VD2173

  Cat. No.:  DC49803  
Chemical Structure
2574389-19-6
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More than 5000 active chemicals with high quality for research!
Field of application
VD2173 is a side chain cyclized macrocyclic peptide inhibitor of HGF-activating serine proteases. VD2173 potently inhibits matriptase and hepsin. VD2173 can be used for the research of lung cancer.
Cas No.: 2574389-19-6
Chemical Name: VD2173
Formula: C31H45N9O6S
M.Wt: 671.81
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC72681 SPC4061 SPC4061 an antisense nucleotide, is a potent PCSK9 inhibitor. SPC4061 targets the lock-in nucleic acid (LNA) of PCSK9 for the study of hypercholesterolemia and related diseases.
DC72680 PPACK II diTFA PPACK II diTFA is an irreversible and specific glandular and plasma kallikreins inhibitor.
DC72410 Ac-Phe-Gly-pNA Ac-Phe-Gly-pNA is the chymotrypsin specific substrate.
DC72409 AAF-CMK AAF-CMK is a TPPII (tripeptidylpeptidase II) inhibitor, shows anti-tumor activity and induces apoptosis. AAF-CMK can be used in leukemia research.
DC72231 Cyclotheonamide A Cyclotheonamide A is a serine protease inhibitor (cyclic polypeptide), which can be obtained from marine sponges of the genus Theonella. Cyclotheonamide A shows potent inhibitory activity against trypsin (Ki=0.023 µM) and streptokinase (Ki=0.035 µM) and moderate inhibitory activity against human α-thrombin (Ki=0.18 µM). Cyclotheonamide A can be used in study of antithrombotic.
DC72230 UAMC-00050 UAMC-00050 is a potent trypsin-like serine protease inhibitor. UAMC-00050 can be used in research of dry eye syndrome and ocular inflammation.
DC71824 Tilpisertib fosmecarbil Tilpisertib fosmecarbil is a potent serine/threonine kinase inhibitor. Tilpisertib fosmecarbil has anti-inflammatory activity.
DC71823 Bezeparsen Bezeparsen is a PCSK9 synthesis inhibitor.
DC71558 Chymotrypsin Chymotrypsin (Chymotrypsin A) is a serine protease produced by the pancreas. Chymotrypsin cleaves protein chains at the carboxyl side of aromatic amino acids.
DC71557 JO146 JO146 is a Chlamydia trachomatis high temperature requirement A (CtHtrA) protease inhibitor with IC50s of 21.86 and 1.15 μM for CtHtrA and human neutrophil elastase (HNE), respectively. JO146 can be used to inhibits bacterial infections.
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