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T16107ML230;化合物 T16107CID44640177|||SID 88095709;CID44640177|||SID 88095709
ML230 is a selective ATP-binding cassette (ABC) transporter ABCG2 inhibitor. It 36-fold selective for ABCG2 over ABCB1 (EC50s: 0.13 μM and 4.65 μM, respectively).
价 格:¥电议型 号:T16107产 地:中国大陆
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T16090LMK-0773 FA;MK-0773 甲酸盐MK-0773 FA (606101-58-0 Free base);MK-0773 FA (606101-58-0 Free base)
MK-0773 FA (MK-0773 FA (606101-58-0 Free base)) is a selective androgen receptor modulator with an IC50 value of 6.6 nM for AR, which can be used for the prevention and treatment of cancer-related muscle wasting.
价 格:¥电议型 号:T16090L产 地:中国大陆
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T16090MK-0773;化合物 MK-0773PF-05314882;PF-05314882
MK-0773 (PF-05314882) is a selective androgen receptor modulator that binds to AR (IC50: 6.6 nM) for the study of diseases caused by endocrine abnormalities.
价 格:¥电议型 号:T16090产 地:中国大陆
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T1606Fasudil;法舒地尔HA-1077|||AT877;HA-1077|||AT877|||法舒地尔
Fasudil (HA-1077) is a potent inhibitor of ROCK1, PKA, PKC, and MLCK.
价 格:¥电议型 号:T1606产 地:中国大陆
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T15977Mal-PEG1-PFP ester;化合物 T15977Mal-PEG1-PFP ester
Mal-PEG1-PFP ester, an alkyl/ether-based PROTAC linker, is utilized in PROTAC synthesis.
价 格:¥电议型 号:T15977产 地:中国大陆
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T15944M77976;化合物M77976M77976
M77976 is a selective ATP-competitive inhibitor of pyruvate dehydrogenase kinase 4 (PDK4) with an inhibitory effect on PDK4, having an IC50 value of 648 μM. It is used for research related to obesity and diabetes.
价 格:¥电议型 号:T15944产 地:中国大陆
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T15819LY377604;化合物 LY377604LY377604
LY377604 is a human β3-adrenergic receptor agonist (EC50: 2.4 nM) and β1/2-adrenergic receptor antagonist for the study of obesity.
价 格:¥电议型 号:T15819产 地:中国大陆
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T15779LP-533401 hydrochloride;LP-533401 盐酸盐LP-533401 hydrochloride
LP-533401 hydrochloride is a peripheral Tph inhibitor that cannot cross the blood-brain barrierthat inhibits 5-hydroxytryptamine synthesis and can be used to study periodontal disease and hepatic steatosis.
价 格:¥电议型 号:T15779产 地:中国大陆
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T15778LP-533401化合物 T15778LP533401|||LP 533401
LP-533401 is an inhibitor of Tryptophan hydroxylase 1. It is used for regulates serotonin production in the gut.
价 格:¥电议型 号:T15778产 地:中国大陆
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T15777Loxoribine;洛索立宾RWJ 21757|||7-Allyl-8-oxoguanosine;RWJ 21757|||7-Allyl-8-oxoguanosine|||洛索立宾
Loxoribine (RWJ 21757) is a guanosine analog. Loxoribine is an orally bioavailable and selective Toll-like receptor (TLR) 7 agonist. It has anti-viral and anti-tumor activities.Loxoribine is a potent new immunostimulant with a relatively broad spectrum of immunobiological activities.
价 格:¥电议型 号:T15777产 地:中国大陆
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T15776Loviride化合物 T15776R 89439
Loviride is a non-nucleoside reverse transcriptase inhibitor (IC50: 0.3 μM). Loviride inhibits HIV-1, HIV-2 and SIV replication in MT-4 cells. It is used for reverse transcriptase from HIV-1.
价 格:¥电议型 号:T15776产 地:中国大陆
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T15775Lotilaner;洛替拉纳Lotilaner
Lotilaner is a parasiticide. It is used as a potent non-competitive antagonist of insects GABACl receptors (IC50 of 23.84 nM for Drosophila melanogaster GABA receptor). It also has no effect on a dog GABAA receptor.
价 格:¥电议型 号:T15775产 地:中国大陆
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T15774Losmiprofen;氯米洛芬Losmiprofen
Losmiprofen is a nonsteroidal compound of antiinflammatory.
价 格:¥电议型 号:T15774产 地:中国大陆
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T15773Lofepramine;洛非帕明Gamanil|||Amplit|||Leo 640|||Lopramine;Gamanil|||洛非帕明|||Amplit|||Leo 640|||Lopramine
Lofepramine (Leo 640) is a potent tricyclic antidepressant that is extensively metabolized to desipramine. It inhibits the serotonin and norepinephrine transporters by inhibiting neurons with Kd values of 70 and 5.4 nM, respectively, with weak antagonism of serotonin, histamine and muscarinic receptors.
价 格:¥电议型 号:T15773产 地:中国大陆
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T15772Lodoxamide tromethamine;洛度沙胺氨丁三醇U-42585E;U-42585E
Lodoxamide tromethamine is a mast cell stabilizer with anti-allergic properties and can be used in studies about the treatment of asthma and allergic conjunctivitis.
价 格:¥电议型 号:T15772产 地:中国大陆
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T15771Lobaplatin;络铂D-19466;D-19466|||络铂
Lobaplatin (D-19466) (D-19466) is a diastereometric mixture of platinum(II) complexe. Lobaplatin (D-19466) is a third-generation platinum anti-neoplastic agent which shows activity for a variety of tumour types and is a promising antitumour chemotherapeutic agent[1][2]. It is a platinum complex with DNA alkylating activity.
价 格:¥电议型 号:T15771产 地:中国大陆
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T15770(Rac)-CP-609754;化合物 T15770LNK754;LNK754
LNK754 is a farnesyltransferase inhibitor. It is used for the treatment of cancer and Alzheimer´s disease.
价 格:¥电议型 号:T15770产 地:中国大陆
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T1577Midodrine hydrochloride;盐酸米多君Pro-Amatine;Pro-Amatine|||盐酸米多君
Midodrine is converted to its active metabolite, desglymidodrine by deglycination reaction. Desglymidodrine selectively binds to and activates alpha-1-adrenergic receptors of the arteriolar and venous vasculature. This causes smooth muscle contraction and leads to an elevation of blood pressure. Desglymidodrine diffuses poorly across the blood-brain barrier and is therefore not associated with effects on the central nervous system. Midodrine hydrochloride (Pro-Amatine) is the hydrochloride salt
价 格:¥电议型 号:T1577产 地:中国大陆
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T1570Telmisartan;替米沙坦BIBR 277;BIBR 277|||替米沙坦
Telmisartan (BIBR 277) is an Angiotensin 2 Receptor Blocker. The mechanism of action of telmisartan is as an Angiotensin 2 Receptor Antagonist.
价 格:¥电议型 号:T1570产 地:中国大陆
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T15688L-771688;化合物L-771688SNAP 6383;SNAP 6383
L-771688 (SNAP 6383) is a novel potent and selective α1A-adrenoceptor antagonist with a Ki value of 0.43±0.02 nM.L-771688 KE is used for the treatment of benign prostatic hyperplasia.
价 格:¥电议型 号:T15688产 地:中国大陆