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T1582LNaproxen sodium萘普生钠；Miranax；Naprelan；Anaprox；RS-3650
Naproxen is a COX inhibitor for COX-1 and COX-2 with analgesic and antipyretic properties.
价 格：￥电议型 号：T1582L产 地：中国大陆
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T15656KGA-2727
KGA-2727 is a potent and selective SGLT1 inhibitor, with Kis of 97.4 nM and 43.5 nM for human and rat SGLT1, respectively. The selectivity ratios (Ki for SGLT2/Ki for SGLT1) of KGA-2727 are 140 (human) and 390 (rat). KGA-2727 for the treatment of diabete.
价 格：￥电议型 号：T15656产 地：中国大陆
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T15654Ketohexokinase inhibitor 1
Ketohexokinase inhibitor 1 is a ketohexokinase inhibitor (IC50s: 8.4 nM and 66 nM for KHK-C and KHK-A, respectively).
价 格：￥电议型 号：T15654产 地：中国大陆
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T1565DeferiproneCP20；Deferidone；去铁酮
Deferiprone is an Iron Chelator. The mechanism of action of deferiprone is as an Iron Chelating Activity.
价 格：￥电议型 号：T1565产 地：中国大陆
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T1553Chlorpheniramine maleateChlorphenamine maleate；NCI-C55265；马来酸氯苯那敏
Chlorphenamine is a histamine H1 antagonist used in allergic reactions, hay fever, rhinitis, urticaria, and asthma.
价 格：￥电议型 号：T1553产 地：中国大陆
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T15199EdicotinibJNJ-527；JNJ-40346527
Edicotinib is a brain penetrant and orally active inhibitor of the colony-stimulating factor-1 receptor (IC50: 3.2 nM). It shows less inhibitory effects on KIT and FLT3 (IC50: 20 nM and 190 nM). It has the potential for Alzheimer´s disease and rheumatoid
价 格：￥电议型 号：T15199产 地：中国大陆
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T14965Ciliobrevin D
Ciliobrevin D is a AAA+ ATPase motor cytoplasmic dynein inhibitor. Ciliobrevin D inhibits Hedgehog (Hh) signaling and primary cilia formation and it also inhibits dynein-dependent microtubule gliding and ATPase activity in vitro.
价 格：￥电议型 号：T14965产 地：中国大陆
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T1492Gemifloxacin mesylate甲磺酸吉米沙星；SB-265805S；LB-20304a；Gemifloxacin?mesylate
Gemifloxacin mesylate inhibits activities of DNA gyrase and topoisomerase IV, thereby inhibiting DNA replication and eventually bacterial growth. Gemifloxacin Mesylate is the mesylate salt form of gemifloxacin, a synthetic broad-spectrum fluoroquinolone w
价 格：￥电议型 号：T1492产 地：中国大陆
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T14871Carboxyamidotriazole OrotateL-651582 Orotate；CAI Orotate
Carboxyamidotriazole Orotate is a cytostatic inhibitor of nonvoltage-operated calcium channels and calcium channel-mediated signaling pathways. Carboxyamidotriazole Orotate (L-651582 Orotate) is the orotate salt form of Carboxyamidotriazole (CAI), an oral
价 格：￥电议型 号：T14871产 地：中国大陆
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T14865Carboprost tromethamine
Carboprost tromethamine is the synthetic 15-methyl analogue of prostaglandin F2α and it can effectively promote law contraction of the uterus and significantly reduce the amount of bleeding during and after delivery.
价 格：￥电议型 号：T14865产 地：中国大陆
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T1478Ondansetron hydrochloride dihydrate盐酸昂丹司琼；GR 38032；SN 307；Ondansetron hydrochloride；NSC 665799
Ondansetron hydrochloride is a competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties.
价 格：￥电议型 号：T1478产 地：中国大陆
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T14765BOS-172722
BOS-172722 is an inhibitor of monopolar spindle 1 (MPS1) checkpoint(IC50 of 2 nM).
价 格：￥电议型 号：T14765产 地：中国大陆
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T14687DeucravacitinibBMS-986165
BMS-986165 inhibits IL-12/23 and type I IFN pathways[1][2]. BMS-986165 is a highly selective, orally bioavailable allosteric TYK2 inhibitor for the treatment of autoimmune diseases. Which selectively binds to TYK2 pseudokinase (JH2) domain (IC50=1.0 nM) a
价 格：￥电议型 号：T14687产 地：中国大陆
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T14665LMotixafortide TFA(664334-36-5,Free)TF 14016 TFA；BKT140 TFA；T140 TFA；BL-8040 TFA
Motixafortide is an antagonist of CXCR4 with IC50 of ～1 nM. It induces the apoptosis of AML blasts by down-regulating ERK, BCL-2, MCL-1 and cyclin-D1 via altered miR-15a/16-1 expression.
价 格：￥电议型 号：T14665L产 地：中国大陆
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T1465Mupirocin莫匹罗星；Pseudomonic acid；BRL-4910A
Mupirocin is a RNA synthetase inhibitor antibacterial. It has shown excellent activity against gram-positive staphylococci and streptococci.
价 格：￥电议型 号：T1465产 地：中国大陆
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T14565BI-671800Cmpd A；AP-761
BI-671800 is a highly specific and potent antagonist of chemoattractant receptor-homologous molecule on Th2 cells (DP2/CRTH2). With IC50 values of 4.5 nM and 3.7 nM for PGD2 binding to CRTH2 in hCRTH2 and mCRTH2 transfected cells, respectively. BI-671800
价 格：￥电议型 号：T14565产 地：中国大陆
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T1439Lacidipine拉西地平；SN-305；GR-43659X；GX-1048
Lacidipine is a lipophilic dihydropyridine calcium antagonist with an intrinsically slow onset of activity. Due to its long duration of action, lacidipine does not lead to reflex tachycardia. It displays specificity in the vascular smooth muscle, where it
价 格：￥电议型 号：T1439产 地：中国大陆
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T14365AZ PFKFB3 26
AZ PFKFB3 26 is an effective and selective PFKFB3 inhibitor with an IC50 of 23 nM. The IC50s for PFKFB1 and PFKFB2 are 2.06 and 0.384 μM, respectively.
价 格：￥电议型 号：T14365产 地：中国大陆
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T1433Ritodrine hydrochlorideDU21220；NSC 291565；Ritodrine HCl；盐酸利托君
Ritodrine binds to and activates beta-2 adrenergic receptors of myometrial cells in the uterus, which decreases the intensity and frequency of uterine contractions. Ritodrine is a phenethylamine derivative with tocolytic activity. Specifically, ritodrine
价 格：￥电议型 号：T1433产 地：中国大陆
