Proanthocyanidin A1

Base Information

Chemical Name:Proanthocyanidin A1
CAS No.:103883-03-0
Molecular Formula:C30H24 O12
Molecular Weight:576.513
Hs Code.:
UNII:LX492GRN5W
Nikkaji Number:J454.256H
Wikipedia:Procyanidin_A1
Wikidata:Q105184985
Pharos Ligand ID:N2ZB14U2CHMR
Metabolomics Workbench ID:47865
ChEMBL ID:CHEMBL450916
Mol file:103883-03-0.mol

Synonyms:proanthocyanidin A-1;proanthocyanidin A1

Suppliers and Price of Proanthocyanidin A1

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

Usbiological
Procyanidin A1
5mg
$ 523.00

ChemScene
ProcyanidinA1 99.19%
10mg
$ 450.00

ChemScene
ProcyanidinA1 99.19%
5mg
$ 300.00

ChemScene
ProcyanidinA1 99.19%
1mg
$ 100.00

AvaChem
Procyanidin A1
20mg
$ 690.00

AvaChem
Procyanidin A1
10mg
$ 490.00

AvaChem
Procyanidin A1
1mg
$ 119.00

AvaChem
Procyanidin A1
5mg
$ 290.00

Arctom
ProcyanidinA1
10mg
$ 238.00

Total 41 raw suppliers

Chemical Property of Proanthocyanidin A1

Chemical Property:

Boiling Point:946.0±65.0 °C(Predicted)
PKA:8.77±0.70(Predicted)
PSA：209.76000
Density:1.766±0.06 g/cm3(Predicted)
LogP:2.79350
XLogP3:2.4
Hydrogen Bond Donor Count:9
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:2
Exact Mass:576.12677620
Heavy Atom Count:42
Complexity:986

Purity/Quality:

99%, ^*data from raw suppliers

Procyanidin A1 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O
Isomeric SMILES:C1[C@@H]([C@H](OC2=C1C(=CC3=C2[C@@H]4[C@H]([C@](O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O
Uses Procyanidin A1 is a type of procyanidin and is found in avocado, nuts and berries and may provide antioxidant activity as well as antiviral activity. Furthermore, some of its main metabolites have been shown to have prevention effects against (TNF)-?α-?stimulated adhesion of THP-?1 human monocytic cells.

Technology Process of Proanthocyanidin A1

There total 9 articles about Proanthocyanidin A1 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: 93.0%

: C₆₅H₁₉⁽²⁾H₃₅O₁₂

: 103883-03-0
procyanidin A1

Guidance literature:: With hydrogen; In tetrahydrofuran; methanol; water; at 20 ℃; for 3h; under 760.051 Torr;
DOI:10.1039/c9ob01896d

Reference yield: 73.0%

: C₈₆H₇₄O₁₃

: 103883-03-0
procyanidin A1

Guidance literature:: With 10 wt% Pd(OH)2 on carbon; hydrogen; In water; ethyl acetate; at 20 ℃; for 1.5h; Inert atmosphere;
DOI:10.1021/acs.orglett.5b00646