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T3112Verteporfin维替泊芬;CL 318952;BPD-MA
Verteporfin, a benzoporphyrin derivative monoacid ring A, can inhibit the activity of YAP.
价 格:¥电议型 号:T3112产 地:中国大陆
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T3067TideglusibNP-12;NP031112
Tideglusib, a non-ATP competitive inhibitor of glycogen synthase kinase 3 (GSK-3), is with anti-inflammatory and neuroprotective activities.
价 格:¥电议型 号:T3067产 地:中国大陆
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T2S09732-Methoxycinnamic acidAI3-11206;o-Methoxycinnamic acid;2-甲氧基肉桂酸
1. 2-Methoxycinnamic acid can enhance inhibition of tyrosinase activity.
价 格:¥电议型 号:T2S0973产 地:中国大陆
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T2S0112yibeinoside A伊贝碱苷A;Sinpeinine-3-O-β-glucoside
Yibeinoside A is an alkaloid from Fritillaria pallidiflora.
价 格:¥电议型 号:T2S0112产 地:中国大陆
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T29112VPC171(2-氨基-4-(3-(三氟甲基)苯基)噻吩-3-基)(苯基)甲酮;VPC-171;VPC 171
VPC171 is a novel adenosine A1 receptor positive allosteric modulator (PAM).
价 格:¥电议型 号:T29112产 地:中国大陆
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T23383SR11237SR 11237
SR11237 is a Pan retinoid X receptor (RXR) agonist. SR11237 causes RXR/RXR homodimers to form and transactivate a reporter gene containing a RXR-response element.
价 格:¥电议型 号:T23383产 地:中国大陆
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T2125Trametinib曲美替尼;JTP-74057;GSK1120212
Trametinib is an ATP-noncompetitive inhibitor of MEK 1/2 (IC50s: 0.7/0.9 nM). It shows low inhibition for more than 180 kinases, including B-Raf, c-Raf, and MEK5.
价 格:¥电议型 号:T2125产 地:中国大陆
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T2112Fexinidazole非昔硝唑;HOE 239
Fexinidazole is an antiparasitic agent. It has activity against Trypanosoma cruzi, Tritrichomonas foetus, Trichomonas vaginalis, Entamoeba histolytica, Trypanosoma brucei, and Leishmania donovani. The biologically relevant active metabolites in vivo are t
价 格:¥电议型 号:T2112产 地:中国大陆
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T20112Triphenyl bismuthNSC 465;NSC465;NSC-465
Triphenyl bismuth is an additive for making biomedical resins visible on x-ray images and can be used as a radiopaque agent for orthopaedic bone cements.
价 格:¥电议型 号:T20112产 地:中国大陆
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T19112LSacubitril EnantiomerLCZ 696杂质A;ahu377 isomer 2;2R,4S-Sacubitril
Sacubitril Enantiomer is the enantiomer of Sacubitril which is a neprilysin inhibitor.
价 格:¥电议型 号:T19112L产 地:中国大陆
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T1811WH-4-023KIN001-112;Dual LCK/SRC inhibitor;KIN112
WH-4-023 is a potent and orally active Lck/Src inhibitor. It also potently inhibits SIK.
价 格:¥电议型 号:T1811产 地:中国大陆
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T1777Nintedanib尼达尼布;Intedanib;BIBF 1120
Nintedanib is an inhibitor of the receptor tyrosine kinases VEGFR/FGFR/PDGFR (IC50s: 13-34/37-610/59/65 nM for VEGFR1-3, FGFR1-4, and PDGFRα/β, respectively).
价 格:¥电议型 号:T1777产 地:中国大陆
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T17059TetrahydrouridineNSC 112907;NSC-112907;NSC112907;四氢尿苷
Tetrahydrouridine (THU) is a multidrug resistance modulator. It can be used in cancer treatment to make tumor cells more sensitive to radiation therapy. THU is a competitive cytidine deaminase(CDA) inhibitor that inhibits deamination in the catabolism of
价 格:¥电议型 号:T17059产 地:中国大陆
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T13324VUF11207 fumarate
VUF11207 fumarate is an agonist of CXCR7 and a high-potency ligand of CXCR7 (pKi: 8.1).
价 格:¥电议型 号:T13324产 地:中国大陆
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T13112L1Tat-NR2B9c acetateNA-1 acetate;Tat-NR2B9c acetate (500992-11-0 Free base)
Tat-NR2B9c acetate is a postsynaptic density-95 (PSD-95) inhibitor, with EC50 values of 6.7 nM and 670 nM for PSD-95d2 (PSD-95 PDZ domain 2) and PSD-95d1, respectively. Tat-NR2B9c acetate disrupts the PSD-95/NMDAR interaction, inhibiting NR2A and NR2B bin
价 格:¥电议型 号:T13112L1产 地:中国大陆
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T11298FLT3-IN-3
FLT3-IN-3 is an effective FLT3 inhibitor, and the IC50s of FLT3 WT and FLT3 D835Y are 13 and 8 nM, respectively.
价 格:¥电议型 号:T11298产 地:中国大陆
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T1129BenfotiamineBenzoylthiamine monophosphate;S-Benzoylthiamine O-monophosphate;苯磷硫胺
Benfotiamine is a synthetic S-acyl derivative of thiamine (vitamin B1), used as an antioxidant dietary supplement.
价 格:¥电议型 号:T1129产 地:中国大陆
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T11285FIDAS-5
FIDAS-5 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding. FIDAS-5 has anticancer activities. FIDAS-5 is a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC50 of 2.1 μM.
价 格:¥电议型 号:T11285产 地:中国大陆