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
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:3784074
已选条件
-
T62711OPC-14523 hydrochloride;OPC-14523 盐酸盐VPI 013 hydrochloride;VPI 013 hydrochloride
OPC-14523 hydrochloride (VPI 013 hydrochloride) is an orally active and potent sigma and 5-HT1A receptor agonist with antidepressant activity for the study of neurological disorders.
价 格:¥电议型 号:T62711产 地:中国大陆
-
T62603NVP-BBD130;化合物 NVP-BBD130NVP-BBD130
NVP-BBD130 is a stable, ATP-competitive, potent, orally active inhibitor of PI3K and mTOR.
价 格:¥电议型 号:T62603产 地:中国大陆
-
T6204QNZ;化合物QNZCAY10470|||EVP4593;CAY10470|||EVP4593
QNZ (EVP4593) (EVP4593) is an effective inhibitor of NF-κB activation and TNF-α production. The IC50 of QNZ for NF-κB and TNF-α is11 nM and 7 nM, respectively.
价 格:¥电议型 号:T6204产 地:中国大陆
-
T61653VPC-13789;化合物 VPC-13789VPC-13789
VPC-13789 is a highly potent, selective, and orally bioavailable antiandrogen compound that shows promise for studying and developing therapeutics for castration-resistant prostate cancer (CRPC). In LNCaP cells, VPC-13789 effectively inhibits the transcriptional activity of the androgen receptor (AR) with an IC50 value of 0.19 μM [1].
价 格:¥电议型 号:T61653产 地:中国大陆
-
T6118NVP-HSP990;化合物HSP990HSP990;HSP990
NVP-HSP990 (HSP990) is an effective and specific HSP90α/β inhibitor (IC50: 0.6 /0.8 nM).
价 格:¥电议型 号:T6118产 地:中国大陆
-
T6080NVP-AEW541;化合物NVP-AEW541AEW541;AEW541
NVP-AEW541 (AEW541), a potent inhibitor of IGF-1R(IC50=150 nM) and InsR(IC50=140 nM), exhibits excellent efficiency and specificity for IGF-1R in a cell-based assay.
价 格:¥电议型 号:T6080产 地:中国大陆
-
T6079NVP-ADW742;化合物NVP-ADW742ADW742|||ADW|||GSK 552602A;ADW742|||ADW|||GSK 552602A
NVP-ADW742 (ADW) is an IGF-1R inhibitor with IC50 of 0.17 μM, >16-fold more potent against IGF-1R than InsR; little activity to HER2, PDGFR, VEGFR-2, Bcr-Abl and c-Kit.
价 格:¥电议型 号:T6079产 地:中国大陆
-
T6072LBGT226;化合物BGT226BGT226 free base|||NVP-BGT226;BGT226 free base|||NVP-BGT226
BGT226 (NVP-BGT226) is a novel dual PI3K / mTOR inhibitor, it acts on PI3K α/β/γ with IC50 of 4 nM / 63 nM / 38 nM, respectively.
价 格:¥电议型 号:T6072L产 地:中国大陆
-
T6072BGT226 maleate;化合物BGT226BGT226|||NVP-BGT226 (maleate)|||NVP-BGT226;BGT226|||NVP-BGT226 (maleate)|||N
BGT226 maleate (NVP-BGT226) is a class I PI3K/mTOR inhibitor for PI3Kα/β/γ (IC50: 4/63/38 nM) .
价 格:¥电议型 号:T6072产 地:中国大陆
-
T60525VP-4556;化合物 VP-4556VP-4556
VP-4556 is a potent anti-methicillin-resistant Staphylococcus aureus ( MRSA ) agent that exhibits significant microbial growth inhibition against Staphylococcus aureus (ATCC 43300) (MIC = 8 μg/mL). VP-4556 inhibits methicillin‐resistant Staphylococcus aureus with growth inhibition >95% [1].
