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：3809804
自主品牌
已选条件
-
T70818TC-2153；化合物 TC-2153 HClTC-2153
TC-2153 is a selective inhibitor of striatal-enriched protein tyrosine phosphatase (STEP), exhibiting psychotropic activity and low acute toxicity. This compound not only enhances the expression of brain-derived neurotropic factor (BDNF) in the brain but also reduces the mRNA levels of MAOA and 5-HT1A receptors in the midbrain. Additionally, TC-2153 inhibits 5-HT2A receptor-mediated signaling.
价 格：￥电议型 号：T70818产 地：中国大陆
-
T70153Pipoxolan hydrochloride；化合物 Pipoxolan hydrochloridePipoxolan hydrochloride
Pipoxolan (HCl) is an antispasmodic drug. In vivo, the drug inhibited the contractions of intestines caused by neostigmine, barium chloride or injection of acetylcholine. The drug possesses ganglioplegic action and inhibited the decrease in blood pressure caused by stimulation of the vagus nerve. The drug is marketed under tradename Rowapraxin worldwide for the treatment of spasms and colics in the gastrointestinal tract, gallbladder and urogenital area, bronchial spasms, spastic menstrual cramp
价 格：￥电议型 号：T70153产 地：中国大陆
-
T6S1538Neochlorogenic acid；新绿原酸trans-5-O-Caffeoylquinic acid|||Neochlorogenate|||5-O-Caffeoylquinic acid；新绿
Neochlorogenic acid (trans-5-O-Caffeoylquinic acid) is an antioxidant compound used in the treatment of oxidative stress and related afflictions.
价 格：￥电议型 号：T6S1538产 地：中国大陆
-
T6S1537Cryptochlorogenic acid；隐绿原酸4-O-Caffeoylquinic acid|||4-Caffeoylquinic acid；隐绿原酸|||4-O-Caffeoylquinic
1. Cryptochlorogenic acid (4-O-Caffeoylquinic acid) has antioxidant activity.
价 格：￥电议型 号：T6S1537产 地：中国大陆
-
T6933Peficitinib；化合物PeficitinibASP015K|||JNJ-54781532；ASP015K|||JNJ-54781532
Peficitinib (ASP015K) (ASP015K, JNJ-54781532) is an orally bioavailable JAK inhibitor. Phase 3.
价 格：￥电议型 号：T6933产 地：中国大陆
-
T69153T0510-3657；化合物 T0510-3657T0510-3657
T0510-3657 is a selective activator of GPR17, inhibiting cAMP levels, with potential for playing a key role in the development of a treatment against diseases such as, multiple sclerosis, Parkinson disease, Alzheimer´s disease, and cancer.
价 格：￥电议型 号：T69153产 地：中国大陆
-
T69055PD153035 nitrate；化合物 PD153035 nitratePD153035 nitrate
PD153035 is a ATP-competitive EGFR inhibitor with an IC50 and Ki of 25 and 6 pM. PD153035 effectively blocks the enhancement of mitogenesis, induction of early gene expression, and oncogenic transformation that occur in response to EGF receptor stimulation. With human fibroblasts and epidermoid carcinoma cells, PD153035 at nanomolar concentrations rapidly inhibits EGFR autophosphorylation. With breast and ovarian cancer cells, PD153035 not only blocks cell growth via inhibition of EGFR, but also
价 格：￥电议型 号：T69055产 地：中国大陆
-
T68911LAF-153；化合物 LAF-153LAF-153
LAF-153 is a reversible Methionine Aminopeptidase?2 (MetAP-2) Inhibitor.
价 格：￥电议型 号：T68911产 地：中国大陆
-
T68698VPC 23153；化合物 VPC 23153VPC 23153
VPC 23153 is a sphingosine 1-phosphate 4 receptor agonist. This hygroscopic phospholipid causes contraction of pulmonary artries in rats.
价 格：￥电议型 号：T68698产 地：中国大陆
-
T68475AO-1535；化合物 AO-1535AO-1535
AO-1535 is a semisynthetic monoglycosylceramide derived from O-glycosilated sphingosine. It has been shown to inhibit superoxide production by macrophages suggesting a potential clinical application of AO 1535 in the treatment of inflammatory dermatoses.
