Chemical
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- Catálogos PDF
Chemical Hay 28543 productos.
β-Melanocyte Stimulating Hormone TFA, human
β-Melanocyte Stimulating Hormone TFA, human is a 22-residue peptide, which acts as an endogenous melanocortin-4 receptor (MC4-R) agonist.
Luteolin-7-O-β-D-glucopyranoside
Luteolin-7-O-β-D-glucopyranoside is one of the chemical constituents of the aerial parts of codonopsis nervosa.
Tricin
Tricin is a natural flavonoid that is abundant in rice bran. Tricin inhibits HCMV replication by inhibiting CDK9. Tricin inhibits proliferation and invasion of C6 glioma cells by upregulating faK-targeted microrNA-7 expression.
Angiopeptin TFA
Angiopeptin TFA, a cyclic octapeptide analog of somatostatin, is an SST2 / SST5 receptor partial agonist with IC50 values of 0.26 nM and 6.92 nM, respectively. Angiopeptin TFA inhibits growth hormone release and insulin-like growth factor-1 (IGF-1) production. Angiopeptin TFA inhibits adenylate cyclase or stimulates extracellular acidification....
Deltorphin 2 TFA
Deltorphin 2 TFA is a selective peptide agonist for the δ opioid receptor.
Oteseconazole
Oteseconazole (VT-1161) is an antifungal compound with oral activity that is highly selective for CYP51. It can effectively bind to and inhibit CYP51 of N. albicans (Kd
Dehydroandrographolide succinate
Dehydroandrographolide succinate, extracted from herbal medicine Andrographis paniculata (Burm f) Nees, has immunostimulatory, anti-infective and anti-inflammatory effect.
Escitalopram Oxalate
Escitalopram Oxalate is a selective serotonin (5-HT) reuptake inhibitor (SSRI) with Ki of 0.89 nM.
BMS-986020
BMS-986020 (also known as AM152) is a potent and selective LPA1 antagonist.
GSK690693
GSK690693 is a potent Akt inhibitor (Akt1 IC50 = 2 nM, Akt2 IC50 = 13 nM, Akt3 IC50 = 9 nM) which also inhibited the phosphorylation of the downstream target GSK3b in cells.
Rizatriptan Benzoate
Rizatriptan Benzoate is an agonist at serotonin 5-HT1B and 5-HT1D receptors. Rizatriptan blocks neurogenic vasodilation via an action on 5-HT(1D) receptors located on perivascular trigeminal nerves to inhibit CGRP release in anaesthetized guinea-pigs.
EMI1
EMI1 is an EGFR ex19del/T790M/C797S and EGFR L858R/T790M/C797S inhibitor. EMI1 can be used for the research of mutant EGFR-associated, drug-resistant non-small-cell lung cancer (NSCLC).