价 格:¥电议型 号:T60525产 地:中国大陆
-
T60506Vps34-IN-3;化合物 Vps34-IN-3Vps34-IN-3
Vps34-IN-3 is a potent, selective, and orally bioavailable inhibitor of VPS34 kinase .
价 格:¥电议型 号:T60506产 地:中国大陆
-
T60051VPC-18005;化合物VPC-18005VPC-18005
VPC-18005 is a luciferase inhibitor. VPC-18005 inhibits ERG-induced transcription and interacts directly with the ERG-ETS domain thereby disrupting the ERG binding to DNA.
价 格:¥电议型 号:T60051产 地:中国大陆
-
T5956VP3.15 dihydrobromide;化合物VP3.15 dihydrobromideVP3.15 dihydrobromide
VP3.15 dihydrobromide is a potent, orally bioavailable and CNS-penetrant dual phosphodiesterase (PDE7- glycogen synthase kinase (GSK)3 inhibitor(with IC50s of 1.59 μM , 0.88 μM,respectively.)
价 格:¥电议型 号:T5956产 地:中国大陆
-
T5555Siremadlin;化合物NVP-HDM 201NVP-HDM 201;NVP-HDM 201
Siremadlin (NVP-HDM 201) is a potent, orally bioavailable and highly specific p53-MDM2 interaction inhibitor.
价 格:¥电议型 号:T5555产 地:中国大陆
-
T5144Desmopressin acetate (16679-58-6 free base);醋酸去氨加压素Desmopressin acetate|||DDAVP;Desmopressin acetate
Desmopressin acetate (16679-58-6 free base) (DDAVP) is the synthetic analog of the antidiuretic hormone arginine vasopressin. Vasopressin Receptor The antidiuretic properties of desmopressin have led to its use in polyuric conditions including primary nocturnal enuresis, nocturia, and diabetes insipidus. Desmopressin acetate (16679-58-6 free base) works by limiting the amount of water that is eliminated in the urine. Desmopressin acetate (16679-58-6 free base) binds to V2 receptors in renal coll
价 格:¥电议型 号:T5144产 地:中国大陆
-
T5049NVP-BSK805化合物NVP-BSK805NVP-BSK805 2HCl|||8-[3,5-二氟-4-(4-吗啉基甲基)苯基]-2-[1-(4-哌啶基)-1H-吡唑-4-基]喹喔啉|||BSK 8
NVP-BSK805 (BSK 805) is an ATP-competitive JAK2 inhibitor.
价 格:¥电议型 号:T5049产 地:中国大陆
-
T4536Pleconaril;普可那利VP 63843|||Win 63843|||Picovir;VP 63843|||Win 63843|||Picovir|||普可那利
Pleconaril (VP 63843) is a capsid inhibitor used previously to treat enterovirus infections. Pleconaril is effective in inhibiting replication (IC50: 50 nM).
价 格:¥电议型 号:T4536产 地:中国大陆
-
T4220BQR-695;化合物BQR695BQR695|||NVP-BQR695;BQR695|||NVP-BQR695
BQR-695 (NVP-BQR695) is a phosphatidylinositol 4-kinase (PI4K) inhibitor with IC50s of 80 and 3.5 nM for human PI4KIIIβ and Plasmodium variant of PI4KIIIβ, respectively.
价 格:¥电议型 号:T4220产 地:中国大陆
-
T41002HCVP-IN-1;HCVP-IN-1HCVP-IN-1
HCVP-IN-1 (compound 1) is a hepatitis C viral polymerase (HCVP) inhibitor.
价 格:¥电议型 号:T41002产 地:中国大陆
-
T40884SKF 100398;SKF 100398d(CH2)5Tyr(Et)VAVP;d(CH2)5Tyr(Et)VAVP
SKF 100398, also known as d(CH2)5Tyr(Et)VAVP, is a particular analog of arginine vasopressin (AVP). It acts as a specific antagonist, specifically targeting the antidiuretic effect caused by both exogenous and endogenous AVP.
价 格:¥电议型 号:T40884产 地:中国大陆