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Homogentisic acid
Catalog No. A12940 Homogentisic acid is a specific metabolite in urine and serum, which is used for diagnosis of alkaptonuria. 了解更多 -
CPA inhibitor
Catalog No. A11369 -
Pseudouridimycin
Catalog No. A18520 RNA polymerase 抑制剂Pseudouridimycin (PUM), an antibiotic, is a selective bacterial RNA polymerase (RNAP) inhibitor. Pseudouridimycin is a C-nucleoside analogue that is effective against both Gram-negative and Gram-positive bacteria. 了解更多 -
Taurodeoxycholate sodium salt
Catalog No. A18577 Taurodeoxycholate sodium salt is a bile salt-related anionic detergent used for isolation of membrane proteins including inner mitochondrial membrane proteins. Taurodeoxycholate (TDCA) inhibits various inflammatory responses. 了解更多 -
PF-06250112
Catalog No. A18612 BTK 抑制剂PF-06250112 is a potent, highly selective, orally bioavailable BTK inhibitor with an IC50 of 0.5 nM, shows inhibitory effect toward BMX nonreceptor tyrosine kinase and TEC with IC50s of 0.9 nM and 1.2 nM, respectively. 了解更多 -
5'-Deoxyadenosine
Catalog No. A18618 5'-deoxyadenosine, also known as 5'dAdo or 5'-dAdo, is a substrate of bacterial methylthioadenosine/S-adenosylhomocysteine (MTA/SAH) nucleosidase and a product inhibitor produced by radical SAM enzymes. 了解更多 -
Ureidopropionic acid
Catalog No. A18625 Ureidopropionic acid is an intermediate in the metabolism of uracil. 了解更多 -
AKOS B018304
Catalog No. A18719 AKOS B018304 is an arylalkylidene derivative, with polar substitution at para-position. 了解更多 -
BMS-986165
Catalog No. A18726 TYK2 抑制剂BMS-986165 is a Highly Potent and Selective Allosteric Inhibitor of TYK2. BMS-986165 Blocks Il-12, IL-23 and type I Interferon Signaling and Provides for Robust Efficacy in Preclinical Models of Inflammatory Bowel Disease. 了解更多 -
(-)-(S)-B-973B
Catalog No. A18761 α7 nAChR modulator-)-(S)-B-973B is a potent allosteric agonist and positive allosteric modulator of α7 nAChR, with antinociceptive activity. 了解更多 -
Bromperidol
Catalog No. A18254 Bromperidol, also known as Impromen and R-11333, is used as a means of long-term maintenance treatment of schizophrenia. Bromperidol is a close structural analogue of haloperidol. C3435T polymorphism is associated with some therapeutic response to bromperidol in schizophrenic patients, possibly by different drug concentration in the brain. 了解更多 -
Taltirelin
Catalog No. A18250 TRH-R agonistTaltirelin (TA0910) is a superagonist at thyrotropin-releasing hormone receptor (TRH-R) with an IC50 of 910 nM and EC50 of 36 nM for stimulating an increase in cytosolic Ca2+ concentration (Ca2+ release). 了解更多 -
Epristeride
Catalog No. A18231 5 alpha-reductase inhibitorEpristeride is a selective and specific uncompetitive inhibitor of human steroid 5 alpha-reductase isoform 2. 了解更多 -
Nifurtimox
Catalog No. A18227 Nifurtimox, an antiprotozoal agent, which is generally used for the treatment of infections with Trypanosoma cruzi, has been used in the therapy of neuroblastoma. Nifurtimox affects enzyme activity of lactate dehydrogenase (LDH). 了解更多 -
Bendazac L-lysine
Catalog No. A17975 Bendazac L-Lysine is one of agents that have been introduced for the management of cataracts, protecting the level of vision in patients, thus delaying the need for surgical intervention. 了解更多 -
Fondaparinux Sodium
Catalog No. A17918 factor Xa inhibitorFondaparinux sodium is a factor Xa inhibitor to form the high affinity binding site for the anti-coagulant factor antithrombin III (ATIII). 了解更多 -
Revaprazan Hydrochloride
Catalog No. A17506 Acid pump antagonistRevaprazan hydrochloride is a novel acid pump antagonist (APA). Revaprazan hydrochloride reduces COX-2 expression and has significant anti-inflammatory actions activities in H. pylori infection. 了解更多 -
Destruxin B
Catalog No. A18384 insecticidal and anticancerDestruxin B, isolated from entomopathogenic fungus Metarhizium anisopliae, is one of the cyclodepsipeptides with insecticidal and anticancer activities. Destruxin B induces apoptosis via a Bcl-2 Family-dependent mitochondrial pathway in human nonsmall cell lung cancer cells. 了解更多 -
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最新产品
AZ304
Catalog No. A17225 dual BRAF 抑制剂AZ304 is a potent dual BRAF inhibitor targeting the kinase domains of wild type BRAF, V600E mutant BRAF. AZ304 exerted potent inhibitory effects on both wild type and V600E mutant forms of the serine/threonine-protein kinase BRAF, with IC50 values of 79?nM and 38?nM, respectively. 了解更多 -
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最新产品
Fevipiprant
Catalog No. A17244 CRTh2 receptor antagonistFevipiprant, also known as NVP-QAW039 or QAW039, is an oral active and potent CRTh2 receptor antagonist and potentially useful for asthma treatment. 了解更多 -
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JNJ-38877618
Catalog No. A18325 c-Met inhibitorJNJ-38877618 is a novel potent, highly selective, orally bioavailable c-Met tyrosine kinase inhibitor with Kd of 1.2, 2.1 and 21 nM for WT, M1250T and Y1235D mutants MET, respectively. 了解更多 -
Porcn-IN-1
Catalog No. A18330 Potent porcupine inhibitorPorcn-IN-1 is potent porcupine inhibitor with an IC50 of 0.5??0.2 nM. 了解更多 -
Procyclidine HCl
Catalog No. A17371 Muscarinic antagonistProcyclidine hydrochloride is a muscarinic antagonist that crosses the blood-brain barrier and is used in the treatment of drug-induced extrapyramidal disorders and in Parkinsonism. 了解更多 -
Piromidic Acid
Catalog No. A17370 Piromidic acid is antibacterial against mainly gram negative organisms. It is used for urinary tract and intestinal infections. 了解更多 -
Tasimelteon
Catalog No. A17351 MT1 and MT2 receptor agonistTasimelteon is a melatonin MT1 and MT2 receptor agonist. 了解更多 -
Cinchonine (LA40221)
Catalog No. A17250 Cinchonine prevents High-Fat-Diet-Induced Obesity through downregulation of Adipogenesis and Adipose inflammation. 了解更多 -
GSK 2250665A
Catalog No. A17191 Itk 抑制剂GSK-2250665A是pKi = 9.2的Itk抑制剂，它对Aurora B激酶和Btk（pIC50值分别为6.4和6.5）和一组其他激酶表现出对Itk的选择性。 抑制PBMC中IFNγ的产生。 了解更多 -
Antineoplaston A10
Catalog No. A17183
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