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T21014Thonzylamine hydrochloride
Thonzylamine hydrochloride is an anticholinergic and antihistamine used as an antipruritic.
价 格:¥电议型 号:T21014产 地:中国大陆
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T9021Ro0711401Ro0711401,Metabotropic glutamate receptors,mGluR,oral,PAM,Inhibitor,mGlu1,inhibit
Ro0711401 is an agonist of mGlu1 receptor.
价 格:¥电议型 号:T9021产 地:中国大陆
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TP1381LHAEGT TFA(852155-81-8 free base)HAEGT TFA(852155 81 8 free base),HAEGT TFA(852155818 free base)
HAEGT TFA is the first N-terminal 1-5 residues of GLP-1 peptide.
价 格:¥电议型 号:TP1381L产 地:中国大陆
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T9214ELOVL6-IN-1ELOVL6IN1,noncompetitive,orally,palmitoyl-CoA,potent,malonyl-CoA,ELOVL-6-IN-1,Inhibitor,s
ELOVL6-IN-1 is a potent, orally active and selective ELOVL6 inhibitor. ELOVL6-IN-1 dose-dependently inhibits mouse ELOVL6 activities, with an IC50 value of 0.350 μM. ELOVL6-IN-1 inhibits ELOVL6 in a noncompetitive manner for malonyl-CoA (Ki=994 nM) and palmitoyl-CoA[1].
价 格:¥电议型 号:T9214产 地:中国大陆
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TP2111LTAT-GluA2 3Y acetate(1404188-93-7 free base)TAT-GluA-2 3Y acetate(1404188-93-7 free base),TATGluA2 3
TAT-GluA2 3Y acetate is an inhibitor of AMPA receptor endocytosis. Induces increased hind paw withdrawal latencies following thermal and mechanical stimuli in rats. Also exhibits antinociceptive effects in a rat model of neuropathic pain. Rescues pentobarbital-induced memory retrieval deficits in a rat model of learning and memory.
价 格:¥电议型 号:TP2111L产 地:中国大陆
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TN2154Rhein 8-GlucosideRhein 8Glucoside,Inhibitor,Rhein 8-Glucoside,Rhein 8 Glucoside,inhibit
Rhein-8-glucoside has low laxative activity.
价 格:¥电议型 号:TN2154产 地:中国大陆
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T11121DuoperoneDuoperone
Duoperone is a neuroleptic agent. Duoperone shows antiemetic activity in animal models.
价 格:¥电议型 号:T11121产 地:中国大陆
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TN7121d-Epigalbacin
d-Epigalbacin is a naturally occurring lignin. d-Epigalbacin is a potent, selective JNKs inhibitor, with IC50s of 1.7 μM, 2.9 μM and 1.74 μM for JNK1, JNK2 and JNK3, respectively.
价 格:¥电议型 号:TN7121产 地:中国大陆
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T4341BetrixabanBetrixaban,PRT-054021,Factor Xa,inhibit,Fxa,PRT 054021,Inhibitor
Betrixaban is a non-vitamin K oral anticoagulant whose action is driven by the competitive and reversible inhibition of the factor Xa [1]. It was selected among all lead compounds due to its low hERG channel affinity while sustaining its factor Xa inhibition capacity [3]. Betrixaban, now developed by Portola Pharmaceuticals Inc., is prescribed as a venous thromboembolism (VTE) prophylactic for adult patients with moderate to severe restricted motility or with other risks for VTE [2]. VTE can be
价 格:¥电议型 号:T4341产 地:中国大陆
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T21142Bupirimate
Bupirimate, an active ingredient in plant protection products, is commonly used as a systemic fungicide and finds applications in controlling powdery mildew in roses, apple plantations. It belongs to the family of pyrimidines.
价 格:¥电议型 号:T21142产 地:中国大陆
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TP1459LGly-Arg-Gly-Asp-Ser acetate(96426-21-0 free base)GlyArgGlyAspSer acetate(96426210 free base),Gly Arg
Gly-Arg-Gly-Asp-Ser (GRGDS) acetate is a cell binding protein domain derived from the cell-binding region of fibronectin.
价 格:¥电议型 号:TP1459L产 地:中国大陆
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TN2125Quercetin 3-O-β-D-(6’’-p-coumaroyl)glucopyranosyl(1→2)-α-L-rhamnopyranosideQuercetin 3OβD(6’’pcoumar
Quercetin 3-O-beta-(6´´-p-coumaroyl)glucopyranosyl(1->2)-alpha-L-rhamnopyranoside is a natural product
价 格:¥电议型 号:TN2125产 地:中国大陆
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T7221SatraplatinBMY 45594,DNA Alkylator/Crosslinker,BMS-182751,Satraplatin,BMY-45594,JM 216,inhibit,Inhib
Satraplatin is an orally available antineoplastic platinum(IV) complex.Satraplatin has a favorable toxicity profile and appears to have clinical activity against a variety of malignancies.
价 格:¥电议型 号:T7221产 地:中国大陆
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T9521CHR-6494 TFACHR-6494,inhibit,apoptosis,Haspin Kinase,NRAS mutant melanoma cells,CHR 6494,mitotic cat
CHR-6494 TFA is a potent haspin inhibitor, with an?IC50?of 2 nM. It inhibits histone H3T3 phosphorylation. CHR-6494 TFA induces the?apoptosis?of cancer cells, including melanoma and breast cancer. CHR-6494 TFA can be used in the research of cancer
价 格:¥电议型 号:T9521产 地:中国大陆
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T6527GW842166XGW842166X,inhibit,Cannabinoid Receptor,GW-842166X,Inhibitor
GW842166X is a potent and highly selective agonist of cannabinoid receptor CB2 receptor with EC50 of 63 nM, shows no significant activity at CB1 receptor. Phase 2.
价 格:¥电议型 号:T6527产 地:中国大陆
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T8221Insulin (human)Insulin Receptor,Inhibitor,Insulin (human),inhibit
INSULIN is a polypeptide hormone that regulates the level of glucose.
价 格:¥电议型 号:T8221产 地:中国大陆
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T8974ML-211MAGL,ML 211,inhibit,Phospholipase,Monoacylglycerol lipase,ML-211,Inhibitor,ML211
ML-211 is a carbamate-based dual inhibitor of LYPLA1 (IC50 = 17 nM) and the related LYPLA2 (IC50 = 30 nM)
价 格:¥电议型 号:T8974产 地:中国大陆
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T67755WAY-312157WAY312157
WAY-312157 is a potent Protein kinase G inhibitor, IC50= 0.9 uM.
价 格:¥电议型 号:T67755产 地:中国大陆
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T9213G140Inhibitor,cGAS,anti-inflammatory,G 140,Cyclic GMP-AMP Synthase,G140,synthase,G-140,GMP-AMP,cycli
G140 is a potent and selective inhibitor of cyclic GMP-AMP synthase (cGAS).
价 格:¥电议型 号:T9213产 地:中国大陆
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T21747VU0483605Inhibitor,inhibit,VU0483605,Metabotropic glutamate receptors,allosteric modulator,brain pen
VU0483605 is an effective and selective positive allosteric modulator of mGluR1 with EC50s of 390 and 356 nM for human and rat, respectively.
价 格:¥电议型 号:T21747产 地:中国大陆