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：3476101
自主品牌
已选条件
-
TN1012LFebrifugine dihydrochlorideInhibitor,Parasite,Febrifugine dihydrochloride,antimalarial,alkaloid,Quin
Febrifugine dihydrochloride is a biochemical with therapeutic activity regarding malaria, cancer, fibrosis and inflammatory diseases.
价 格：￥电议型 号：TN1012L产 地：中国大陆
-
T14362LAY 9944 dihydrochloride1(2chlorophenyl)N[[4[(2chlorophenyl)methylaminomethyl]cyclohexyl]methyl]metha
AY 9944 dihydrochloride is a intermediate.
价 格：￥电议型 号：T14362L产 地：中国大陆
-
T9084Cetirizine Impurity B dihydrochlorideinhibit,Cetirizine Impurity B,Inhibitor,Cetirizine Impurity B d
Cetirizine Impurity B dihydrochloride is an impurity of Cetirizine dihydrochloride. Cetirizine is a second-generation antihistamine. Cetirizine is a specific, orally active and long-acting histamine H1-receptor antagonist. Cetirizine marks antiallergic properties and inhibits eosinophil chemotaxis during the allergic response.
价 格：￥电议型 号：T9084产 地：中国大陆
-
T32613LCB 03-0110 dihydrochlorideLCB 030110 dihydrochloride,LCB 03 0110 dihydrochloride
LCB 03-0110 Dihydrochloride is a potent inhibitor of the c-Src kinase (IC50 = 1.3 nM) and tyrosine kinases in the BTK and SYK family, as well as in the DDR2 family. It inhibits LPS-induced activation of macrophages and TGF-β1-induced activation of fibroblasts in vitro, inhibits activation of macrophages and fibroblasts, and inhibits scarring in wound healing models.
价 格：￥电议型 号：T32613产 地：中国大陆
-
T6571Lomerizine dihydrochlorideCa2+ channels,Ca channels,inhibit,Lomerizine,KB 2796,KB2796,Lomerizine dih
Lomerizine dihydrochloride is an antagonist of L- and T-type voltage-gated calcium channels used to treat migraine.
价 格：￥电议型 号：T6571产 地：中国大陆
-
T6951Pramipexole dihydrochloride hydratetransient,Pramipexole dihydrochloride,Pramipexole dihydrochloride
Pramipexole Dihydrochloride is the hydrochloride salt of pramipexole, a benzothiazole derivative. As a nonergot dopamine agonist, pramipexole binds to D2 and D3 dopamine receptors in the striatum and substantia nigra of the brain.
价 格：￥电议型 号：T6951产 地：中国大陆
-
T35341NVP-BSK805 dihydrochloride
NVP-BSK805 dihydrochloride is an effective and selective inhibitor of JAK2 with IC50s of 0.5 nM, 10.76 nM, 18.68 nM, and 31.63 nM for JAK2, TYK2, JAK3, and JAK1.
价 格：￥电议型 号：T35341产 地：中国大陆
-
T7117Sapropterin dihydrochloride(6R)-BH4,Sapropterin,Inhibitor,inhibit,Sapropterin dihydrochloride
Sapropterin dihydrochloride is phenylalanine hydroxylase agonist that is approved for the treatment of BH4 responsive PKU.
价 格：￥电议型 号：T7117产 地：中国大陆
-
T13890SMARCA-BD ligand 1 for Protac dihydrochlorideSMARCABD ligand 1 for Protac dihydrochloride,SMARCA BD
SMARCA-BD ligand 1 for Protac dihydrochloride binds to the BAF ATPase subunits SMARCA2, and used for degrading SMARCA2, based on PROTAC.
价 格：￥电议型 号：T13890产 地：中国大陆
-
T10837Clocapramine dihydrochloride hydrateClocapramine dihydrochloride hydrate
Clocapramine dihydrochloride hydrate is an antagonist of the 5-HT2A and D2 receptors.
