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T8972FIT-039Cytomegalovirus,HSV-1,Herpes simplex virus,transcription,Inhibitor,DNA,CDK,Cyclin dependent k
FIT-039 is a selective and ATP-competitive, orally active inhibitor of CDK9( IC50 : 5.8 μM;CDK9/cyclin T1). FIT-039 inhibits replication of HSV-1 (IC50 of 0.69 μM), HSV-2, human adenovirus, and human CMV. FIT-039 is a promising antiviral agent for inhibiting drug-resistant HSVs and other DNA viruses.
价 格:¥电议型 号:T8972产 地:中国大陆
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T8997WWL229WWL 229,WWL-229,Inhibitor,inhibit,WWL229
WWL229 is a selective inhibitor of Ces3 . WWL229 acts by inhibiting recombinant Ces3 but not Ces1f, ABHD6 or other tested serine hydrolases, and recapitulating the effects of WWL113 in adipocytes.
价 格:¥电议型 号:T8997产 地:中国大陆
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T9718Ethoxylated hydrogenated castor oilInhibitor,PEG,Ethoxylated hydrogenated castor oil,Macrogolglycero
Ethoxylated hydrogenated castor oil is a combination of synthetic polyethylene glycol (PEG) with natural castor oil. Ethoxylated hydrogenated castor oil can be used to emulsify and solubilize oil-in-water (o/w) emulsions.
价 格:¥电议型 号:T9718产 地:中国大陆
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T8697ZAP-180013Inhibitor,autoimmune,ZAP-70,tyrosine,T-cell,ZAP 180013,ZAP180013,Tyrosinase,ZAP-180013,ant
ZAP-180013 is an inhibitor of zeta-chain-associated protein kinase 70 (ZAP70,IC50 : 1.8 μM).
价 格:¥电议型 号:T8697产 地:中国大陆
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T8297Gomisin NGomisin N,Inhibitor,Apoptosis,inhibit
Gomisin N, isolated from Schisandra chinensis, produces beneficial sedative and hypnotic bioactivity. It has the potential for use in the treatment of allergy and inhibits proliferation and induces apoptosis in cancer.
价 格:¥电议型 号:T8297产 地:中国大陆
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T7502PF 05089771 tosylatePF 05089771 tosylate,TTX-R,pain,Na channels,PF-05089771,neuropathy,diabetic,Sodi
PF-05089771 is a voltage-gated sodium channel 1.7 (Nav1.7) blocker (IC50: 11, 16, 33, and 20 nM for 5N11S, 5A11L, 5A11S, and 5A11L Nav1.7 splice variants, respectively). It is selective for Nav1.7 over Nav1.1-1.6 and 1.8 channels (IC50: 0.11-25 μM), L-type calcium, and KvLQT and hERG potassium channels (IC50: ≥10 μM), as well as human and cynomolgus monkey TRPV1 receptors (IC50: 10/20 μM). PF-05089771 is also 1, 000-fold selective for half-inactivated over resting Nav1.7 channels, and mutation o
价 格:¥电议型 号:T7502产 地:中国大陆
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T97803,4,5-TrimethoxyphenyL3,4,5 TrimethoxyphenyL,3,4,5TrimethoxyphenyL
3,4,5-TrimethoxyphenyL, an intermediate metabolite of mescaline, is oxidized from the oxidation of 3,4,5-Trimethoxyphenylacetaldehyde by mouse hepatic microsomes. The reaction was NADPH-dependent, and inhibited by SKF 525-A, metyrapone and disulfiram.
价 格:¥电议型 号:T9780产 地:中国大陆
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TP1291Epithalon TFA (307297-39-8 free base)Epithalon TFA (307297 39 8 free base),Epithalon TFA (307297398
Epitalon TFA is an anti-aging agent and telomerase activator.
价 格:¥电议型 号:TP1291产 地:中国大陆
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T9022AZD9977AZD9977,Inhibitor,T2DM,AZD-9977,Mineralocorticoid Receptor,Chronic Kidney Disease,?type 2 dia
AZD 9977 is a novel, selective modulator of mineralocorticoid receptor .
