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Chemical Structure Cat. No. Product Name CAS No.
Lanifibranor Chemical Structure
BCP29124 Lanifibranor 927961-18-0
Lanifibranor is a peroxisome proliferator-activated receptors (PPAR) agonist.
Artemisitene Chemical Structure
BCP39891 Artemisitene 101020-89-7
Artemisitene is a derivative of Artemether.
4-(6-Methacryloyloxyhexyloxy)phenol Chemical Structure
BCP49675 4-(6-Methacryloyloxyhexyloxy)phenol 142627-92-7
2-Ethylisothiazolidine 1,1-dioxide Chemical Structure
BCP49674 2-Ethylisothiazolidine 1,1-dioxide 73343-04-1
RAS-IN-2 Chemical Structure
BCP49648 RAS-IN-2 2765081-21-6
RAS-IN-2 (RMC-6236) is a potent pan-KRAS inhibitor targeting activation-state KRAS for cancer-related studies.
Adipostatin A Chemical Structure
BCP33965 Adipostatin A 3158-56-3
Adipostatin A is found in barley. Adipostatin A is isolated from cereals and other plant.
Forskolin Chemical Structure
BCP07063 Forskolin 66575-29-9
Forskolin is a labdane diterpenoid with antihypertensive, positive inotropic, platelet aggregation inhibitory and adenylate cyclase activating properties. The activation of adenylate cyclase results in increased intracellular cyclic AMP in most tissue and cells.
Methoxatin disodium salt Chemical Structure
BCP16823 Methoxatin disodium salt 122628-50-6
Methoxatin disodium salt is used as a cofactor (prosthetic group) for enzyme-catalyzed redox reactions of glucose and methanol dehydrogenase(s).
Ivacaftor Chemical Structure
BCP01857 Ivacaftor 873054-44-5
Ivacaftor is a CFTR activator (IC50 of 43 ± 38 nM).
MTX115325 Chemical Structure
BCP49673 MTX115325 2750895-97-5
MTX115325 is an orally active, brain-penetrating USP30 inhibitor (IC50=12 nM) with neuroprotective activity.
ARV393 Chemical Structure
BCP49670 ARV393 2851885-95-3
ARV-393 is an orally active PROTAC degrader targeting BCL6. ARV-393 utilizes the ubiquitin-proteasome system to target the degradation of BCL6. ARV-393 has DC50 and GI50 values of <1 nM in multiple cell lines of diffuse large B-cell lymphoma (DLBCL) and Burkitt lymphoma (BL). ARV-393 also demonstrated considerable tumor suppressor activity in tumor xenograft models.
Hematin porcine Chemical Structure
BCP49671 Hematin porcine 15489-90-4
Hematin is an iron-containing porphyrin. It is used for testing in vitro activities of the Rx-01 oxazolidinones against hospital and community pathogens.
Decapeptide-4 Chemical Structure
BCP49672 Decapeptide-4 Decapeptide-4
Decapeptide-4 is a synthetic peptide consisting of arginine, aspartic acid, cysteine, glutamic acid, leucine, methionine and tyrosine.
Yakuchinone B Chemical Structure
BCP41124 Yakuchinone B 81840-57-5
EGT1442 Chemical Structure
BCP03928 EGT1442 1118567-05-7
Bexagliflozin(EGT1442) is a potent and selective SGLT2 inhibitor with IC50 value of 5.6 μM /2 nM in SGLT1 /SGLT2 respectively.
rac-Clopidogrel Hydrogen Sulfate Chemical Structure
BCP04255 rac-Clopidogrel Hydrogen Sulfate 135046-48-9
rac-Clopidogrel Hydrogen Sulfate is used in the synthesis of Clopidogrel derivatives as platelet aggregation inhibitors.
Erdafitinib Chemical Structure
BCP20346 Erdafitinib 1346242-81-6
Erdafitinib (JNJ-42756493) is a potent and orally available FGFR family inhibitor; inhibits FGFR1-4 with IC50 values of 1.2, 2.5, 3.0 and 5.7nM, respectively.
Terbutaline sulfate Chemical Structure
BCP09034 Terbutaline sulfate 23031-32-5
Terbutaline sulfate is a β2-adrenergic receptor agonist; a fast-acting bronchodilator and a tocolytic to delay premature labor.
Silymarin Chemical Structure
BCP13563 Silymarin 65666-07-1
Silymarin, a strong novel free radical scavenger, is used for treatment of patients with acute brain infarction.
RMC-7977 Chemical Structure
BCP49669 RMC-7977 2765082-12-8
RMC-7977 is a reversible, tri-complex RAS inhibitor with broad spectrum activity for both mutant and wild-type (WT) KRAS, NRAS, and HRAS variants.
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