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T6781BenzenesulfonamideInhibitor,inhibit,QSAR study,Benzenesulfonamide,carbonic anhydrases,Carbonic Anhyd
Benzenesulfonamide ia an inhibitor of carbonic anhydrases.
价 格:¥电议型 号:T6781产 地:中国大陆
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TQ01722’’-O-Rhamnosylicariside IIInhibitor,2’’ O Rhamnosylicariside II,inhibit,2’’ORhamnosylicariside II
2´´-O-Rhamnosylicariside II is beneficial for improving postmenopausal osteoporosis. It shows potent antioxidant activity, with IC50 values of 90.5 uM.
价 格:¥电议型 号:TQ0172产 地:中国大陆
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TPL03664-Biphenylcarboxylic acid4 Biphenylcarboxylic acid,4Biphenylcarboxylic acid
价 格:¥电议型 号:TPL0366产 地:中国大陆
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T94371-methoxycyclopropanecarboxylic acid1methoxycyclopropanecarboxylic acid,1 methoxycyclopropanecarboxy
1-methoxycyclopropanecarboxylic acid is an agonist of free fatty acid receptor 3 (FFAR3, human).
价 格:¥电议型 号:T9437产 地:中国大陆
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Fr212652-Methyl-2H-indazole-3-carboxylic acid
价 格:¥电议型 号:Fr21265产 地:中国大陆
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T8911methyl 5-(3,4-dimethoxyphenyl)isoxazole-3-carboxylatemethyl 5(3,4dimethoxyphenyl)isoxazole3carboxyla
methyl 5-(3,4-dimethoxyphenyl)isoxazole-3-carboxylate is a biochemical.
价 格:¥电议型 号:T8911产 地:中国大陆
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T9891PARP1-IN-8?poly ADP ribose polymerase,phthalazinone,PARP,inhibit,HFF cells,Lung adenocarcinoma,Inhib
PARP1-IN-8 is an effective inhibito of PARP1 (IC50 = 97 nM).
价 格:¥电议型 号:T9891产 地:中国大陆
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TMS2180ZeaxanthinEndogenous Metabolite,carotenoid,macula,inhibit,eye,tissues,Inhibitor,antioxidant,lipophil
1. Lutein and Zeaxanthin in neural tissue may have biological effects that include antioxidation, anti-inflammation, and structural actions. 2. Lutein and Zeaxanthin may be protective against eye disease because they absorb damaging blue light that enters the eye.
价 格:¥电议型 号:TMS2180产 地:中国大陆
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T643433-Methylcarbazole
3-Methylcarbazole is an carbazole alkaloid compound with anticancer effects.
价 格:¥电议型 号:T64343产 地:中国大陆
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TQ0054Purpureaside C化合物 Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate(Free ba
Purpureaside C is a phenolic glycoside with significant proinflammatory, immunomodulating and antimicrobial effects.
价 格:¥电议型 号:TQ0054产 地:中国大陆
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TN4661NodosinI. Japonicus,Isodon trichocarpus,inhibit,Nodosin,Inhibitor,diterpenoid
Nodosin has an anti-inflammatory function via inhibition of IL-2. Nodosin perfusion provides a potential protective effect by inducing HO-1 expression to attenuate ischemia/reperfusion injury in liver transplantation.
价 格:¥电议型 号:TN4661产 地:中国大陆
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TN71845,6-dibromo-1H-indole-3-carbaldehyde
5,6-dibromo-1H-indole-3-carbaldehyde is a marine derived natural products found in Smenospongia sp.
价 格:¥电议型 号:TN7184产 地:中国大陆
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TP1289Cardiotoxin Analog (CTX) IV (6-12) TFACardiotoxin Analog (CTX) IV (6 12) TFA,Cardiotoxin Analog (CTX
Cardiotoxin Analog (CTX) IV (6-12) TFA is a part peptide of Cardiotoxin Analog (CTX) IV. Cardiotoxin analogues IV isolated from the venom of Taiwan Cobra. CTX IV is an unique snake venom cardiotoxin[1].
价 格:¥电议型 号:TP1289产 地:中国大陆
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T21818Pregnenolone CarbonitrileCYPs,Cytochrome P450,P4503A,orally,Pregnenolone Carbonitrile,Pregnenolone 1
Pregnenolone Carbonitrile is an activator of rodent-PXR and induces the expression of CYP3A.
价 格:¥电议型 号:T21818产 地:中国大陆
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T7914Acenaphthylenearomatic,hydrocarbon,polycyclic,Acenaphthylene,Inhibitor,inhibit
Acenaphthylene is environmental polycyclic aromatic hydrocarbon (PAH)pollutants
价 格:¥电议型 号:T7914产 地:中国大陆
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T9579GLP-1 receptor agonist 9GLP 1 receptor agonist 9,Inhibitor,inhibit,Glucagon Receptor,GLP-1 receptor
1H-Benzimidazole-6-carboxylic acid is a GLP-1 receptor agonist.
价 格:¥电议型 号:T9579产 地:中国大陆
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TN71759H-Carbazole, 3,6-diiodo-
9H-Carbazole, 3,6-diiodo- is a marine derived natural products found in Kyrtuthrix maculans.
价 格:¥电议型 号:TN7175产 地:中国大陆
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T9281(S)-2-((R)-3-(4-chlorophenyl)-N’-((4-chlorophenyl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carbo
(S)-2-((R)-3-(4-chlorophenyl)-N’-((4-chlorophenyl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidamido)-3-methylbutanamide is a cannabinoid receptor antagonist/inverse agonist.
价 格:¥电议型 号:T9281产 地:中国大陆
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T7806Licarbazepinepartial,Licarbazepine,Sodium Channel,Na channels,voltage,Inhibitor,sodium,seizures,stab
Licarbazepine is the pharmacologically active metabolite of oxcarbazepine, a drug indicated for the treatment of partial seizures and bipolar disorders.
价 格:¥电议型 号:T7806产 地:中国大陆
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T9019JHU37152JHU37152,inhibit,hM3Dq,Clozapine,Inhibitor,DREADD,Muscarinic acetylcholine receptor,mAChR,hM
JHU 37152 is a Designer Receptors Exclusively Activated by Designer Drug (DREADD) agonist with Ki of 1.8 nM and 8.7 nM for human muscarinic acetylcholine M3 receptors (hM3Dq) and hM4Di in vitro, respectively. And EC50 values are 5 nM and 0.5 nM for hM3Dq and hM4Di in fluorescent and BRET-based assays in HEK-293 cells, respectively.
价 格:¥电议型 号:T9019产 地:中国大陆