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产品数:86101
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T8439Clobenpropit dihydrobromideApoptosis,inhibit,Clobenpropit dihydrobromide,histamine H3R,antagonist,in
Clobenpropit dihydrobromide is a potent antagonist and inverse agonist of histamine H3R (histamine H3LR,pEC50 of 8.07)
价 格:¥电议型 号:T8439产 地:中国大陆
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TJS03145,7-Dihydroxy-4-methylcoumarinBacterial,inhibit,Fungal,Inhibitor,5,7Dihydroxy4methylcoumarin,5,7 Dih
5,7-Dihydroxy-4-methylcoumarin inhibits human neutrophil oxidative metabolism and elastase activity. 5,7-Dihydroxy-4-methylcoumarin has in vitro platelet antiaggregatory property. 5,7-Dihydroxy-4-methylcoumarin shows inhibition of the cyclooxygenase pathway.
价 格:¥电议型 号:TJS0314产 地:中国大陆
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TN1012LFebrifugine dihydrochlorideInhibitor,Parasite,Febrifugine dihydrochloride,antimalarial,alkaloid,Quin
Febrifugine dihydrochloride is a biochemical with therapeutic activity regarding malaria, cancer, fibrosis and inflammatory diseases.
价 格:¥电议型 号:TN1012L产 地:中国大陆
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T14362LAY 9944 dihydrochloride1(2chlorophenyl)N[[4[(2chlorophenyl)methylaminomethyl]cyclohexyl]methyl]metha
AY 9944 dihydrochloride is a intermediate.
价 格:¥电议型 号:T14362L产 地:中国大陆
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T9084Cetirizine Impurity B dihydrochlorideinhibit,Cetirizine Impurity B,Inhibitor,Cetirizine Impurity B d
Cetirizine Impurity B dihydrochloride is an impurity of Cetirizine dihydrochloride. Cetirizine is a second-generation antihistamine. Cetirizine is a specific, orally active and long-acting histamine H1-receptor antagonist. Cetirizine marks antiallergic properties and inhibits eosinophil chemotaxis during the allergic response.
价 格:¥电议型 号:T9084产 地:中国大陆
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T69811-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid1Methyl6oxo1,6dihydropyridine3carboxylic acid,In
Nudifloric Acid is from Cordyceps bassiana. Nudifloric Acid targets to block AP-1-mediated luciferase activity, implying it has an anti-inflammatory function.
价 格:¥电议型 号:T6981产 地:中国大陆
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T79823,6-Dihydroxyflavoneinhibit,Inhibitor,caspase cascade,cell viability,oxidative stress,3,6-DHF,Apopto
3,6-Dihydroxyflavone suppresses the epithelial-mesenchymal transition in breast cancer cells by inhibiting the Notch signaling pathway.
价 格:¥电议型 号:T7982产 地:中国大陆
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T86112,3-dihydro-1H-indene-5-sulfonamide2,3 dihydro 1H indene 5 sulfonamide,2,3dihydro1Hindene5sulfonamid
2,3-dihydro-1H-indene-5-sulfonamide is Carbonic anhydrase 12 (human) inhibitor.
价 格:¥电议型 号:T8611产 地:中国大陆
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T32613LCB 03-0110 dihydrochlorideLCB 030110 dihydrochloride,LCB 03 0110 dihydrochloride
LCB 03-0110 Dihydrochloride is a potent inhibitor of the c-Src kinase (IC50 = 1.3 nM) and tyrosine kinases in the BTK and SYK family, as well as in the DDR2 family. It inhibits LPS-induced activation of macrophages and TGF-β1-induced activation of fibroblasts in vitro, inhibits activation of macrophages and fibroblasts, and inhibits scarring in wound healing models.
价 格:¥电议型 号:T32613产 地:中国大陆
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T6571Lomerizine dihydrochlorideCa2+ channels,Ca channels,inhibit,Lomerizine,KB 2796,KB2796,Lomerizine dih
Lomerizine dihydrochloride is an antagonist of L- and T-type voltage-gated calcium channels used to treat migraine.
价 格:¥电议型 号:T6571产 地:中国大陆
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T9121AG-636inhibit,oral,AG 636,AG-636,reversible,DHODH,anticancer,AG636,Inhibitor,Dihydroorotate Dehydrog
AG-636 is a potent, reversible, selective and orally active DHODH inhibitor(IC50 of 17 nM). It has strong anticancer effects.
价 格:¥电议型 号:T9121产 地:中国大陆
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T85846-Phenyldihydropyrimidine-2,4(1h,3h)-dione6Phenyldihydropyrimidine2,4(1h,3h)dione,6 Phenyldihydropyr
6-Phenyldihydropyrimidine-2,4(1h,3h)-dione targets the polypyrimidine tract-binding protein 1 isoform a (human)
价 格:¥电议型 号:T8584产 地:中国大陆
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TN6785DihydrocatalpolDihydrocatalpol
Dihydrocatalpol,a natural product obtained from the herbs of Rehmannia glutinosa.
价 格:¥电议型 号:TN6785产 地:中国大陆
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TN7058DihydrolapachenoleInhibitor,Dihydrolapachenole,inhibit
dihydrolapachenol is a natural isolated from the heartwood of T. chrysantha.
价 格:¥电议型 号:TN7058产 地:中国大陆
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T6951Pramipexole dihydrochloride hydratetransient,Pramipexole dihydrochloride,Pramipexole dihydrochloride
Pramipexole Dihydrochloride is the hydrochloride salt of pramipexole, a benzothiazole derivative. As a nonergot dopamine agonist, pramipexole binds to D2 and D3 dopamine receptors in the striatum and substantia nigra of the brain.
价 格:¥电议型 号:T6951产 地:中国大陆
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T35341NVP-BSK805 dihydrochloride
NVP-BSK805 dihydrochloride is an effective and selective inhibitor of JAK2 with IC50s of 0.5 nM, 10.76 nM, 18.68 nM, and 31.63 nM for JAK2, TYK2, JAK3, and JAK1.
价 格:¥电议型 号:T35341产 地:中国大陆
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T7117Sapropterin dihydrochloride(6R)-BH4,Sapropterin,Inhibitor,inhibit,Sapropterin dihydrochloride
Sapropterin dihydrochloride is phenylalanine hydroxylase agonist that is approved for the treatment of BH4 responsive PKU.
价 格:¥电议型 号:T7117产 地:中国大陆
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T13890SMARCA-BD ligand 1 for Protac dihydrochlorideSMARCABD ligand 1 for Protac dihydrochloride,SMARCA BD
SMARCA-BD ligand 1 for Protac dihydrochloride binds to the BAF ATPase subunits SMARCA2, and used for degrading SMARCA2, based on PROTAC.
价 格:¥电议型 号:T13890产 地:中国大陆
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T10837Clocapramine dihydrochloride hydrateClocapramine dihydrochloride hydrate
Clocapramine dihydrochloride hydrate is an antagonist of the 5-HT2A and D2 receptors.
价 格:¥电议型 号:T10837产 地:中国大陆