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Thiazolidinone-Derivatives-1
Catalog No. A20355 Thiazolidinone-Derivatives-1 is an antiulcer agent which inhibits the secretion of gastric acid. 了解更多 -
Dolutegravir intermediate-1
Catalog No. A20351 integrase inhibitorDolutegravir is an integrase inhibitor developed for the treatment of human immunodeficiency virus (HIV)-l infection. 了解更多 -
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide
Catalog No. A20334 2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide is a compound that inhibits stress-induced ulcer and low toxicity, and can maintain the content of phospholipase A2 and prostaglandin E2 in ulcerated rats induced by water immersed restrained stress. 了解更多 -
Nucleocidin
Catalog No. A20329 Nucleocidin is an antitrypanosomal antibiotic, inhibiting the transfer of labeled amino acid from S-RNA to protein. 了解更多 -
Pemigatinib
Catalog No. A20312 FGFR inhibitorPemigatinib is a selective FGFR inhibitor in development for the treatment of patients with cholangiocarcinoma. 了解更多 -
CNS-5161 hydrochloride
Catalog No. A20308 NMDA ion-channel antagonistCNS-5161 hydrochloride is a novel NMDA ion-channel antagonist that interacts with the NMDA receptor/ion channel site to produce a noncompetitive blockade of the actions of glutamate. 了解更多 -
Tazanolast
Catalog No. A20296 Tazanolast is a selective mast-cell-stabilizing drug, on ozone-induced airway hyperresponsiveness in guinea pigs. 了解更多 -
Dexanabinol
Catalog No. A20290 Dexanabinol exhibits not only the antioxidant and neuroprotective activities in brain but also anti-inflammatory activity by inhibiting NF-κB and decreasing cytokines such as TNFα and interleukin-6, which could ensure the integrity of BBB and reduce cell apoptosis and death. 了解更多 -
Terbufibrol
Catalog No. A20276 Terbufibrol has been shown highly active in reducing serum total cholesterol (TC) levels in the normal and hypercholesterolemic male rat. 了解更多 -
N33-TEG-COOH
Catalog No. A20274 PROTAC linkerN33-TEG-COOH is a PROTAC linker containing four polyethylene glycol (PEG) units. 了解更多 -
1,2-Distearoyl-sn-glycero-3-phosphorylethanolamine
Catalog No. A20272 1,2-Distearoyl-sn-glycero-3-phosphorylethanolamine (DSPE) is a phosphoethanolamine (PE) lipid that can be used in the synthesis of liposomes. 了解更多 -
2-Aminoacridone
Catalog No. A20270 2-Aminoacridone is a widely used fluorophore (λexc=428 nm, λem=525 nm). 了解更多 -
Tefinostat
Catalog No. A20258 pan HDAC inhibitorTefinostat (CHR-2845) is a monocyte/macrophage-targeted pan HDAC inhibitor, cleaved into active acid CHR-2847 by the intracellular esterase human carboxylesterase-1 (hCE-1). Anti-monocytoid lineage leukaemias activity. 了解更多 -
α-2,3-sialyltransferase-IN-1
Catalog No. A20249 α-2,3-sialyltransferase inhibitorα-2,3-sialyltransferase-IN-1 (Lith-O-Asp analog) is a noncompetitive α-2,3-sialyltransferase inhibitor with an IC50 of 6 μM. 了解更多 -
Zabofloxacin
Catalog No. A20246 antibacterial candidate for clinical trialsZabofloxacin (DW-224a Free base) is a novel fluoronaphthyridone quinolone with a 7-pyrrolidone substituent that is considered a potent antibacterial candidate for clinical trials. 了解更多 -
PNU288034
Catalog No. A20241 -
Talazoparib tosylate
Catalog No. A20238 PARP1/2 inhibitorTalazoparib tosylate (BMN 673ts) is a novel, potent and orally available PARP1/2 inhibitor with an IC50 of 0.57 nM for PARP1. 了解更多 -
(S,R,S)-AHPC-PEG2-N3
Catalog No. A20234 E3 ligase ligand-linker conjugate(S,R,S)-AHPC-PEG2-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker used in PROTAC technology. 了解更多 -
Antibacterial compound 1
Catalog No. A20228 Antibacterial compound 1 is a oxazolidinone extracted from patent WO1999037630A1 with antibacterial activities. 了解更多 -
MAT2A inhibitor 1
Catalog No. A20226 MATA2 inhibitorsMAT2A inhibitor 1 is a methionine adenosyltransferase 2A (MATA2) inhibitor with an IC50 less than l00 nM. 了解更多 -
(S,R,S)-AHPC-PEG1-N3
Catalog No. A20223 E3 ligase ligand-linker conjugate(S,R,S)-AHPC-PEG1-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 1-unit PEG linker used in PROTAC technology. 了解更多 -
Rilmazafone
Catalog No. A20222 Rilmazafone is a water-soluble benzodiazepine prodrug that acts as a sedative and hypnotic neuropsychiatric agent. 了解更多 -
Foscarbidopa
Catalog No. A20221 dopamine receptor agonistFoscarbidopa (Carbidopa 4??-monophosphate) is a prodrug of Carbidopa, acts as a dopamine receptor agonist. 了解更多 -
(S,R,S)-AHPC-PEG4-N3
Catalog No. A20214 E3 ligase ligand-linker conjugate(S,R,S)-AHPC-PEG4-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 4-unit PEG linker used in PROTAC technology. 了解更多 -
Oxythiamine
Catalog No. A20210 vitamin B1 antagonistOxythiamine, an antimetabolite and a vitamin B1 antagonist, is a well-known thiamine antagonist and inhibitor of transketolase. 了解更多 -
JH-VIII-157-02
Catalog No. A20205 ALK inhibitorJH-VIII-157-02 is a structural analogue of alectinib, acts as an ALK inhibitor, and shows an IC50 of 2 nM for echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) G1202R in cells. 了解更多 -
(S,R,S)-AHPC-PEG3-NH2 hydrochloride
Catalog No. A20202 E3 ligase ligand-linker conjugate(S,R,S)-AHPC-PEG3-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 3-unit PEG linker used in PROTAC technology. 了解更多 -
Runcaciguat
Catalog No. A20200 soluble guanylate cyclase stimulatorRuncaciguat is an orally active stimulator of soluble guanylate cyclase, and is used in the research of cardiovascular and renal diseases combined with selective partial adenosine A1 receptor agonists. 了解更多 -
Levophacetoperane hydrochloride
Catalog No. A20198 Levophacetoperane inhibits in vitro in a competitive manner, norepinephrin uptake and dopamine uptake. 了解更多 -
(S,R,S)-AHPC-PEG2-NH2 hydrochloride
Catalog No. A20191 E3 ligase ligand-linker conjugate(S,R,S)-AHPC-PEG2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker used in PROTAC technology. 了解更多 -
Taminadenant
Catalog No. A20190 adenosine receptor antagonistTaminadenant is an antagonist of adenosine receptor. 了解更多 -
Irindalone
Catalog No. A20187 -
Thalidomide-O-amido-C4-NH2
Catalog No. A20184 E3 ligase ligand-linker conjugateThalidomide-O-amido-C4-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. 了解更多 -
(S,R,S)-AHPC-PEG4-NH2 hydrochloride
Catalog No. A20180 E3 ligase ligand-linker conjugate(S,R,S)-AHPC-PEG4-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 4-unit PEG linker used in PROTAC technology. 了解更多
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