价 格：￥电议型 号：T10837产 地：中国大陆
-
T7195GSK369796 Dihydrochlorideinhibit,GSK 369796,GSK369796,Inhibitor,GSK369796 Dihydrochloride,GSK-369796
GSK369796 Dihydrochloride,is an anti-malaria drug candidate. is an affordable and effective antimalarial and inhibits hERG potassium ion channel repolarization(IC50 of 7.5 μM)
价 格：￥电议型 号：T7195产 地：中国大陆
-
T23007MM 77 dihydrochloride
MM 77 dihydrochloride is an effecitve 5-HT1A receptor postsynaptic antagonist with anxiolytic-like activity.
价 格：￥电议型 号：T23007产 地：中国大陆
-
T7501Iso-H7 dihydrochlorideIso H7 dihydrochloride,Iso-H-7 dihydrochloride,IsoH7 dihydrochloride
Iso-H7 dihydrochloride is a less potent inhibitor of phosphokinase C than H-7.
价 格：￥电议型 号：T7501产 地：中国大陆
-
T602484-Aminobenzamidine dihydrochloride
4-Aminobenzamidine (p-Aminobenzamidine) dihydrochloride is a strong trypsin inhibitor and a relatively weak inhibitor of urokinase type plasminogen activator (uPA) (K i =82 μM). 4-Aminobenzamidine can inhibit growth of a human prostate tumor in SCID mice [1] [2].
价 格：￥电议型 号：T60248产 地：中国大陆
-
TQ0133Amifostine thiol dihydrochlorideWR1065,Amifostine thiol dihydrochloride,Inhibitor,MDM-2/p53,WR-1065,
WR-1065 dihydrochloride can activate p53 through a JNK-dependent signaling pathway. It also protects normal tissues from the toxic effects of certain cancer drugs.
价 格：￥电议型 号：TQ0133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
-
T36994MRT 67307 dihydrochlorideMRT 67307 dihydrochloride
MRT 67307 dihydrochloride is a dual inhibitor of the IKKε and TBK-1 with IC50s of 160 and 19 nM, respectively. MRT67307 dihydrochloride also inhibits ULK1 and ULK2 with IC50s of 45 and 38 nM, respectively. MRT67307 dihydrochloride also blocks autophagy in cells.
价 格：￥电议型 号：T36994产 地：中国大陆
-
T35528LTD52 dihydrochloride
TD52 dihydrochloride, an Erlotinib derivative, is an orally active, potent cancerous inhibitor of protein phosphatase 2A (CIP2A) inhibitor. TD52 dihydrochloride mediates the apoptotic effect in triple-negative breast cancer (TNBC) cells via regulating the CIP2A/PP2A/p-Akt signalling pathway. TD52 dihydrochloride indirectly reduced CIP2A by disturbing Elk1 binding to the CIP2A promoter. TD52 dihydrochloride has less p-EGFR inhibition and has potent anti-cancer activity.
价 格：￥电议型 号：T35528L产 地：中国大陆
-
T9172Simufilam dihydrochlorideInhibitor,PTI-125,Simufilam,inhibit,PTI 125,PTI125,Simufilam dihydrochlorid
Simufilam dihydrochloride is a low toxicity, orally active filamin A (FLNA) activator, which can be used for the research of Alzheimer´s disease. Simufilam dihydrochloride preferentially binds altered FLNA and restores its native conformation, restoring receptor and synaptic activities and reducing its α7nAChR/TLR4 associations and downstream pathologies.
价 格：￥电议型 号：T9172产 地：中国大陆
-
T8822JNJ-5207852 dihydrochlorideInhibitor,toxicity,JNJ5207852,inhibit,low,JNJ 5207852,sleep,REM,JNJ-52078
JNJ-5207852 is a novel, non-imidazole histamine H3 receptor antagonist, with high affinity at the rat (pKi=8.9) and human (pKi=9.24) H3 receptor.
价 格：￥电议型 号：T8822产 地：中国大陆
