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：3296776
自主品牌
已选条件
-
T24814Sortin2；化合物 T24814Sortin-2|||Sortin 2；Sortin-2|||Sortin 2
Sortin2 is a sorting inhibitor that acts upstream from the morphological marker of lateral root primordium formation, the mitotic activity.
价 格：￥电议型 号：T24814产 地：中国大陆
-
T24730Roslin 2 bromide；化合物Roslin 2 bromideRoslin-2|||Benzylhexamethylenetetramine bromide|||Roslin2；Roslin
Roslin 2 bromide (Benzylhexamethylenetetramine bromide) is a p53 reactivator that disrupts the binding of FAK and p5. Roslin 2 bromide exhibits anticancer effects.
价 格：￥电议型 号：T24730产 地：中国大陆
-
T24683Pterophyllin 2；化合物 T24683Pterophyllin-2|||Pterophyllin2；Pterophyllin-2|||Pterophyllin2
Pterophyllin 2 is an agent of natural antifungal. It also against postharvest fruit pathogenic fungi.
价 格：￥电议型 号：T24683产 地：中国大陆
-
T24539nNOS-IN-25；化合物 T24539nNOS inhibitor 25|||nNOS inhibitor-25|||nNOSIN25；nNOS inhibitor 25|||nNOS inhib
nNOS-IN-25 is an effective, selective, and cell-permeable inhibitor of neuronal nitric oxide synthase.
价 格：￥电议型 号：T24539产 地：中国大陆
-
T24439MDK6204；化合物 T24439CLK1/2 IN 2|||CLK1/2IN2|||CLK1/2-inhibitor-2|||CLK1/2-IN-2|||CLK1/2 inhibitor 2；CL
MDK6204 is a selective inhibitor of CLK1 and CLK2.
价 格：￥电议型 号：T24439产 地：中国大陆
-
T24436Mcl1-IN-26；化合物 T24436Mcl1-IN-26
Mcl1-IN-26 is an effective and selective myeloid cell leukemia 1 inhibitor.
价 格：￥电议型 号：T24436产 地：中国大陆
-
T24410LIMK-IN-22j；化合物LIMK-IN-22jLIMK IN 22j|||LIMK inhibitor-22j|||LIMK inhibitor 22j；LIMK IN 22j|||LIMK i
LIMK-IN-22j (LIMK inhibitor 22j) is an effective and selective inhibitor of LIMK.
价 格：￥电议型 号：T24410产 地：中国大陆
-
T24396LDN-209929；化合物 T24396LDN-209929 dihydrochloride|||LDN209929 dihydrochloride|||LDN 209929 dihydrochlo
LDN-209929 2HCl is a potent and selective inhibitor of haspin kinase.
价 格：￥电议型 号：T24396产 地：中国大陆
-
T2438HMN-214；化合物HMN214IVX-214|||HMN214；IVX-214|||HMN214
HMN-214 (IVX-214) is a potent PLK1 inhibitor with an average IC50 of 0.12 μM.
价 格：￥电议型 号：T2438产 地：中国大陆
-
T24133HDAC8-IN-20a；化合物HDAC8-IN-20aHDAC8 IN 20a|||HDAC8IN20a|||HDAC8 inhibitor-20a|||HDAC8 inhibitor 20a；HD
HDAC8-IN-20a (HDAC8 inhibitor-20a) is a potent and selective HDAC8 inhibitor with an IC50 of 27 nM. HDAC8-IN-20a blocks activation of growth receptor survival signals.
价 格：￥电议型 号：T24133产 地：中国大陆
-
T24073PTP1B-IN-4；化合物PTP1B-IN-4NUN 17724|||PTP1B-inhibitor-2|||PTP1B IN 2|||PTP1B-IN-2|||PTP1B-inhibitor-4|
PTP1B-IN-4 (NUN-17724) is an allosteric PTP1B inhibitor with an IC50 of 8 μM. PTP1B-IN-4 can be used in studies about obesity and diabetes.
