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Chemical Structure Cat. No. Product Name CAS No.
N-(p-amylcinnamoyl) Anthranilic Acid Chemical Structure
BCP30845 N-(p-amylcinnamoyl) Anthranilic Acid 110683-10-8
N-(p-amylcinnamoyl) Anthranilic Acid (ACA) is a broad spectrum Phospholipase A2 (PLA2) inhibitor and TRP channel blocker. N-(p-amylcinnamoyl) Anthranilic Acid (ACA) is also an effective reversible inhibitor of calcium-activated chloride channels, has potential to treat arrhythmia.
Brevianamide F Chemical Structure
BCP24252 Brevianamide F 38136-70-8
Brevianamide F is a naturally occurring 2,5-diketopiperazine that possess interesting breast cancer resistance protein (BCRP) inhibitory activity.; also shows agonism towards Ca(2+)-channel activity at 100 uM, and has potentiation for use in the treatment of cardiovascular dysfunction.
YHO-13351 (free base) Chemical Structure
BCP28919 YHO-13351 (free base) 912288-64-3
YHO-13351 (free base) is the water-soluble prodrug of YHO-13177, which is a potent and specific inhibitor of BCRP.
YHO-13351 Chemical Structure
BCP28920 YHO-13351 1346753-00-1
YHO-13351 is the water-soluble prodrug of YHO-13177, which is a potent and specific inhibitor of BCRP.
Fumitremorgin C Chemical Structure
BCP28921 Fumitremorgin C 118974-02-0
Fumitremorgin C is a potent and selective ABCG2/BRCP inhibitor.
Lesinurad sodium Chemical Structure
BCP11514 Lesinurad sodium 1151516-14-1
Lesinurad sodium is a URAT1 and OAT inhibitor, is determined to be a substrate for the kidney transporters OAT1 and OAT3 with Km values of 0.85 and 2 µM, respectively.
Org 25935 hydrochloride Chemical Structure
BCP27717 Org 25935 hydrochloride 949588-40-3
Org-25935, also called SCH-900435, is a GlyT-1 inhibitor potentially for the treatment of schizophrenia and alcohol dependence.
ALX 5407 Chemical Structure
BCP21210 ALX 5407 571147-18-7
ALX 5407 is a potent, selective GlyT1 inhibitor that demonstrates >10-fold greater activity in in vitro functional glycine reuptake assay than racemic (±)-NFPS.
Vanoxerine Chemical Structure
BCP21322 Vanoxerine 67469-69-6
Vanoxerine (GBR12909) is a potent and selective DRI (Dopamine reuptake inhibitor).
Tetrabenazine Chemical Structure
BCP15831 Tetrabenazine 58-46-8
Tetrabenazine is a VMAT-inhibitor used for treatment of hyperkinetic movement disorder.
Mofezolac Chemical Structure
BCP30846 Mofezolac 78967-07-4
Mofezolac, also known as Disopain and N-22, is a cyclooxygenase-1 selective inhibitor used to treat pain, musculoskeletal pain, and arthritis.
Verdiperstat Chemical Structure
BCP30847 Verdiperstat 890655-80-8
Verdiperstat (AZD3241) is a selective, irreversible and orally active myeloperoxidase inhibitor, with an IC50 of 630 nM, and can be used in the research of neurodegenerative brain disorders.
JNJ-10229570 Chemical Structure
BCP30848 JNJ-10229570 524923-88-4
JNJ-10229570 is a novel MC1R and MC5R antagonist was used to treat primary human sebaceous cells. It might have a potential for the treatment of acne and other sebaceous gland pathologies.
Tyrosine kinase-IN-1 Chemical Structure
BCP30849 Tyrosine kinase-IN-1 705946-27-6
Tyrosine kinase-IN-1 is a multi-targeted tyrosine kinase inhibitor with IC50s of 4, 20, 4, 2 nM for KDR, Flt-1, FGFR1 and PDGFRα, respectively.
YF-2 Chemical Structure
BCP30850 YF-2 1311423-89-8
YF2 is a First-in-Class Histone Acetyltransferase (HAT) Activators for Precision Targeting of Epigenetic Derangements in Lymphoma.
Guanabenz Chemical Structure
BCP30851 Guanabenz 5051-62-7
Guanabenz is an alpha agonist of the alpha-2 adrenergic receptor that is used as an antihypertensive drug.
Radiprodil Chemical Structure
BCP30852 Radiprodil 496054-87-6
Radiprodil (RGH-896) is an orally active and selective NMDA NR2B antagonist. A potential therapeutic agent in treatment of neuropathic pain and possibly other chronic pain conditions.
CaCCinh-A01 Chemical Structure
BCP26187 CaCCinh-A01 407587-33-1
CaCCinh-A01 is an inhibitor of both TMEM16A and calcium-activated chloride channel (CaCC) with IC50s of 2.1 and 10 μM, respectively.
Shikonin Chemical Structure
BCP29329 Shikonin 517-89-5
Shikonin is a major component of a Chinese herbal medicine named zicao. Shikonin has shown various biological activities, including inhibition of TNF-α, NF-κB, HIV-1.
Sulfalen Chemical Structure
BCP30869 Sulfalen 152-47-6
Sulfalene is a long-acting plasma-bound sulfonamide used for respiratory and urinary tract infections and also for malaria.
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