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￥ 0.00 “AG 013736”的搜索结果
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Sigma-2 receptor antagonist 1
Catalog No. A20310 sigma-2 (??-2) receptor antagonistSigma-2 receptor antagonist 1 is a sigma-2 (??-2) receptor antagonist. 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 -
Fosmidomycin sodium salt
Catalog No. A20292 Fosmidomycin sodium salt is a phosphonic acid antibiotic and a antimalarial drug, which is active against both Gram-negative and Gram-positive bacteria. 了解更多 -
Telratolimod
Catalog No. A20289 TLR7/8 agonistTelratolimod is a toll like receptors 7/8 (TLR7/8) agonist, with antitumor activity. 了解更多 -
Abaperidone
Catalog No. A20286 5-HT2A/dopamine D2 antagonistAbaperidone is a potent antagonist of 5-HT2A?receptor and dopamine D2 receptor with IC50s of 6.2 and 17 nM. 了解更多 -
Lidanserin
Catalog No. A20266 5-HT2A/α1-adrenergic receptor antagonistLidanserin is a drug which acts as a combined 5-HT2A and α1-adrenergic receptor antagonist. 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 -
Spirendolol
Catalog No. A20254 β adrenergic receptor antagonistSpirendolol is a β adrenergic receptor antagonist. 了解更多 -
Masupirdine free base
Catalog No. A20245 5-HT6 receptor antagonistMasupirdine free base (SUVN-502 free base) is a potent, selective, orally bioavailable, and brain penetrant 5-HT6 receptor antagonist (Ki of 2.04 nM for human 5-HT6 receptor). 了解更多 -
RORγt Inverse agonist 2
Catalog No. A20243 RORγt inverse agonistRORγt Inverse agonist 2 is a selective, orally active RORγt inverse agonist with an EC50 of 119 nM. 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 -
SSTR5 antagonist 1
Catalog No. A20218 SSTR5 antagonistSSTR5 antagonist 1 is a potent, selective, and orally available somatostatin receptor subtype 5 (SSTR5) antagonist with IC50s of 9.6 and 57 nM for hSSTR5 and mSSTR5, respectively. (Compound 25a). 了解更多 -
Foslevodopa
Catalog No. A20212 -
ALB-127158(a)
Catalog No. A20211 MCH1 receptor antagonistALB-127158(a) is a potent and selective melanin concentrating hormone 1 (MCH1) receptor antagonist. 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 -
NK-1 Antagonist 1
Catalog No. A20201 NK-1 receptor antagonistNK-1 Antagonist 1 (Rolapitant intermediate) is an antagonist of NK-1 receptor, used in the research of NK-1 related diseases and conditions such as cough, overactive bladder, alcohol dependency and depression. 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 -
GPR84 antagonist 8
Catalog No. A20193 -
Taminadenant
Catalog No. A20190 adenosine receptor antagonistTaminadenant is an antagonist of adenosine receptor. 了解更多 -
Oral antiplatelet agent 1
Catalog No. A20188 Oral antiplatelet agent 1 is a potent antiplatelet agent with an IC50 of 2.94 μM in vitro as well as antithrombotic efficacy in a rat model. P2Y receptor antagonist. 了解更多 -
Irindalone
Catalog No. A20187 -
(S,R,S)-AHPC-PEG6-C4-Cl
Catalog No. A20169 (S,R,S)-AHPC-PEG6-C4-Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 6-unit PEG linker. (S,R,S)-AHPC-PEG6-C4-Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays. 了解更多 -
FK1052 hydrochloride
Catalog No. A20164 5-HT3 /5-HT4 receptor dual antagonistFK1052 hydrochloride is a potent 5-HT3 and 5-HT4 receptor dual antagonist. 了解更多 -
(S,R,S)-AHPC-(C3-PEG)2-C6-Cl
Catalog No. A20157 (S,R,S)-AHPC-(C3-?PEG)?2-?C6-?Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker. (S,R,S)-AHPC-(C3-?PEG)?2-?C6-?Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays. 了解更多 -
5-HT7 agonist 1
Catalog No. A20143 5-HT7 receptor agonist5-HT7 agonist 1 is a selective 5-HT7 receptor agonist, with an IC50 of 222.93 nM, can be used for the 5-HT7 receptor related disease, such as CNS disorders. 了解更多 -
Ceftobiprole
Catalog No. A20135 Ceftobiprole is a broad-spectrum cephalosporin with activity against Methicillin-resistant staphylococcus aureus (MRSA) with the MIC90 value of 2 mcg/mL. 了解更多 -
GRK2-IN-1
Catalog No. A20131 GRKs-IN-1, Compound 14as, has remarkable potency against and selectivity for G protein-coupled receptor kinase 2 GRK2 (IC50=30 nM) and GRK5 (IC50=7.1 μM). GRKs-IN-1 is a derivative 14as of paroxetine, shows a 100-fold improvement in cardiomyocyte contractility assays over paroxetine. 了解更多 -
GPR40/FFAR1 modulator 1
Catalog No. A20129 GPR40/FFAR1 agonistGPR40/FFAR1 modulator 1 is an agonist and an allosteric modulator for Gq-coupled free fatty acid receptor 1 (GPR40/FFAR1). 了解更多 -
Losmiprofen
Catalog No. A20115 -
Saredutant
Catalog No. A20096 -
Pparδ agonist
Catalog No. A20088 PPARδ agonistPPARδ agonist is a PPARδ agonist extracted from patent US20180071304, compound example 10. 了解更多 -
Gemcabene
Catalog No. A20083
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