Vitisin A

Base Information

Chemical Name:Vitisin A
CAS No.:142449-89-6
Molecular Formula:C56H42 O12
Molecular Weight:906.942
Hs Code.:
UNII:832N5294M6
ChEMBL ID:CHEMBL507409
DSSTox Substance ID:DTXSID901029696
Metabolomics Workbench ID:140487
Nikkaji Number:J975.028B
Wikidata:Q7937130
Wikipedia:Vitisin_A_(stilbenoid)
Mol file:142449-89-6.mol

Synonyms:vitisin A

Suppliers and Price of Vitisin A

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 11 raw suppliers

Chemical Property of Vitisin A

Chemical Property:

PSA：220.76000
LogP:10.72160
XLogP3:9.8
Hydrogen Bond Donor Count:10
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:7
Exact Mass:906.26762677
Heavy Atom Count:68
Complexity:1680

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C2C(C3=C4C(C(OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7=C(C=CC(=C7)C=CC8=C9C(C(OC9=CC(=C8)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O
Isomeric SMILES:C1=CC(=CC=C1[C@@H]2[C@H](C3=C4[C@@H]([C@H](OC4=CC(=C3)O)C5=CC=C(C=C5)O)C6=C2C(=CC(=C6)O)O)C7=C(C=CC(=C7)/C=C/C8=C9[C@@H]([C@H](OC9=CC(=C8)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O
Uses (+)-Vitisin A has been shown to reduce cell death and DNA fragmentation induced by sodium nitroprusside in SH-SY5Y cells and may contribute to protecting neuronal cells against nitrosative stress. Vitisin A is a natural phenol found in red wines. It is a pyranoanthocyanin.

Technology Process of Vitisin A

There total 1 articles about Vitisin A which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%