价 格:¥电议型 号:T9022产 地:中国大陆
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T6597Mosapride CitrateTAK-370,5-hydroxytryptamine Receptor,AS4370,TAK370,AS 4370,Inhibitor,Mosapride Citr
Mosapride Citrate, a gastroprokinetic agent, utilizes as a selective 5HT4 agonist.
价 格:¥电议型 号:T6597产 地:中国大陆
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T6973RS-127445inhibit,Inhibitor,Serotonin Receptor,RS-127445,5-HT Receptor,RS 127445,RS127445,5-hydroxytr
RS-127445 is a selective 5-HT2B receptor antagonist with pKi of 9.5 and pIC50 of 10.4, exhibits >1000-fold selectivity against other 5-HT receptors.
价 格:¥电议型 号:T6973产 地:中国大陆
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T9706BTK inhibitor 17BTK inhibitor17,oral,BTK inhibitor 17,Btk,rheumatoid,Inhibitor,inhibit,Cys481,Bruton
BTK inhibitor 17 is a potent irreversible BTK inhibitor (IC50 = 2.1 nM). BTK inhibitor 17 can be used in rheumatoid arthritis studies.
价 格:¥电议型 号:T9706产 地:中国大陆
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T9528ARN19702ARN19702,ARN-19702
ARN19702 is a selective, orally active, reversible, and brain-penetrant N-acylethanolamine acid amidase (NAAA) inhibitor with an IC 50 of 230 nM for human NAAA. ARN19702 exhibits a broad analgesic profile [1] [2].
价 格:¥电议型 号:T9528产 地:中国大陆
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T22947LY266097 hydrochlorideLY-266097 hydrochloride,LY266097 hydrochloride
LY266097 hydrochloride is an antagonist of 5-HT2 with pKis of 7.7, 9.8, and 7.6 for human 5-HT2A, 5-HT2B, and 5-HT2C and can be used in studies about depression.
价 格:¥电议型 号:T22947产 地:中国大陆
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T7497L1C3a 70-77 acetateC3a 7077 acetate,C-3a 70-77 acetate,C3a 70 77 acetate
C3a 70-77 acetate is the octapeptide acetate corresponding to the COOH terminus of C3a, exhibits the specificity and 1 to 2% biologic activities of C3a.
价 格:¥电议型 号:T7497L1产 地:中国大陆
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TP1197SincalidePI3K/Akt,cardiovascular hormone,Inhibitor,SQ 19844,PI3K,Akt,Protein kinase B,Apoptosis,SQ-1
Sincalide (INN) is a cholecystokinetic drug administered by injection to aid in diagnosing disorders of the gallbladder and pancreas. It is the 8-amino acid C-terminal fragment of cholecystokinin, and also known as CCK-8.
价 格:¥电议型 号:TP1197产 地:中国大陆
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T9786Lu AF27139Inhibitor,P2XRs,oral,P2X7,rodent-active,Lu AF 27139,CNS-penetrant,CNS,Lu AF27139,Lu AF-271
Lu AF27139 is an effective and selective antagonist of P2X7 receptor (IC50s of 12 and 2.4 nM for human and rat, Kis of 22, 54, and 13 nM for mouse, human, and rat, respectively). Lu AF27139 can be used in CNS diseases studies.
价 格:¥电议型 号:T9786产 地:中国大陆
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T97465-methoxy-α-Ethyltryptamine5 methoxy α Ethyltryptamine,5methoxyαEthyltryptamine
5-Methoxy-alpha-ethyltryptamine is a psychoactive substance that can cause various effects. It belongs to the tryptamine chemical class and can be used for various psychoactive and stimulant effects.
价 格:¥电议型 号:T9746产 地:中国大陆
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TN1997Notoginsenoside FP2Notoginsenoside FP2,Notoginsenoside FP-2
Notoginsenoside FP2 is a natural product isolated from the fruit pedicels of Panax notoginseng and can be used in studies about the treatment of cardiovascular diseases.
价 格:¥电议型 号:TN1997产 地:中国大陆
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T6697TCIDhydrolase,C-terminal,Neuronal,Deubiquitinase,transporter,ubiquitination,DUBs,inhibit,TCID,glycin
TCID(IC50=0.6 μM) is a DUB inhibitor of ubiquitin C-terminal hydrolase L3. It has the 125-fold selectivity to L1.
价 格:¥电议型 号:T6697产 地:中国大陆