindered its further development.
价 格:¥电议型 号:T71162产 地:中国大陆
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T71161Thiorphan disulfide;化合物 Thiorphan disulfideThiorphan disulfide
Thiorphan disulfide is an impurity of Racecadotril -- an antidiarrheal and enkephalinase inhibitor that reduces the amount of water and electrolytes absorbed into the intestine.
价 格:¥电议型 号:T71161产 地:中国大陆
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T71160Levomepromazine HCl;化合物 Levomepromazine HClLevomepromazine HCl
Levomepromazine HCl is a phenothiazine with pharmacological activity similar to that of both CHLORPROMAZINE and PROMETHAZINE. It has the histamine-antagonist properties of the antihistamines together with CENTRAL NERVOUS SYSTEM effects resembling those of chlorpromazine.
价 格:¥电议型 号:T71160产 地:中国大陆
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T7116Sodium gualenate;磺酸钠Guaiazulenesulfonate sodium;Guaiazulenesulfonate sodium|||磺酸钠
Sodium gualenate (Guaiazulenesulfonate sodium) (Guaiazulenesulfonate sodium), a hydrophilic derivative of guaiazulene (GA), is an unstable compound. It has anti-inflammatory and wound-healing effects.
价 格:¥电议型 号:T7116产 地:中国大陆
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T71116MPT0B098;化合物 MPT0B098MPT0B098
MPT0B098 is a potent microtubule inhibitor through binding to the colchicine-binding site of tubulin. MPT0B098 is active against the growth of various human cancer cells, including chemoresistant cells with IC50 values ranging from 70 to 150 nmol/L. MPT0B098 arrests cells in the G2?–M phase and subsequently induces cell apoptosis. In addition, MPT0B098 effectively suppresses VEGF-induced cell migration and capillary-like tube formation of HUVECs. Distinguished from other microtubule inhibitors,
价 格:¥电议型 号:T71116产 地:中国大陆
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T6S2116Ginkgolic acid C17:1银杏酸 C17:1银杏酸 C17:1|||银杏酸C17:1
1. Ginkgolic acid C17:1 can significantly inhibit enterohemorrhagic Escherichia coli O157:H7(EHEC) biofilm formation on the surfaces of polystyrene and glass, and on nylon membranes.
价 格:¥电议型 号:T6S2116产 地:中国大陆
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T69116Agroclavine;化合物 AgroclavineAgroclavine
Agroclavine is a clavine type of ergot alkaloid with D1 dopamine and a-adrenoceptor agonistic properties.
价 格:¥电议型 号:T69116产 地:中国大陆
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T68900SU11606;化合物 SU11606SU11606
SU11606 is a potent c-MET inhibitor with potential anticancer activity.
价 格:¥电议型 号:T68900产 地:中国大陆
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T68116L(Rac)-Norcisapride;化合物(Rac)-Norcisaprideide(Rac)-Norcisapride
Norcisapride is a 5-hydroxytryptamine receptor 3 (5-HT3) and (5-hydroxytryptamine receptor 4 (5-HT4) dual agonist used for the treatment of gastrointestinal disorders, orofacial disorders, and otorhinolaryngologic disorders.
价 格:¥电议型 号:T68116L产 地:中国大陆
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T67799Goxalapladib;戈沙拉地GSK 677116;GSK 677116
Goxalapladib(GSK 677116) is a small molecule compound that can be used to treat cardiovascular risks associated with atherosclerosis.
价 格:¥电议型 号:T67799产 地:中国大陆
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T671162,5-Bis(trifluoromethyl)aniline;化合物 2,5-Bis(trifluoromethyl)aniline2,5-Bis(trifluoromethyl)aniline
2,5-Bis(trifluoromethyl)aniline is a useful organic compound for research related to life sciences. The catalog number is T67116 and the CAS number is 328-93-8.
价 格:¥电议型 号:T67116产 地:中国大陆
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T66116Boc-N-Me-Tyr(Bzl)-OH;化合物 Boc-N-Me-Tyr(Bzl)-OHBoc-N-Me-Tyr(Bzl)-OH
Boc-N-Me-Tyr(Bzl)-OH is a useful organic compound for research related to life sciences. The catalog number is T66116 and the CAS number is 64263-81-6.
价 格:¥电议型 号:T66116产 地:中国大陆
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T65116Boc-4-phenyl-Phe-OH;化合物 Boc-4-phenyl-Phe-OHBoc-4-phenyl-Phe-OH
Boc-4-phenyl-Phe-OH is a useful organic compound for research related to life sciences. The catalog number is T65116 and the CAS number is 147923-08-8.
价 格:¥电议型 号:T65116产 地:中国大陆
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T6458CYC-116噻氯匹定噻氯匹定
CYC116 is a potent inhibitor of Aurora A/B with Ki of 8.0 nM/9.2 nM, is less potent to VEGFR2 (Ki of 44 nM), with 50-fold greater potency than CDKs, not active against PKA, Akt/PKB, PKC, no effect on GSK-3α/β, CK2, Plk1 and SAPK2A. Phase 1.
价 格:¥电议型 号:T6458产 地:中国大陆