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TP1579Angiotensin I/II (1-6)Angiotensin I/II (16),Angiotensin I/II (1-6),Inhibitor,inhibit,Angiotensin I/I
Angiotensin I/II (1-6) is a peptide (ASP-ARG-VAL-TYR-ILE-HIS) that contains the amino acids 1-6 and is converted from Angiotensin I/II peptide.
价 格：￥电议型 号：TP1579产 地：中国大陆
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T39291GilmelisibGilmelisib
Gilmelisib is an antineoplastic. Gilmelisib is a PI3K inhibitor ( IC 50 <1 nM for PI3K p110α) extracted from WO2017101847 A1, compound 1.
价 格：￥电议型 号：T39291产 地：中国大陆
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T87944-MMPBLOX,4 MMPB,radical,Inhibitor,inhibit,4-MMPB,scavenging,Lipoxygenase,cancer,Apoptosis,4MMPB,inh
15-Lipoxygenase Inhibitor 1 is a selective inhibitor of 15-lipoxygenase, with an IC50 of 18 μM. 4-MMPB has IC50s of 19.5 μM and 19.1 μM for soybean 15-lipoxygenase (SLO) and human 15-lipoxygenase-1 (15-LOX-1), respectively. 4-MMPB has potential for the research of prostate cancer.
价 格：￥电议型 号：T8794产 地：中国大陆
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T6647Rotigotine-Rotigotine,dopamine,5-HT1A,Adrenergic Receptor,receptor,N0923,Serotonin Receptor,N 0923,5
Rotigotine is a non-ergot dopamine receptor agonist used in the therapy of Parkinson disease and restless leg syndrome. Administered as a once-daily transdermal patch, Rotigotine has not been associated with serum enzyme elevations during treatment or with episodes of clinically apparent liver injury.
价 格：￥电议型 号：T6647产 地：中国大陆
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T6S1487Ginsenoside Rg5Nuclear factor-κB,Inhibitor,Ginsenoside Rg5,Cyclooxygenase,Ginsenoside Rg 5,NF-κB,COX
1. Ginsenoside Rg5 could be a beneficial agent for the treatment of Alzheimer´s disease. 2. Ginsenoside Rg5 suppresses LPS-induced nitric oxide (NO) production and proinflammatory TNF-α secretion. 3. Ginsenoside Rg5 can ameliorate lung inflammation possibly by inhibiting the binding of LPS to toll-like receptor (TLR)-4 on macrophages. 4. Ginsenoside Rg5 plays a novel role as an IGF-1R agonist, promoting therapeutic angiogenesis and improving hypertension without adverse effects in the vasc
价 格：￥电议型 号：T6S1487产 地：中国大陆
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T6S20258-?O-?Acetylharpagideinhibit,Bacterial,8?O?Acetylharpagide,Inhibitor,8 ?O ?Acetylharpagide
1. 8-O-Acetylharpagide has anti-inflammatory activity. 2. 8-O-Acetylharpagide has antibacteria and antiviral activities. 3. 8-O-Acetylharpagide has a biological activity on isolated smooth muscle preparations from guinea pig.
价 格：￥电议型 号：T6S2025产 地：中国大陆
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TN1096Ginsenoside Ra1Ginsenoside Ra1,inhibit,Inhibitor,Ginsenoside Ra 1,Ginsenoside Ra-1
Ginsenoside Ra1 is a component from ginseng. Ginsenoside Ra1 shows significant inhibitory effects on protein tyrosine kinase (PTK) activation induced by hypoxia/reoxygenation (H/R).
价 格：￥电议型 号：TN1096产 地：中国大陆
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TP1528Angiotensin I/II (1-5)Angiotensin I/II (15),inhibit,Angiotensin Receptor,Inhibitor,Angiotensin I/II
Angiotensin I/II (1-5) is a peptide (ASP-ARG-VAL-TYR-ILE) that contains the amino acids 1-5 and is converted from Angiotensin I/II.
价 格：￥电议型 号：TP1528产 地：中国大陆
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T8157CenthaquinPMZ2010,inhibit,systemic vascular resistance,Inhibitor,Centhaquin,haemorrhagic shock,PMZ 2
Centhaquine is an adrenergic receptor potentially for the treatment of postoperative pain and for the resuscitation of hypovolemic shock
价 格：￥电议型 号：T8157产 地：中国大陆
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T8322BL-918inhibit,disease,BL-918,cytoprotective,BL 918,BL918,Autophagy,kinase,autophagic,Unc-51 like kin
BL-918 is a potent activator of UNC-51-like kinase 1 (ULK1) with an EC50 of 24.14 nM.
