Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN480373 (Rac)-Telmesteine 127657-29-8
(Rac)-Telmesteine is aproteaseinhibitor and is thus a suitable enzyme stabilizer extracted from patent WO 2017220302 A1, compound II-1. (Rac)-Telmesteine can be used as an enzyme stabilizer in protease-containing detergents and ...
YN260095 Tr-PEG6-OH 127999-16-0
Tr-PEG6-OH is a non-cleavable 6 unit PEGADClinker used in the synthesis of antibody-drug conjugates (ADCs).
YN320826 Veliflapon 128253-31-6
Veliflapon (BAY X 1005; DG-031) is an orally active and selective5-lipoxygenase activating protein (FLAP)inhibitor. Veliflapon inhibits the synthesis of theleukotrienes B4 and C4.
YN321205 KB-5492 anhydrous 129200-10-8
KB-5492 anhydrous is a potent and selective inhibitor ofsigma receptor, inhibits specific [3H]1,3-di(2-tolyl)guanidine (DTG) binding to thesigma receptor with an IC50 of 3.15μM. KB-5492 anhydrous is an anti-ulcer agent.
YN370013 ICI 211965 129424-08-4
ICI 211965 (ZM-211965) is a selective and orally potent5-Lipoxygenase(5-LPO) inhibitor.
MSA-2, a potent and orally available non-nucleotideSTINGagonist, hasEC50s of 8.3 and 24μM for human STING isoforms WT and HAQ, respectively. MSA-2 shows antitumor activity and stimulates interferon-β secret...
YN440196 Rp-8-CPT-cAMPS 129735-01-9
Rp-8-CPT-cAMPS, a cAMP analog, is a potent and competitive antagonist of cAMP-induced activation of cAMP-dependentPKA I and II. Rp-8-CPT-cAMPS preferentially selects site A of RI compares to site A of R...
YN250110 Rifalazil 129791-92-0
Rifalazil (KRM-1648; ABI-1648), a rifamycin derivative, inhibits the bacterial DNA-dependentRNA polymerase and kills bacterial cells by blocking off the β-subunit in RNA polymerase. Rifalazil (KRM-1648; ABI-1648) i...
YN370975 Sampatrilat 129981-36-8
Sampatrilat (UK-81252) is a potent and orally activevasopeptidaseinhibitor ofACE and neutral endopeptidase (NEP). Sampatrilat inhibits C-domain ACE (Ki=13.8nM) 12.4-fold more potent than that for the N-domain (Ki=171.9n...
YN321584 Levocetirizine 130018-77-8
Levocetirizine (LCZ, (R)-Cetirizine), the R-enantiomer of cetirizine, is an antagonist of histamine H(1) receptor.
YN322101 Levocetirizine dihydrochlorid... 130018-87-0
Levocetirizine is the active R-enantiomer of cetirizine and represents a new second-generation histamine H1 antagonist.
YN483983 C-Reactive Protein (CRP)... 130348-99-1
C-Reactive Protein (CRP) 201-206 is the 201-206 fragment of C-Reactive Protein. C-Reactive Protein (CRP), the prototypic marker of inflammation, is a cardiovascular risk marker and may promote atherogenesis.
YN483992 C-Reactive Protein (CRP)... 130349-01-8
C-Reactive Protein (CRP) 77-82 is the 77-82 fragment of C-Reactive Protein. C-Reactive Protein (CRP), the prototypic marker of inflammation, is a cardiovascular risk marker and may promote atherogenesis.
Bindarit exhibits selective inhibition against monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7 and MCP-2/CCL8.
YN250523 Quinaldopeptin 130743-07-6
Quinaldopeptin, a quinomycin antibiotic isolated from the culture ofStreptoverticillium albumstrain, is highly active against Gram-positive bacteria and anaerobes and strongly cytotoxic against cultured B16 melanoma cells.
YN330621 Benzoylgomisin O 130783-32-3
Benzoylgomisin O isolated fromSchis and ra rubriflora, has inhibitory activity against15-LOX,COX-1 and COX-2enzymes and anti-inflammatory activity.
YN310363 Decursinol angelate 130848-06-5
Decursinol angelate is a cytotoxic and protein kinase C activating agent from the root of Angelica gigas.
YN350230 Cornuside 131189-57-6
Cornuside is a secoiridoid glucoside isolated from the fruit ofCornus officinalisSieb. et Zucc., which is a traditional oriental medicine for treating inflammatory diseases and invigorating blood circulation. Cornuside inhibits mast ...
YN481206 (3R,5S)-Atorvastatin sodium 131275-93-9
(3R,5S)-Atorvastatin sodium is an impurity of Atorvastatin. Atorvastatin is an orally active HMG-CoA reductase inhibitor, has the ability to effectively decrease blood lipids. Atorvastatin inhibits human SV-SMC proliferation...
YN483750 PLP 139-151 131334-43-5
PLP (139-151) is amino acid residue 139 to 151 of myelin proteolipid protein (PLP) used to induce experimental autoimmune encephalomyelitis (EAE).
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