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T9159PBT-1033PBT 1033
PBT-1033(PBT-2) is a potential neuroprotective agent for the treatment of Alzheimer´s disease and Huntington´s disease.
价 格:¥电议型 号:T9159产 地:中国大陆
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T27854LSN2463359LSN2463359
LSN2463359 is a positive allosteric modulators of the mGlu5 receptor.
价 格:¥电议型 号:T27854产 地:中国大陆
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T8566AA92593Per1,AA-92593,Melanopsin,α-MSH,AA92593,inhibit,Inhibitor,OPN4,AA 92593,Melanoma,CHO
AA92593 has been used as a selective inhibitor of melanopsin.
价 格:¥电议型 号:T8566产 地:中国大陆
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T9520ALC-0159ALC0159,conjugate,lipid,vaccine,ALC 0159,ALC-0159,inhibit,excipient,Inhibitor
ALC-0159 is a polyethylene glycol (PEG) lipid conjugate that could be used as a vaccine excipient[1].
价 格:¥电议型 号:T9520产 地:中国大陆
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TN7059Deoxylimoninanticancer,Inhibitor,anti-inflammation,antinociception,Deoxylimonin,inhibit,MCF-7
Deoxylimonin is a triterpenoid isolated from grapefruit seeds.
价 格:¥电议型 号:TN7059产 地:中国大陆
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T9979WAY-302159Inhibitor,VEGFR,quinoline amide,inhibit,WAY 302159,HUVEC,Vascular endothelial growth facto
WAY-302159 is a VEGFR2 inhibitor.
价 格:¥电议型 号:T9979产 地:中国大陆
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T8959OS-3-106Inhibitor,inhibit,Dopamine Receptor,HEK 293 cells,self-administration,arylamide phenylpipera
OS-3-106 is a novel arylamide phenylpiperazines, as partial agonists at the D3R in the adenylyl cyclase inhibition assay.
价 格:¥电议型 号:T8959产 地:中国大陆
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T6599N6-methyladenosineN-6-methyladenosine,inhibit,N6-Methyladenosine,Inhibitor,Endogenous Metabolite,N6m
N6-Methyladenosine is a methylated adenine residue. N6-Methyladenosine is an endogenous urinary nucleoside product of the degradation of transfer ribonucleic acid (tRNA); urinary nucleosides are biological markers for patients with colorectal cancer.
价 格:¥电议型 号:T6599产 地:中国大陆
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TN2159Robustinealkaloid,phosphodiesterase,Phosphodiesterase (PDE),Robustine,PDE5A,inhibit,Inhibitor
Robustine is a natural product, exhibits inhibitory potency against human phosphodiesterase 5 (hPDE5A) in vitro.
价 格:¥电议型 号:TN2159产 地:中国大陆
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T6950PNU-120596pain,NSC216666,anti-hyperalgesia,inhibit,inflammatory,PNU 120596,PNU-120596,Nicotinic acet
PNU-120596 is a positive allosteric modulator of α7 nAChR with EC50 of 216 nM.
价 格:¥电议型 号:T6950产 地:中国大陆
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T25986Prinomide tromethaminePrinomide tromethamine
Prinomide tromethamine is an antirheumatic compound.
价 格:¥电议型 号:T25986产 地:中国大陆
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T37591IMP-1710IMP1710,IMP 1710
IMP-1710 is a selective UCH-L1 inhibitor with an IC50 value of 38 nM in a fluorescence polarization assay.
价 格:¥电议型 号:T37591产 地:中国大陆
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T6S0659Rhynchophyllineinhibit,Rhynchophylline,Nuclear factor-κB,Nuclear factor-kappaB,Inhibitor,NF-κB
1. Rhynchophylline can protect against ischemic damage, probably via regulating the Akt/mTOR pathway. 2. Rhynchophylline can protect against glutamate-induced neuronal death, can inhibit MA impairment in cultured neurons in vitro. 3. Rhynchophylline and isorhynchophylline have a non-competitive antagonistic effect on the NMDA-type ionotropic glutamate receptors, suggest that these alkaloids exert their protective action against ischemia-induced neuronal damage by preventing NMDA, muscarinic M1,
价 格:¥电议型 号:T6S0659产 地:中国大陆
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T9137SN-011inflammatory,ERIS,inhibit,Inhibitor,Stimulator of Interferon Genes,CDN,SN-011,STING,MITA,autoi
GUN35901 is a STING inhibitor, which inhibited the activation of the STING signal pathway and to prevent or treat a STING- mediated disease. It is a demethyl analogue of DUN99845.
价 格:¥电议型 号:T9137产 地:中国大陆
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T6659SB 415286inhibit,GSK-3,Inhibitor,Glycogen synthase kinase 3,Glycogen synthase kinase-3,Apoptosis,SB-
SB415286 is a potent GSK3α inhibitor with IC50/Ki of 78 nM/31 nM with equally effective inhibition of GSK-3β.
价 格:¥电议型 号:T6659产 地:中国大陆
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T11599Ibiglustat (L-Malic acid)
Ibiglustat (L-Malic acid) is a selective, brain-penetrant, and allosteric inhibitor of glucosylceramide synthase. Ibiglustat (L-Malic acid) can be used in studies about PD Parkinson’s disease, SRT in Fabry’s and Gaucher’s.
价 格:¥电议型 号:T11599产 地:中国大陆
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T5390BMS-599626 HydrochlorideBMS 599626 Hydrochloride,BMS599626 Hydrochloride
BMS-599626 Hydrochloride (AC480 Hydrochloride) is a selective and orally bioavailable inhibitor of HER1 and HER2, with IC 50 s of 20 and 30 nM, respectively. BMS-599626 Hydrochloride shows ~8-fold less potent to HER4 (IC 50 =190 nM), >100-fold to VEGFR2, c-Kit, Lck, MEK. BMS-599626 Hydrochloride inhibits tumor cell proliferation, and has potential to increase tumor response to radiotherapy [1] [2].
价 格:¥电议型 号:T5390产 地:中国大陆
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T6593ML324ML-324,Jumonji,periodontal,Cytomegalovirus,ML324,inhibit,simplex,CMV,Inhibitor,Herpes simplex v
ML324(IC50=920 nM) is a specific inhibitor of jumonji histone demethylase (JMJD2).
价 格:¥电议型 号:T6593产 地:中国大陆
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TQ0132A 419259 trihydrochlorideA 419259 trihydrochloride,Src,Inhibitor,inhibit
A 419259 trihydrochloride is an Src family kinases inhibitor (IC50s: 9 nM, 3 nM and 3 nM for Src, Lck and Lyn).
价 格:¥电议型 号:TQ0132产 地:中国大陆