当前位置：易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型：会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累，可浏览访问
(41-90)良好信誉积累，可接洽商谈
(91+ )优质信誉积累，可持续信赖
易推广会员：5年
工商认证 【已认证】
最后认证时间：
注册号： 【已认证】
法人代表： 【已认证】
企业类型：生产商 【已认证】
注册资金：人民币万 【已认证】
产品数：86101
参观次数：3500411
自主品牌
已选条件
-
T9524Lanthanum trichlorideLanthanum trichloride
Lanthanum trichloride can be used as an analytical reagent and can be used as a raw material for extracting metal lanthanum and as a petroleum cracking catalyst. Lanthanum chloride also has a certain role in the field of medicine. For example, studies have shown that the antagonistic effect of lanthanum chloride on endotoxin (LPS) in vivo effects has a certain impact on the search for new effective endotoxin antagonists, providing experimental evidence for the prevention and treatment of endotox
价 格：￥电议型 号：T9524产 地：中国大陆
-
T13957VerilopamVerilopam
Verilopam displays analgesic activities and can be used in pain studies.
价 格：￥电议型 号：T13957产 地：中国大陆
-
TP1365LParasin I acetate(219552-69-9 free base)Parasin I acetate(219552699 free base),Parasin I acetate(219
Parasin I acetate is a potent 19-residue antimicrobial peptide isolated from the skin mucus of wounded catfish (Parasilurus asotus).
价 格：￥电议型 号：TP1365L产 地：中国大陆
-
T9595LP-261NCI-H522,tubulin polymerization,tumor,SW-620,BXPC-3,H522,anti-mitotic,inhibit,LP261,MCF-7,Inhi
LP-261 is a novel tubulin targeting anticancer agent that binds at the colchicine site on tubulin, inducing G2/M arrest.
价 格：￥电议型 号：T9595产 地：中国大陆
-
T29522LN-[(1S)-5-tert-butyl-2,3-dihydro-1H-inden-1-yl]-N’-1H-indazol-4-ylurea(S)1(5(tertbutyl)2,3dihydro1Hi
N-[(1S)-5-tert-butyl-2,3-dihydro-1H-inden-1-yl]-N´-1H-indazol-4-ylurea is a potent TRPV1 antagonist, blocking activation of TRPV1 by capsaicin with the IC50 of 123 nM.
价 格：￥电议型 号：T29522L产 地：中国大陆
-
T9594BI-187004BI187004,BI 187004
BI-187004 is an 11β-hydroxysteroid dehydrogenase 1 inhibitor.
价 格：￥电议型 号：T9594产 地：中国大陆
-
T6S1495Ginsenoside Rk3inhibit,Nuclear factor-κB,Inhibitor,Ginsenoside Rk3,Ginsenoside Rk 3,NF-κB,Ginsenosid
1. Ginsenoside Rk3 and Rh4 could have a role in treating inflammatory diseases. 2. Ginsenoside Rk3 is often used as a major ingredient of the compound preparation for ischemic heart diseases.
价 格：￥电议型 号：T6S1495产 地：中国大陆
-
T6849UprosertibGSK-2141795,GSK 2141795,Uprosertib,inhibit,Akt,Inhibitor,PKB,Protein kinase B
Uprosertib (GSK2141795) is a selective, ATP-competitive, and orally bioavailable Akt inhibitor with IC50 of 180 nM, 328 nM, and 38 nM for Akt 1, 2 and 3, respectively. Phase 2.
价 格：￥电议型 号：T6849产 地：中国大陆
-
T9517ArprinocideArprinocide
Arprinocid is an inhibitor of hypoxanthine-guanine transport
价 格：￥电议型 号：T9517产 地：中国大陆
-
T39573GSK251GSK251,GSK-251
GSK251 is a highly potent, highly selective, orally bioavailable inhibitor of PI3Kδ with a novel binding mode.
价 格：￥电议型 号：T39573产 地：中国大陆
-
T60951Molnupiravir
Molnupiravir (EIDD-2801) is a prodrug of the ribonucleoside analog EIDD-1931 which is orally bioavailable. Molnupiravir can be used in COVID-19, seasonal and pandemic influenza research that has broad spectrum antiviral activity against multiple coronaviruses and influenza virus, for example, SARS-CoV-2, MERS-CoV, SARS-CoV [1][2].
价 格：￥电议型 号：T60951产 地：中国大陆
-
T21955GQ-16PPAR,Inhibitor,reduced adipogenic actions,PPARγ,GQ-16,insulin sensitization,inhibit,Peroxisome
GQ-16 is a partial agonist of PPARγ with a Ki of 160 nM. GQ-16 reduces adipogenic actions and promotes insulin Sensitization without weight gain.
价 格：￥电议型 号：T21955产 地：中国大陆
-
T9500M435-1279M435 1279,M4351279
M435-1279 is a UBE2T inhibitor. M435-1279 blocks UBE2T-mediated degradation of RACK1, leading to inhibit the hyperactivation of Wnt/β-catenin signaling pathway.
价 格：￥电议型 号：T9500产 地：中国大陆
-
T9950ElteN378ElteN378
ElteN378 is a highly potent synthetic inhibitor of FKBP12 with Ki of 0.5 nM, a low atomic weight ligand with affinity comparable to that of the macrolide Rapamycin.
价 格：￥电议型 号：T9950产 地：中国大陆
-
T7617LNeurotensin(8-13) 3TFA(60482-95-3(free base))Neurotensin(813) 3TFA(60482953(free base)),Neurotensin(
Neurotensin(8-13)(3TFA) is Neurotensin (NT) fragment, Neurotensin(8-13) results in a decrease in cell-surface NT1 receptors (NTR1) density.
价 格：￥电议型 号：T7617L产 地：中国大陆
-
T8895Altenusininhibit,Altenusin,Alutenusin,Inhibitor
Altenusin is a natural nonsteroidal fungal metabolite, as a novel selective agonist of FXR with an EC50 value of 3.2 ± 0.2 μM.
价 格：￥电议型 号：T8895产 地：中国大陆
-
T6610NSC-207895XI006,MDMX,p53,LPS,Inhibitor,XI 006,MDM2,inhibit,MDM-2/p53,NSC-207895,NSC207895
NSC 207895 suppresses MDMX with IC50 of 2.5 μM, leading to enhanced p53 stabilization/activation and DNA damage, and also regulates MDM2, an E3 ligase.
价 格：￥电议型 号：T6610产 地：中国大陆
-
T8957LCRT0066101 dihydrochloride(956121-30-5 free base)CRT-0066101 dihydrochloride(956121-30-5 free base),
CRT0066101 dihydrochloride is an inhibitor of PKD.
价 格：￥电议型 号：T8957L产 地：中国大陆
-
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
-
TP1953LPG 931 acetatePG 931 acetate
PG-931 acetate is a potent agonist of melanocortin 4 (MC4) receptors.
价 格：￥电议型 号：TP1953L产 地：中国大陆