价 格：￥电议型 号：T68475产 地：中国大陆
-
T68153Tazomeline；他唑美林Tazomeline
Tazomeline is a muscarinic M1 receptor agonist with neuroprotective activity.
价 格：￥电议型 号：T68153产 地：中国大陆
-
T68151LTallimustine HCl；他莫司汀盐酸盐Tallimustine HCl(115308-98-0 Free base)；Tallimustine HCl(115308-98-0 Free ba
Tallimustine HCl is a DNA inhibitor, an AT-specific alkylated antitumor derivative of diamycin.Tallimustine HCl can be used in severe combined immunodeficiency mouse models of adult myelogenous leukemia, which can be used for the treatment of leukemia.
价 格：￥电议型 号：T68151L产 地：中国大陆
-
T68051LRS 15385-198；化合物RS 15385-198RS 15385-198
RS 15385-198 is a less active isomer of Delequamine. Delequamine is a selective alpha2-adrenergic receptor antagonist.
价 格：￥电议型 号：T68051L产 地：中国大陆
-
T68051Delequamine；地来夸明RS 15385-197；RS 15385-197
Delequamine (RS 15385-197) is a selective and potent TNIK inhibitor (IC50: 8 nM).TINK-IN-1 inhibits colorectal cancer cell viability and can be used to study mental retardation.
价 格：￥电议型 号：T68051产 地：中国大陆
-
T6718Zingerone；姜酮Gingerone|||Vanillylacetone|||NSC 15335；Gingerone|||Vanillylacetone|||姜酮|||NSC 15335
Zingerone (Vanillylacetone) is a nontoxic methoxyphenol isolated from Zingiber officinale, with potent anti-inflammatory, antidiabetic, antidiarrhoeic, antilipolytic, antispasmodic and anti-tumor properties. Zingerone(Gingerone) alleviates oxidative stress and inflammation, down-regulates NF-κB mediated signaling pathways. Zingerone(Gingerone) acts as an anti-mitotic agent, and inhibits the growth of neuroblastoma cells.
价 格：￥电议型 号：T6718产 地：中国大陆
-
T67153N1,N2-Dimethylphthalamide；化合物 N1,N2-DimethylphthalamideN1,N2-Dimethylphthalamide
N1,N2-Dimethylphthalamide is a useful organic compound for research related to life sciences. The catalog number is T67153 and the CAS number is 19532-98-0.
价 格：￥电议型 号：T67153产 地：中国大陆
-
T66153Boc-D-Tyr-OH；化合物 Boc-D-Tyr-OHBoc-D-Tyr-OH
Boc-D-Tyr-OH is a useful organic compound for research related to life sciences. The catalog number is T66153 and the CAS number is 70642-86-3.
价 格：￥电议型 号：T66153产 地：中国大陆
-
T65153Ethyl 4,4,4-trifluorocrotonate；化合物 Ethyl 4,4,4-trifluorocrotonateEthyl 4,4,4-trifluorocrotonate
Ethyl 4,4,4-trifluorocrotonate is a useful organic compound for research related to life sciences and the catalog number is T65153.
价 格：￥电议型 号：T65153产 地：中国大陆
-
T64153Glyoxalase I inhibitor 1；化合物 Glyoxalase I inhibitor 1Glyoxalase I inhibitor 1
Glyoxalase I inhibitor 1 is a potent inhibitor of glyoxalase I (GLO1) (IC50: 26 nM).
价 格：￥电议型 号：T64153产 地：中国大陆
-
T64101FTI-2153 TFA；化合物 FTI-2153 TFAFTI-2153 TFA
FTI-2153 TFA is a highly selective and potent inhibitor of the farnesyltransferase (FTase) enzyme (IC50: 1.4 nM). The inhibition activity was more than 3000 times that of Rap1A protein processing.
价 格：￥电议型 号：T64101产 地：中国大陆
