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T1071LDL-Adrenaline HydrochlorideDL-Adrenaline Hydrochloride
DL-Adrenaline Hydrochloride is the hydrochloride salt of the naturally occurring sympathomimetic amine with vasoconstricting, intraocular pressure-reducing activities.
价 格:¥电议型 号:T1071L产 地:美洲
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T10778CGP 20712 ACGP 20712 A,CGP 20712 mesylate,
CGP 20712 A (CGP 20712 mesylate) is a highly selective antagonist of β1-adrenoceptor (IC50: 0.7 nM). It shows ~10,000-fold selectivity over β2-adrenoceptors.
价 格:¥电议型 号:T10778产 地:美洲
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T11071Dofequidar fumarateDofequidar fumarate,MS-209,
It has been reported that an orally active quinoline compound, dofenacid fumarate (MS-209 fumarate), can overcome MDR by inhibiting ABCB1/P-gp, ABCC1/MDR-related protein 1 or both. IC50 value: Target: In vitro P-gp: 3 microM MS-209 effectively overcomes d
价 格:¥电议型 号:T11071产 地:美洲
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T11581HSR6071HSR6071
HSR6071 is an antiallergic agent with potential for the treatment of asthma.
价 格:¥电议型 号:T11581产 地:美洲
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T12071MKC9989MKC9989
MKC9989 is an inhibitor of Hydroxy aryl aldehydes (HAA).
价 格:¥电议型 号:T12071产 地:美洲
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T13066TAK-071TAK-071
TAK-071 is a potent, novel and highly selective modulator of muscarinic acetylcholine receptor 1 (M1R) positive allosteric(EC50 is 520 nM).
价 格:¥电议型 号:T13066产 地:美洲
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T13071TalsaclidineTalsaclidine
Talsaclidine is an agonist of muscarinic with preferential neuron-stimulating properties. Talsaclidine is a full agonist at the M1 subtype, and as a partial agonist at the M2 and M3 subtypes.
价 格:¥电议型 号:T13071产 地:美洲
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T14071A-385358A-385358
A-385358 is a Bcl-XL inhibitor. For Bcl-XL and Bcl-2, the Kis values are 0.80 and 67 nM, respectively.
价 格:¥电议型 号:T14071产 地:美洲
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T14547JWG-071JWG-071
JWG-071 is the first reported kinase-selective chemical probe for ERK5. JWG-071 will be a much-needed chemical probe for deconvoluting ERK5 and BRD4 pharmacology[1]. JWG-071 improves ERK5 activity and BRD4 selectivity.
价 格:¥电议型 号:T14547产 地:美洲
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T1751EliprodilEliprodil,SL-820715,
Eliprodil(SL-820715), a non-competitive NR2B-NMDA receptor antagonist(IC50: 1 uM), less effective for NR2A- and NR2C-containing receptors(IC50> 100 uM). It has been used in trials studying the treatment of Parkinson Disease and Movement Disorders.
价 格:¥电议型 号:T1751产 地:美洲
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T19071TMBTMB,BM blue,Sure Blue TMB
TMB (BM blue) is a chromogenic substrate used in staining procedures in immunohistochemistry and a visualizing reagent used in ELISA.
价 格:¥电议型 号:T19071产 地:美洲
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T2071MCOPPB trihydrochlrideMCOPPB trihydrochlride,MCOPPB 3HCl,MCOPPB triHydrochloride
MCOPPB trihydrochlride is a nociceptin receptor agonist.
价 格:¥电议型 号:T2071产 地:美洲
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T50714-Methyl-2-oxovaleric acid4-Methyl-2-oxovaleric acid,4-Methyl-2-oxopentanoic acid,
4-Methyl-2-oxopentanoic acid is an abnormal metabolite that arises from the incomplete breakdown of branched-chain amino acids. It is both a neurotoxin and a metabotoxin.
价 格:¥电议型 号:T5071产 地:美洲
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T5450DL-071-ITDL-071-IT,Afurolol Hydrochloride,DL 071 IT
DL 071-IT is a potent non-selective beta-adrenoceptor antagonist. DL 071 IT showed intrinsic sympathomimetic activity and weak membrane stabilizing activity.
价 格:¥电议型 号:T5450产 地:美洲
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T6071ParbendazoleParbendazole,SKF 29044,
Parbendazole is a potent inhibitor of microtubule assembly(EC50 : 8.79 nM).Parbendazole is a carbamate ester-amine. It finds applications in control or treatment of nematode infestations.
价 格:¥电议型 号:T6071产 地:美洲
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T6108Ki16425Ki16425,Debio 0719,
Ki16425 is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 with Ki of 0.34 μM, 6.5 μM and 0.93 μM, respectively.
价 格:¥电议型 号:T6108产 地:美洲
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T6278SotrastaurinSotrastaurin,AEB071,
Sotrastaurin is a potent pan-PKC inhibitor (Kis: 0.95/0.64/2.1/3.2/1.8/0.22 nM for PKCα/βI/δ/ε/η/θ).
价 格:¥电议型 号:T6278产 地:美洲
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T84293SSR 180;化合物 SSR 180SSR180711;SSR180711
SSR 180 is a potent and subtype-selective α7 agonist with applications in the study of Alzheimer;s disease and schizophrenia.
价 格:¥电议型 号:T84293产 地:中国大陆
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T83071Antifungal agent 62;化合物 Antifungal agent 62Antifungal agent 62
Compound 3a (Antifungal agent 62) exhibits potent fungicidal properties, particularly against Fusarium oxysporum f.sp. cucumerinum, and is utilized in antiviral and fungicidal research [1].
价 格:¥电议型 号:T83071产 地:中国大陆
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T82964ARUK2007145;化合物 ARUK2007145ARUK2007145
ARUK2007145 is a potent, cell-active inhibitor targeting both PI5P4Kα and PI5P4Kγ isoforms with pIC50 values of 7.3 and 8.1, respectively [1].
价 格:¥电议型 号:T82964产 地:中国大陆