价 格：￥电议型 号：T24073产 地：中国大陆
-
T23923Cyclobutyrol；化合物 T23923BRN 2209058|||BRN-2209058|||BRN2209058|||Cyclobutyrolum|||JL 130；BRN 2209058|
Cyclobutyrol is a choleretic agent. It also inhibits biliary lipid secretion.
价 格：￥电议型 号：T23923产 地：中国大陆
-
T23868Ceefourin-2；化合物 T23868Ceefourin2|||Ceefourin 2；Ceefourin2|||Ceefourin 2
Ceefourin-2 is a highly selective multidrug resistance protein 4 inhibitor.
价 格：￥电议型 号：T23868产 地：中国大陆
-
T23667AGN-201904；化合物 AGN-201904AGN201904|||AGN 201904；AGN201904|||AGN 201904
AGN-201904 is a proton pump inhibitor, an omeprazole prodrug, which delays aging and may be used for the prevention and treatment of peptic ulcers.
价 格：￥电议型 号：T23667产 地：中国大陆
-
T23046N-tert-butyl-α-Phenylnitrone；N-叔丁基-α-苯基硝酮(Z)-N-benzylidene-2-Methylpropan-2-aMine oxide；(Z)-N-benzyl
N-tert-butyl-α-Phenylnitrone ((Z)-N-benzylidene-2-Methylpropan-2-aMine oxide) inhibits COX2 catalytic activity. N-tert-butyl-α-Phenylnitrone((Z)-N-benzylidene-2-Methylpropan-2-aMine oxide) possesses potent reactive oxygen species scavenging, anti-inflammatory, neuroprotective, anti-aging, and anti-diabetic activities, and can penetrate the blood-brain barrier.
价 格：￥电议型 号：T23046产 地：中国大陆
-
T22817GSK 789472 hydrochloride；GSK 789472盐酸盐GSK-789472 HCl|||1-phenyl-3-(piperidin-2-ylmethyl)imidazolidin
GSK 789472 hydrochloride is both a dopamine D3 receptor antagonist and a D2 partial agonist.
价 格：￥电议型 号：T22817产 地：中国大陆
-
T2265Bimiralisib；化合物PI3K-IN-25-(4,6-dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine||
Bimiralisib (PI3K-IN-2) is an orally bioavailable pan inhibitor of PI3K and inhibitor of the mTOR, with potential antineoplastic activity. PI3K-IN-2 inhibits the PI3K kinase isoforms alpha, beta, gamma and delta and, to a lesser extent, mTOR kinase, which may result in tumor cell apoptosis and growth inhibition in cells overexpressing PI3K/mTOR. Activation of the PI3K/mTOR pathway promotes cell growth, survival, and resistance to both chemotherapy and radiotherapy.
价 格：￥电议型 号：T2265产 地：中国大陆
-
T22491PDE7-IN-2；化合物 PDE7-IN-2PDE7-IN-2
PDE7-IN-2 is an inhibitor of phosphodiesterase 7 (IC50 = 2.1 ?M) and can be used in Parkinson´s disease studies.
价 格：￥电议型 号：T22491产 地：中国大陆
-
T22432SU5208；化合物SU52083-[(Thien-2-yl)methylene]-2-indolinone；3-[(Thien-2-yl)methylene]-2-indolinone
SU5208 (3-[(Thien-2-yl)methylene]-2-indolinone) is a compound with bioactivity.SU5208 inhibits vascular endothelial growth factor receptor-2 (VEGFR2).
价 格：￥电议型 号：T22432产 地：中国大陆
-
T22256c-Kit-IN-5-1；化合物AMG-253-(2-Aminoquinazolin-6-yl)-4-methyl-1-(4-(oxazol-2-yl)phenyl)pyridin-2(1H)-one
c-Kit-IN-5-1 (AMG-25) is a novel selective and potent c-Kit inhibitor.
价 格：￥电议型 号：T22256产 地：中国大陆
