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：3233751
自主品牌
已选条件
-
T88332-chloro-5-(16,18-dioxo-17-azapentacyclo[6.6.5.0~2,7~.0~9,14~.0~15,19~]nonadeca-2,4,6,9,11,13-hexaen
2-chloro-5-(16,18-dioxo-17-azapentacyclo[6.6.5.0~2,7~.0~9,14~.0~15,19~]nonadeca-2,4,6,9,11,13-hexaen-17-yl)benzoic acid is a chemical compound
价 格：￥电议型 号：T8833产 地：中国大陆
-
TN1157(-)-Menthoneinhibit,()Menthone,Inhibitor,( ) Menthone
(-)-Menthone is a natural product.
价 格：￥电议型 号：TN1157产 地：中国大陆
-
TP1526L1Fibronectin CS1 Peptide acetateFibronectin CS1 Peptide acetate,Fibronectin CS-1 Peptide acetate
CS1 peptide is present within type III homology connecting segment (IIICS) as well as C-274 (cell-binding domain). Fibronectin CS1 Peptide lacks the Arg-Gly-Asp-containing domain, actively inhibits tumor metastases in spontaneous and experimental metastasis models.
价 格：￥电议型 号：TP1526L1产 地：中国大陆
-
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
-
T26815BILB-1941
BILB-1941 is an inhibitor of HCV NS5B polymerase and can be used in studies about HCV infection.
价 格：￥电议型 号：T26815产 地：中国大陆
-
T15387GLP-1R Antagonist 1GLP 1R Antagonist 1,GLP1R Antagonist 1
GLP-1R Antagonist 1 is an orally active, CNS penetrant and non-competitive glucagon-like peptide 1 receptor (GLP-1R) antagonist (IC50: 650 nM).
价 格：￥电议型 号：T15387产 地：中国大陆
-
T15000Cort108297Cort108297,Cort-108297
Cort108297 is a specific antagonist of the glucocorticoid receptor with a high affinity for GRs (Ki: 0.45 nM).
价 格：￥电议型 号：T15000产 地：中国大陆
-
T8115MenthofuranInhibitor,peppermint oil biosynthesis,inhibit,monoterpene reductase,Menthofuran,Drug Meta
Menthofuran is a natural product.
价 格：￥电议型 号：T8115产 地：中国大陆
-
T15612JH-VIII-157-02CD246,Cluster of differentiation 246,inhibit,Anaplastic lymphoma kinase,Anaplastic lym
JH-VIII-157-02 is an inhibitor of ALK and inhibits echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) with IC50s of 2 nM for EML4-ALK G1202R, EML4-ALKwt, EML4-ALK C1156Y, EML4-ALK F1174L, and EML4-ALK F1174L.
价 格：￥电议型 号：T15612产 地：中国大陆
-
T60156PBRM1-BD2-IN-2PBRM1BD2IN2
PBRM1-BD2-IN-2 is a selective and cell-active polybromo-1 (PBRM1) bromodomain inhibitor. PBRM1-BD2-IN-2 has binding affinity and inhibitory activity for PBRM1-BD2 with Kd and IC50 values of 9.3 μM and 1.0 μM, respectively. PBRM1-BD2-IN-2 can be used for the research of cancer.
价 格：￥电议型 号：T60156产 地：中国大陆
-
TP1158Copper tripeptidehuman plasma,Copper tripeptide,inhibit,chemoattractant,fibroblast,endothelial,prote
Copper peptide GHK-Cu is a naturally occurring copper complex of the tripeptide glycyl-L-histidyl-L-lysine. The tripeptide has strong affinity for copper(II) and was first isolated from human plasma. It can be found also in saliva and urine.
价 格：￥电议型 号：TP1158产 地：中国大陆
-
T9699TAK-615LPA1,fibrosis,LPL Receptor,Lysophospholipid Receptor,TAK615,modulator,TAK-615,NAM,inhibit,pul
TAK-615 is commonly used to study pulmonary fibrosis and is a negative allosteric modulator of LPA1 receptors.
价 格：￥电议型 号：T9699产 地：中国大陆
-
T7309TAS-103 dihydrochlorideBMS247615,Topoisomerase,TAS-103,TAS103,inhibit,TAS 103 dihydrochloride,BMS-24
TAS-103 (dihydrochloride) is a novel anticancer agent targeting both topoisomerase (Topo) I and Topo II.
价 格：￥电议型 号：T7309产 地：中国大陆
-
TQ0159U-73343U-73343,Inhibitor,U73343,Phospholipase,inhibit
U 73343 is an inactive analog of U 73122 and can be used as a negative control. It dose-dependently inhibits acid secretion irrespective of the stimulant. It is a phospholipase C (PLC) and 5-LO (5-lipoxygenase) inhibitor with an IC50 of 1-2.1 μM for PLC.
价 格：￥电议型 号：TQ0159产 地：中国大陆
-
T7154trans-trans-Muconic acidtranstransMuconic acid,Endogenous Metabolite,inhibit,Inhibitor,trans trans M
trans-trans-Muconic acid is a urinary metabolite of benzene.
价 格：￥电议型 号：T7154产 地：中国大陆
-
T80154-METHOXYCHALCONE4 METHOXYCHALCONE,4METHOXYCHALCONE
4-METHOXYCHALCONE is a natural compound that enhanced adipocyte differentiation,
价 格：￥电议型 号：T8015产 地：中国大陆
-
T15608Jarin-1Jarin 1,Jarin1
Jarin-1 is a jasmonic acid-amido synthetase (JAR1) inhibitor (IC50: 3.8 μM). Jarin-1 specific suppresses bioactive JA biosynthesis in Arabidopsis and other plants.
价 格：￥电议型 号：T15608产 地：中国大陆
-
T8484JSH-150CDK,inhibit,Cyclin dependent kinase,Inhibitor,JSH150,JSH-150,JSH 150
JSH-150 is a highly selective CDK9 inhibitor(IC50 : 1 nM).
价 格：￥电议型 号：T8484产 地：中国大陆
-
T7152Ravuconazoleinhibit,ER30346,BMS207147,Ravuconazole,BMS 207147,Fungal,ER 30346,Inhibitor
Ravuconazole is a potent triazole antifungal that potently inhibits a wide range of fungi.
价 格：￥电议型 号：T7152产 地：中国大陆
-
TP1942L1pep2-AVKI acetate(1315378-69-8 free base)pep2AVKI acetate(1315378698 free base),pep2 AVKI acetate(13
Inhibitor peptide that selectively disrupts binding of the AMPA receptor subunit GluA2 (at the C-terminal PDZ site) to protein interacting with C kinase (PICK1). Does not affect binding of GluA2 to GRIP or ABP and does not increase AMPA current amplitude or affect long term depression (LTD).
价 格：￥电议型 号：TP1942L1产 地：中国大陆
