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TP1862L[Sar9] Substance P acetate(77128-75-7 free base)[Sar9] Substance P acetate(77128 75 7 free base),[Sa
[Sar9]-Substance P acetate is one of NK-1 receptor agonist. The action of SP on progesterone metabolism was mimicked by the rNK1-specific agonist [Sar-9,Met(O2)11]-SP.
价 格:¥电议型 号:TP1862L产 地:中国大陆
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T7128TH-257LIM Kinase (LIMK),LIMKs,Inhibitor,TH-257,inhibit,TH257
TH 257 is a Potent and selective allosteric LIMK 1/2 inhibitor(LIMK1 and LIMK2, IC50 of 84 nM and 39 nM).
价 格:¥电议型 号:T7128产 地:中国大陆
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TN71284,6,3’,4’-Tetrahydroxyaurone
4,6,3´,4´-Tetrahydroxyaurone is a flavonoid from the herbs of Heleocharis dulcis.
价 格:¥电议型 号:TN7128产 地:中国大陆
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T16710MericitabineRG 7128;R-7128;PSI 6130 diisobutyrate
Mericitabine is a nucleoside HCV NS5B polymerase inhibitor. It acts as an RNA chain terminator and prevents the elongation of RNA transcripts during replication.
价 格:¥电议型 号:T16710产 地:中国大陆
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T16710MericitabineMericitabine,RG 7128,R-7128
Mericitabine is a nucleoside HCV NS5B polymerase inhibitor. It acts as an RNA chain terminator and prevents the elongation of RNA transcripts during replication.
价 格:¥电议型 号:T16710产 地:美洲
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T77128Pacmilimab;化合物 PacmilimabPacmilimab
Pacmilimab (CX-072) is a potent PD-L1 inhibitor. Pacmilimab shows antitumor activity [1] .
价 格:¥电议型 号:T77128产 地:中国大陆
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T712899-O-Demethyltrigonostemone;化合物 9-O-Demethyltrigonostemone9-O-Demethyltrigonostemone
9-O-Demethyltrigonostemone is a natural IDO1 inhibitor, cytotoxic and antiplasmodial agent from the Roots of Strophioblachia fimbricalyx.
价 格:¥电议型 号:T71289产 地:中国大陆
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T71288Phenylbutazone-d9;化合物 Phenylbutazone-d9Phenylbutazone-d9
Phenylbutazone-d9 is intended for use as an internal standard for the quantification of phenylbutazone by GC- or LC-MS. Phenylbutazone is a non-steroidal anti-inflammatory drug and an inhibitor of the peroxidase activity of COX (IC50 = ~100 ?M in the presence of hydrogen peroxide). It also inhibits prostaglandin I synthase (IC50 = ~25 ?M in the presence of hydrogen peroxide). Phenylbutazone (2 mg/kg) reduces increases in type II collagen levels in the inflamed joints of an equine model of LPS-in
价 格:¥电议型 号:T71288产 地:中国大陆
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T71287CDKI-83;化合物 CDKI-83CDKI-83
CDKI-83 is a potent CDK9 inhibitor. The compound shows effective anti-proliferative activity in human tumour cell lines with GI50 <1 μM, and is capable of inducing apoptosis in A2780 human ovarian cancer cells as determined by the activated caspase-3, Annexin V/PI double staining and accumulated cells at the sub-G1 phase of cellcycle. The research results suggest that combined inhibition of CDK9 and CDK1 may result in the effective induction of apoptosis and CDKI-83 has the potential to be devel
价 格:¥电议型 号:T71287产 地:中国大陆
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T71286Guaifenesin-d3;化合物 Guaifenesin-d3Guaifenesin-d3
Guaifenesin-d3 is intended for use as an internal standard for the quantification of guaifenesin by GC- or LC-MS. Guaifenesin is an expectorant. It inhibits production of mucin 5AC (MUC5AC), reduces mucus viscosity and elasticity, and increases the mucociliary transport rate of endogenous particles in primary human tracheobronchial epithelial cells in a concentration-dependent manner. Guaifenesin increases phenol red secretion, a marker of expectorant activity, in rats.3 Formulations containing
价 格:¥电议型 号:T71286产 地:中国大陆
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T71285Metaxalone-d6;化合物 Metaxalone-d6Metaxalone-d6
Metaxalone-d6 is intended for use as an internal standard for the quantification of metaxalone by GC-or LC-MS. Metaxalone is a skeletal muscle relaxant. It inhibits the proliferation of, and induces apoptosis in, RAW 264.7 cells in vitro when used at concentrations ranging from 1 to 100 ?M. Metaxalone also reduces LPS-induced increases in COX-1, COX-2, and NF-kB levels and inhibits LPS-induced production of TNF-α, IL-6, and prostaglandin E2 in RAW 264.7 cells. Formulations containing metaxalone
价 格:¥电议型 号:T71285产 地:中国大陆
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T71284Glimepiride urethane;化合物 Glimepiride urethaneGlimepiride urethane
Glimepiride urethane is a third generation sulfonylurea compound, which increases the release of insulin from pancreatic beta cells. In addition, glimepiride increases the activity of intracellular insulin receptors. Glimepiride increases osteoblast proliferation and differentiation, which is thought to be related to its ability to activate the PI3K and Akt pathway. Furthermore, Glimepiride enhances intrinsic peroxisome proliferator-activated receptor γ activity. Glimepiride also increases prote
价 格:¥电议型 号:T71284产 地:中国大陆
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T71283JNJ-40929837;化合物 JNJ-40929837JNJ-40929837
JNJ-40929837 is an oral inhibitor of LTA4 hydrolase, which catalyzes LTB4 production.
价 格:¥电议型 号:T71283产 地:中国大陆
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T71282ECANE;化合物 ECANEECANE
ECANE has the ability to chelate and mobilize cadmium in vivo, making it a good antagonist for cadmium intoxication.
价 格:¥电议型 号:T71282产 地:中国大陆
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T71281Nerispirdine;化合物 NerispirdineNerispirdine
Nerispirdine is a biochemical that inhibits batrachotoxin binding to voltage-dependent sodium channels.
价 格:¥电议型 号:T71281产 地:中国大陆
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T71280S 8308;化合物 S 8308S 8308
S 8308 is a weak, but specific and competitive, non-peptide antagonist of AII exerting its inhibitory action at the receptor level.
价 格:¥电议型 号:T71280产 地:中国大陆
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T7128TH-257;化合物TH 257TH 257;TH 257
TH-257 is a Potent and selective allosteric LIMK 1/2 inhibitor(LIMK1 and LIMK2, IC50 of 84 nM and 39 nM).
价 格:¥电议型 号:T7128产 地:中国大陆
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T68293MK-7128;化合物 MK-7128MK-7128
MK-7128 is a CB1 receptor inverse agonist.
价 格:¥电议型 号:T68293产 地:中国大陆
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T671282-Chloro-1-(2-ethoxyethyl)-1H-benzo[d]imidazole;化合物 2-Chloro-1-(2-ethoxyethyl)-1H-benzo[d]imidazole2
2-Chloro-1-(2-ethoxyethyl)-1H-benzo[d]imidazole is a useful organic compound for research related to life sciences. The catalog number is T67128 and the CAS number is 87233-54-3.
价 格:¥电议型 号:T67128产 地:中国大陆
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T37128Chemerin-9, Mouse;Chemerin-9, MouseChemerin-9, Mouse
Chemokine-like receptor 1 (CMKLR1) agonist (EC50 = 42 nM). Corresponds to C-terminal of full length mouse Chemerin, amino acids 148 - 156.
价 格:¥电议型 号:T37128产 地:中国大陆