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TN12613-O-Caffeoylquinic acid methyl esterInhibitor,inhibit,3 O Caffeoylquinic acid methyl ester,3OCaffeoy
3-O-Caffeoylquinic acid methyl ester is a natural product from Morus alba L.
价 格：￥电议型 号：TN1261产 地：中国大陆
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T60123Chimmitecan
Chimmitecan is a potent inhibitor of topoisomerase I and displays outstanding activity in vitro and in vivo.
价 格：￥电议型 号：T60123产 地：中国大陆
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T7622GabazineInhibitor,Gamma-aminobutyric acid Receptor,Gabazine,γ-Aminobutyric acid Receptor,inhibit,SR
Gabazine is an antagonist of GABAA receptors (Ki : 74-150 nM)
价 格：￥电议型 号：T7622产 地：中国大陆
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TP2212La-MSH, amide Acetate(581-05-5 free base)a MSH, amide Acetate(581 05 5 free base),aMSH, amide Acetate
a-MSH, amide Acetate as an endogenous neuropeptide. It is an endogenous melanocortin receptor 4 (MC4R) agonist with anti-inflammatory and antipyretic activities. α-MSH is a post-translational derivative of pro-opiomelanocortin (POMC)
价 格：￥电议型 号：TP2212L产 地：中国大陆
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T67742EX-A5386
EX-A5386 is a potent glucocorticoid receptor modulator, IC50/EC50<100nM.
价 格：￥电议型 号：T67742产 地：中国大陆
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TQ0029ASTX660Inhibitor,inhibit,ASTX-660,ASTX660,IAP,ASTX 660
ASTX660 is an orally bioavailable dual antagonist of cIAP and XIAP.
价 格：￥电议型 号：TQ0029产 地：中国大陆
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TN71672,4,5-Tribromoimidazole
2,4,5-Tribromoimidazole is a marine derived natural products found in Hexaplex trunculus.
价 格：￥电议型 号：TN7167产 地：中国大陆
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T37082HS271HS271,HS-271
HS271 is a selective, highly potent and orally active IRAK4 inhibitor (IC50= 7.2 μM). HS271 shows excellent enzymatic and cellular activities, as well as excellent pharmacokinetic properties.
价 格：￥电议型 号：T37082产 地：中国大陆
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TQ0271Falnidamol
Falnidamol is an orally active, selective EGFR tyrosine kinase inhibitor with an IC50 of 3 nM. Falnidamol displays > 1000-fold lower potency against ErbB2 (IC50=3.4 μM) and a range of other related tyrosine kinases (IC50>10 μM). Falnidamol is a pyrimido-pyrimidine compound and has anti-cancer activity.
价 格：￥电议型 号：TQ0271产 地：中国大陆
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T7295MiridesapGSK 2315698,GSK-2315698,Miridesap,Inhibitor,inhibit
Miridesap is a divalent crosslinker of SAP that causes rapid depletion of circulating SAP via hepatic clearance. It also produces significant reduction of SAP from cerebrospinal fluid and visceral amyloid deposits
价 格：￥电议型 号：T7295产 地：中国大陆
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T7604ValrubicinInhibitor,AD 32,AD32,Valrubicin,inhibit,PKC,Antibiotic,Protein kinase C
Valrubicin (AD 32) inhibits TPA- and PDBu-induced PKC activation (IC50s: 0.85 and 1.25 μM) and has antitumor and anti-inflammatory activity.
价 格：￥电议型 号：T7604产 地：中国大陆
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TCS0102PulegoneEndogenous Metabolite,Transient receptor potential channels,TRP Channel,Pulegone,Inhibitor,i
1. Pulegone has cytotoxicity followed by regenerative cell proliferation is the MOA for Pulegone-induced urothelial tumors in female rats. 2. Pulegone induces a verapamil-sensitive psychostimulant effect that appears to independ on the opening of L-type calcium channels. 3. Pulegone has negative reinforcing properties and seems to possess anxiolytic-like actions unrelated to the benzodiazepine site of the γ-aminobutyric acid type A (GABAA) receptor.
价 格：￥电议型 号：TCS0102产 地：中国大陆
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T8234ML401ML401,Inhibitor,ML 401,EBI2/GPR183,inhibit,ML-401
ML401 is a selectively EBI2(GPR183) receptor antagonist(IC50 of 1.03 nM) .
价 格：￥电议型 号：T8234产 地：中国大陆
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TN6732Oenothein Bantitumor,HCV,Hepatitis C virus,ellagitannin,antifungal,antioxidant,Bacterial,inhibit,Oen
Oenothein B is a specific inhibitor of poly(ADP-ribose) glycohydrolase. Oenothein B shows antioxidant, anti-inflammatory, antifungal, anti-HCV, and antitumor properties.
价 格：￥电议型 号：TN6732产 地：中国大陆
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T79823,6-Dihydroxyflavoneinhibit,Inhibitor,caspase cascade,cell viability,oxidative stress,3,6-DHF,Apopto
3,6-Dihydroxyflavone suppresses the epithelial-mesenchymal transition in breast cancer cells by inhibiting the Notch signaling pathway.
价 格：￥电议型 号：T7982产 地：中国大陆
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T63812MrgprX2 antagonist-8
MrgprX2 antagonist-8 is an MrgprX2 antagonist that can be used to study inflammatory diseases.
价 格：￥电议型 号：T63812产 地：中国大陆
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T9753LEI110HepG2 cells,inhibit,thiol hydrolases,LEI110,Inhibitor,LEI-110,lipolysis,Phospholipase,LEI 110
LEI110 is a potent Phospholipase A2, group XVI (PLA2G16) inhibitor with an Ki value of 20 nM. LEI110 is a selective pan-inhibitor of the HRASLS family of thiol hydrolases (i.e., PLA2G16, HRASLS2, RARRES3 and iNAT).
价 格：￥电议型 号：T9753产 地：中国大陆
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T9519EliapixantInhibitor,chronic,Eliapixant,cough,refractory,BAY-1817080,P2X Receptor,BAY1817080,P2X3,inh
Eliapixant (BAY 1817080) is a potent and selective P2X3 receptor antagonist, with an IC50 of 8 nM. Eliapixant can be used for the research of refractory chronic cough.
价 格：￥电议型 号：T9519产 地：中国大陆
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T9834(3Z)-1-methyl-3-[2-(4-methylphenyl)-2-oxo-ethylidene]piperazin-2-one(3Z) 1 methyl 3 [2 (4 methylphen
(3Z)-1-methyl-3-[2-(4-methylphenyl)-2-oxo-ethylidene]piperazin-2-one is a chemical agent.
价 格：￥电议型 号：T9834产 地：中国大陆
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T23003ML337
ML337 is a negative allosteric modulator of mGlu3 with an IC50 of 593 nM.
价 格：￥电议型 号：T23003产 地：中国大陆
