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T6082SSR128129ESSR
SSR128129E is an allosteric and orally-active FGFR1 inhibitor (IC50: 1.9 μM), but not affecting other related RTKs.
价 格：￥电议型 号：T6082产 地：中国大陆
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T5048SSR240612
SSR240612 is a potent, and orally active specific non-peptide bradykinin B1 receptor antagonist (Kis = 0.48-0.73 and 358-481 nM for B1 and B2 receptors, respectively).
价 格：￥电议型 号：T5048产 地：中国大陆
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T11006Desmethyl ferroquineDesmethyl ferroquine,SSR97213,
Demethylferroquine is the activity and main metabolite of ironquine. Ironquin is an antimalarial drug. Demethylferroquinoline has obvious activity on chloroquine-sensitive and resistant Plasmodium falciparum strains.
价 格：￥电议型 号：T11006产 地：美洲
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T15276FerroquineFerroquine,Ferrochloroquine,SSR97193
Ferroquine is an antimalarial agent.
价 格：￥电议型 号：T15276产 地：美洲
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T5048SSR240612SSR240612
SSR240612 is a potent, and orally active specific non-peptide bradykinin B1 receptor antagonist (Kis = 0.48-0.73 and 358-481 nM for B1 and B2 receptors, respectively).
价 格：￥电议型 号：T5048产 地：美洲
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T6082SSR128129ESSR128129E,SSR,
SSR128129E is an allosteric and orally-active FGFR1 inhibitor (IC50: 1.9 μM), but not affecting other related RTKs.
价 格：￥电议型 号：T6082产 地：美洲
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T84293SSR 180；化合物 SSR 180SSR180711；SSR180711
SSR 180 is a potent and subtype-selective α7 agonist with applications in the study of Alzheimer;s disease and schizophrenia.
价 格：￥电议型 号：T84293产 地：中国大陆
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T69140Burapitant；化合物BurapitantSSR 240600；SSR 240600
Burapitant (SSR 240600) is a novel non-peptide tachykinin neurokinin 1 (NK) receptor antagonist with anti-coke oven and antidepressant activity.
价 格：￥电议型 号：T69140产 地：中国大陆
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T6082SSR128129E；化合物SSR128129ESSR；SSR
SSR128129E (SSR) is an allosteric and orally-active FGFR1 inhibitor (IC50: 1.9 μM), but not affecting other related RTKs.
价 格：￥电议型 号：T6082产 地：中国大陆
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T5048SSR240612；化合物SSR240612SSR240612
SSR240612 is a potent, and orally active specific non-peptide bradykinin B1 receptor antagonist (Kis = 0.48-0.73 and 358-481 nM for B1 and B2 receptors, respectively).
价 格：￥电议型 号：T5048产 地：中国大陆
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T40775SSR411298；SSR411298SSR411298；SSR411298
SSR411298 is a reversible, orally active compound that selectively inhibits fatty acid amide hydrolase (FAAH). Its potential lies in the field of post-traumatic stress disorder (PTSD) research.
价 格：￥电议型 号：T40775产 地：中国大陆
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T40398Crinecerfont hydrochloride；Crinecerfont hydrochlorideSSR-125543A|||SSR-125543 hydrochloride；SSR-1255
Crinecerfont hydrochloride (SSR-125543) is a highly potent, orally active, non-peptide antagonist of the CRF1 receptor. It has demonstrated efficacy in the context of Classic congenital adrenal hyperplasia (CAH) research.
价 格：￥电议型 号：T40398产 地：中国大陆
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T31095Crinecerfont；化合物CrinecerfontSSR125543|||SSR 125543|||SSR-125543|||SSR125543A|||SSR 125543A|||SSR-125
Crinecerfont (SSR-125543) is a selective antagonist of corticotropin-releasing factor 1 receptor (CRF1) and can be used in studies about Classic congenital adrenal hyperplasia.
价 格：￥电议型 号：T31095产 地：中国大陆
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T28858SSR504734；化合物 T28858SSR-504734|||SSR 504734；SSR-504734|||SSR 504734
SSR504734 is a novel potent glycine transporter 1 (GlyT1) inhibitor.
价 格：￥电议型 号：T28858产 地：中国大陆
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T28857SSR-182289A (Free)；化合物 T28857SSR182289|||SSR-182289A|||SSR-182289|||SSR 182289A|||SSR182289A|||SSR 1
SSR-182289A (Free) is a thrombin inhibitor.
价 格：￥电议型 号：T28857产 地：中国大陆
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T28856SSR180711 hydrochloride；SSR180711 盐酸盐SSR-180711A HCl|||SSR-180711C HCl|||SR-180711 HCl；SSR-180711A H
SSR180711 hydrochloride (SSR-180711A HCl) is a selective Alpha7 nicotinic acetylcholine partial agonist for the study of neurodegenerative and cognitive disorders.
价 格：￥电议型 号：T28856产 地：中国大陆
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T28855SSR126768A；化合物SSR126768ASSR-126768A|||SSR 126768A；SSR-126768A|||SSR 126768A
SSR126768A is a novel and selective, orally active and potent oxytocin (OT) receptor antagonist with inhibitory effects on uterine contractions for the prevention of preterm labor.
价 格：￥电议型 号：T28855产 地：中国大陆
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T28153Nelivaptan；化合物NelivaptanSSR149415|||SR 149415|||SR-149415；SSR149415|||SR 149415|||SR-149415
Nelivaptan (SR 149415) is a vasopressin V1b receptor antagonist.
价 格：￥电议型 号：T28153产 地：中国大陆
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T23395SSR 146977 hydrochloride；化合物 T23395SSR 146977 hydrochloride
NK3 receptor antagonist
价 格：￥电议型 号：T23395产 地：中国大陆
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T21989SSR 69071；化合物 T21989SSR 69071
SSR69071 is a potent, orally active, and selective inhibitor of neutrophil elastase. SSR69071 displays a higher affinity for human elastase (Ki =0.0168 nM) than for rat (Ki =3 nM), mouse (Ki =1.8 nM), and rabbit (Ki = 58 nM) elastases [2]. SSR69071 reduces myocardial infarct size following ischemia-reperfusion injury [1]. SSR69071 also has the potential for the treatment of chronic obstructive pulmonary diseases, asthma, emphysema, cystic fibrosis, and several inflammatory diseases.
价 格：￥电议型 号：T21989产 地：中国大陆