价 格：￥电议型 号：T8322产 地：中国大陆
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T7164Levalbuterol tartrateinhibit,Beta Receptor,Adrenergic Receptor,Levosalbutamol,Levalbuterol,Levalbute
Levosalbutamol tartrate is the β2-adrenergic receptor agonist,and is used to treatment of asthma.
价 格：￥电议型 号：T7164产 地：中国大陆
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T64377AGI-41998 tautomers8(4bromophenyl)6(4methoxyphenyl)2((2,2,2trifluoroethyl)imino)2,6dihydropyrido[4,3
AGI-41998 tautomers is a tautomerism of pyrido[4,3-d]pyrimidin-7(6H)-one, 8-(4-bromophenyl)-6-(4-methoxyphenyl)-2-[(2,2,2-trifluoroethyl)amino]-. pyrido[4,3-d]pyrimidin-7(6H)-one, 8-(4-bromophenyl)-6-(4-methoxyphenyl)-2-[(2,2,2-trifluoroethyl)amino]- is a S-adenosylmethionine synthase isoform type-2 inhibitor, IC50= 0.022μM.
价 格：￥电议型 号：T64377产 地：中国大陆
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T7577Angiotensin III, human, mouseAngiotensin Receptor,Inhibitor,Angiotensin III, human, mouse,inhibit
Angiotensin III, human, mouse(3TFA) is an endogenous angiotensin II receptor (AT2R) agonist(IC50s of 0.648 nM).
价 格：￥电议型 号：T7577产 地：中国大陆
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T6856Halofuginoneosteoarthritis,collagen-1,Na+ channels,Calcium Channel,Na channels,Transforming growth f
Halofuginone, the competitive inhibitor of prolyl-tRNA synthetase（Ki=18.3 nM）, could also down-regulate Smad3 and blocked TGF-β signaling at 10 ng/ml in the mammal.
价 格：￥电议型 号：T6856产 地：中国大陆
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T6514GlasdegibInhibitor,PF 04449913,Glasdegib,inhibit,Smoothened,Smo,PF04449913
Glasdegib (PF-04449913) is a potent, and orally bioavailable Smoothened (Smo) inhibitor with IC50 of 5 nM. Phase 2.
价 格：￥电议型 号：T6514产 地：中国大陆
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T6779BEC hydrochlorideInhibitor,NF-κB,hyperresponsiveness,metaplasia,inhibit,Arginase,BEC,BEC hydrochlori
BEC HCl is a competitive arginase inhibitor, which bind slowly. Ki of BEC HCl is 0.31 μM (pH7.5) for Arginase II, and is 0.4-0.6 μM for rat Arginase I.
价 格：￥电议型 号：T6779产 地：中国大陆
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T8533ML318acyl-binding,pyoverdine,Antibiotic,production,ML318,PAO1,ML-318,Inhibitor,ML 318,iron,P.aerugin
ML318 is a biaryl nitrile PvdQ acylase inhibitor (IC50 of 20 nM for binding in the acyl-binding site). ML318 inhibits P. aeruginosa (PAO1) with IC50 of 19 μM. ML318 prevents pyoverdine production and limits the growth of P. aeruginosa under iron-limiting conditions.
价 格：￥电议型 号：T8533产 地：中国大陆
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T9575MRTX9768SDMA,toxicity,glioblastoma,orally,MRTX9768,low,Inhibitor,hematological,MRTX-9768,MTAP,CDKN2A
MRTX-9768 is a synthetic lethal-based inhibitor designed to bind the PRMT5-MTA complex and selectively target MTAP/CDKN2A-deleted tumors.
价 格：￥电议型 号：T9575产 地：中国大陆
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TN280220-O-Glucoginsenoside Rf20OGlucoginsenoside Rf,20 O Glucoginsenoside Rf
20-O-Glucoginsenoside Rf is a natural product extracted from Panax ginseng C. A. Mey.
价 格：￥电议型 号：TN2802产 地：中国大陆
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T9110Ceapin-A7UPR,Inhibitor,CeapinA7,stress,unfolded protein response,reticulum,Golgi,endoplasmic,Ceapin-
Ceapin-A7 is a selective blocker of ATF6α signaling in response to ER stress, with an IC50 of 0.59 μM. Ceapin-A7 can be used to explore both the mechanism of activation of ATF6α and its role in pathological settings.
价 格：￥电议型 号：T9110产 地：中国大陆
