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：3530375
自主品牌
已选条件
-
TMA1603Parishin CParishin C,Inhibitor,inhibit
Parishin C is a phenolic glycoside and a major component of G. elata, have antioxidant property
价 格：￥电议型 号：TMA1603产 地：中国大陆
-
T60061RU-TRAAK-2RU TRAAK 2,inhibit,Inhibitor,channels,reversible,TRAAK non-K2P,Potassium Channel,RUTRAAK2,
RU-TRAAK-2 is a reversible inhibitor of TWIK-related arachidonic acid-stimulated K+ channel with no activity for non-K2P channels including Kv1.2, GIRK2, and Slo1.
价 格：￥电议型 号：T60061产 地：中国大陆
-
T60167Eubulus-A80EubulusA80
Eubulus-A80 is a anti-tumor agent (WO2021/183702, Compound A80).
价 格：￥电议型 号：T60167产 地：中国大陆
-
T9602MonocaprinMonocaprin
Monocaprin is a 1-monoglyceride of capric acid that has antimicrobial activity against enveloped viruses, certain bacteria, and the yeast Candida albicans.
价 格：￥电议型 号：T9602产 地：中国大陆
-
T6607Nitenpyraminhibit,nAChR,Inhibitor,Nicotinic acetylcholine receptors,Nitenpyram
Nitenpyram is a nicotinic acetylcholine receptor (AchR) agonist, used as veterinary medicine to treat parasites of livestock and pets.
价 格：￥电议型 号：T6607产 地：中国大陆
-
T60009YS-370YS370,YS 370
YS-370 is an orally active inhibitor of P-gp and shows moderate inhibition against CYP3A4. YS-370 effectively reverses multidrug resistance to paclitaxel and colchicine and exhibits stronger antitumor activity in combination with paclitaxel.
价 格：￥电议型 号：T60009产 地：中国大陆
-
T6929Pantoprazole sodiumstability,inhibit,anti-secretory,SKF 96022,Pantoprazole sodium,SKF96022,H+/K+-ATP
Pantoprazole Sodium is the sodium salt form of a substituted benzimidazole with proton pump inhibitor activity. Pantoprazole is a lipophilic, weak base that crosses the parietal cell membrane and enters the acidic parietal cell canaliculus where it becomes protonated, producing the active metabolite sulfenamide, which forms an irreversible covalent bond with two sites of the H+/K+-ATPase enzyme located on the gastric parietal cell, thereby inhibiting both basal and stimulated gastric acid produc
价 格：￥电议型 号：T6929产 地：中国大陆
-
T60063WAY-323975
WAY-323975 is a nonfluorescent inhibitors of Fluorogen–Fluorogen Activating Protein Binding Pairn.
价 格：￥电议型 号：T60063产 地：中国大陆
-
T206083-Benzoylpyridine
3-Benzoylpyridine is a decomposition product of HGG-12 which is the soman antidote.
价 格：￥电议型 号：T20608产 地：中国大陆
-
T60681DS12881479
DS12881479 can be used in cancer research which is a potent and selective inhibitor of Mnk1(IC 50 =21 nM) [1].
价 格：￥电议型 号：T60681产 地：中国大陆
-
T38345SQ609SQ609,SQ-609
SQ609 is a potential anti-tuberculosis drug selected from a library of dipiperidine derivatives. SQ609 showed significant anti-tuberculous activity in mouse macrophages in vitro[1].
价 格：￥电议型 号：T38345产 地：中国大陆
-
T60161CP-289CP289
CP-289 is a potent C5a receptor antagonist with IC50 of 1 μM.
价 格：￥电议型 号：T60161产 地：中国大陆
-
TN12603-O-beta-D-GlucopyranosylplatycodigeninInhibitor,3 O beta D Glucopyranosylplatycodigenin,inhibit,3Ob
3-O-beta-D-Glucopyranosylplatycodigenin is isolated from the roots of Platycodon grandiflorum.
价 格：￥电议型 号：TN1260产 地：中国大陆
-
T21747VU0483605Inhibitor,inhibit,VU0483605,Metabotropic glutamate receptors,allosteric modulator,brain pen
VU0483605 is an effective and selective positive allosteric modulator of mGluR1 with EC50s of 390 and 356 nM for human and rat, respectively.
价 格：￥电议型 号：T21747产 地：中国大陆
-
T6606NicaravenNicaraven,Inhibitor,inhibit
Nicaraven, a hydroxyl radical scavenger, has neuroprotective and antivasospastic effects.
价 格：￥电议型 号：T6606产 地：中国大陆
-
TP1604LThioredoxin reductase peptide acetateThioredoxin reductase peptide acetate
Thioredoxin reductase peptide acetate corresponds to residues 53–67 in thioredoxin reductase (TrxR), used in thioredoxin reductase research.Mammalian thioredoxin reductase (TR) catalyzes the reduction of the redox-active disulfide bond of thioredoxin (Trx) and is similar in structure and mechanism to glutathione reductase except for a C-terminal 16-amino acid extension containing a rare vicinal selenylsulfide bond.
价 格：￥电议型 号：TP1604L产 地：中国大陆
-
T6086Clopamidecardiac,diuretic,Na+ channels,Na channels,inhibit,Sodium Channel,Clopamide,thiazide-like,an
Clopamide is a piperidine and sulfamoylbenzamide-based diuretic with thiazide-like diuretic activity.
价 格：￥电议型 号：T6086产 地：中国大陆
-
TP1696LCGGRGD acetate(1260223-44-6 free base)CGGRGD acetate(1260223446 free base),CGGRGD acetate(1260223 44
CGGRGD acetate is a RGD derivative with cysteine as the n-terminal. CGGRGD was synthesized by solid phase peptide synthesis technology, and amino2-cyanobenzothiazole (2-cyanobenzothiazole) (2-cyanobenzothiazole (CBT) was added on the surface of PCL fiber for ammoniation.
价 格：￥电议型 号：TP1696L产 地：中国大陆
-
T16040Mepazinediffuse,B cell,inhibit,large,mucosa associated lymphoid tissue lymphoma translocation gene 1
Mepazine is a potent and selective inhibitor of MALT1. Mepazine inhibits GSTMALT1 full length and GSTMALT1 325-760 with IC50s of 0.83 μM and 0.42 μM. Mepazine enhances apoptosis and affects the cell viability.
价 格：￥电议型 号：T16040产 地：中国大陆
-
T60160STX-0119STX0119
STX-0119 is a selective, orally active STAT3 dimerization inhibitor. STX-0119 inhibits STAT3 transcription with an IC50 of 74 μM.
价 格：￥电议型 号：T60160产 地：中国大陆
