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T13874RP 48497
RP 48497 is a photodegradation product of Eszopiclone. Eszopiclone is used in the treatment of insomnia.
价 格：￥电议型 号：T13874产 地：中国大陆
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T13397ZINC03129319
ZINC03129319 is an inhibitor of dengue virus (DENV) NS2B-NS3 protease.
价 格：￥电议型 号：T13397产 地：中国大陆
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T1326Gentamicin sulfate硫酸庆大霉素；Gentamycin sulfate；SCH9724；NSC-82261
Gentamycin Sulfate is a wide-spectrum, aminoglycoside antibiotic used to inhibit protein synthesis in sensitive organisms.
价 格：￥电议型 号：T1326产 地：中国大陆
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T12997SR-318
SR-318 potently inhibits the TNF-α release in whole blood (IC50 = 283 nM). SR-318 is a potent and highly selective inhibitor of p38 MAPK. The IC50 values are 5 nM, 32 nM and 6.11 μM for p38α, p38β and p38α/β, respectively.
价 格：￥电议型 号：T12997产 地：中国大陆
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T12979BI-3406
BI-3406 is an orally active, highly potent and selective between KRAS and Son of Sevenless 1 (SOS1) interaction inhibitor(IC50 : 6 nM),with anticancer activity.
价 格：￥电议型 号：T12979产 地：中国大陆
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T1297EugenolEugenic acid；Allylguaiacol；4-Allyl-2-methoxyphenol；4-Allylguaiacol；丁香酚
Eugenol is a Standardized Chemical Allergen. The physiologic effect of eugenol is by means of Increased Histamine Release and Cell-mediated Immunity.
价 格：￥电议型 号：T1297产 地：中国大陆
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T12930SKF89976A hydrochlorided,l-SKF89976A hydrochloride
SKF89976A hydrochloride is a selective inhibitor GABA transporter such as GAT-1 (IC50s = 0.28 μM), GAT-2 (IC50s = 137.34 μM) and GAT-3(IC50s = 202.8 μM) in CHO cells.
价 格：￥电议型 号：T12930产 地：中国大陆
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T12897LSHIN1RZ-2994
SHIN1 is an inhibitor of human serine hydroxymethyltransferse 1(SHMT1) with IC50 of 5 nM and human serine hydroxymethyltransferse 2 (SHMT2) with an IC50 of 13 nM.
价 格：￥电议型 号：T12897L产 地：中国大陆
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T12870SCH79797 dihydrochloride
SCH79797 dihydrochloride is an effective and selective antagonist of protease activated receptor 1 (PAR1) with an IC50 of 70 nM and a Ki of 35 nM. SCH79797 dihydrochloride has antiproliferative and pro-apoptotic effects.
价 格：￥电议型 号：T12870产 地：中国大陆
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T12854SBI-797812
SBI-797812 is structurally similar to active-site directed inhibitor of NAMPT(NAMPT with EC50 of 0.37 μM).
价 格：￥电议型 号：T12854产 地：中国大陆
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T1279VilazodoneSB659746A；EMD 68843；维拉佐酮
Vilazodone is a selective serotonin (5-HT) reuptake inhibitor (SSRI) and a 5-HT-1A receptor partial agonist, with antidepressant and anti-anxiety activities. Vilazodone inhibits the reuptake of serotonin from the synaptic cleft while stimulating the relea
价 格：￥电议型 号：T1279产 地：中国大陆
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T12695RBN-2397
RBN-2397 is a potent, selective and orally active accross species NAD+ competitive PARP7 inhibitor with IC50 less than 3 nM.
价 格：￥电议型 号：T12695产 地：中国大陆
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T12430PF-06821497
PF-06821497 is a selective and orally active Enhancer of Zeste Homolog 2 (EZH2) inhibitor, with robust tumor growth inhibition.
价 格：￥电议型 号：T12430产 地：中国大陆
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T12361ParcetasalMR-897
Parcetasal is a non-steroidal anti-inflammatory agent that can be used in pain relief studies.
价 格：￥电议型 号：T12361产 地：中国大陆
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T12297Oleuropeinic acid
Oleuropeinic acid is present initially in olive tissues or formed by the thermal treatment, possibly by the oxidation of oleuropein. Oleuropeinic acid is an antioxidant-soluble fiber.
价 格：￥电议型 号：T12297产 地：中国大陆
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T12097MorphothiadinGLS4；莫非赛定
Morphothiadin is a potent inhibitor on the replication of both wild-type and adefovir-resistant HBV (IC50 of 12 nM).
价 格：￥电议型 号：T12097产 地：中国大陆
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T11997MELK-IN-1尼达尼布杂质L；MELK inhibitor 17；Nintedanib Impurity L
MELK-IN-1 is a potent inhibitor of maternal embryonic leucine zipper kinase (MELK),(IC50:3nm;Ki:0.39 nM).
价 格：￥电议型 号：T11997产 地：中国大陆
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T1197Trimebutine maleatePolibutin；Debridat；马来酸曲美布汀
Trimebutine maleate is a weak mu-opioid agonist and has antimuscarinic effects. Trimebutine is an agonist of peripheral mu, delta, and kappa opiate receptors served as a spasmolytic drug for therapy of both chronic and acute abdominal pain.
价 格：￥电议型 号：T1197产 地：中国大陆
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T11897Telotristat ethylLX1606
Telotristat ethyl is a orally-delivered inhibitor of tryptophan hydroxylase that reduces serotonin production.
价 格：￥电议型 号：T11897产 地：中国大陆
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T11723LJNJ-39758979
JNJ-39758979 is a selective and high-affinity histamine H4 receptor antagonist (Kis: 12.5, 5.3, and 25 nM for human, mouse, and monkey histamine H4 receptor, respectively). JNJ-39758979 functionally antagonizes histamine-induced cAMP inhibition with a pA2
价 格：￥电议型 号：T11723L产 地：中国大陆
