Flavokawain A

Base Information

Chemical Name:Flavokawain A
CAS No.:37951-13-6
Molecular Formula:C₁₈H₁₈O₅
Molecular Weight:314.338
Hs Code.:
European Community (EC) Number:636-475-1
NSC Number:37445
UNII:8OM2XZ2ZM3
DSSTox Substance ID:DTXSID601317535
Nikkaji Number:J754.134A,J107.409A
Wikipedia:Flavokavain_A
Wikidata:Q5458164
Metabolomics Workbench ID:46119
ChEMBL ID:CHEMBL243829
Mol file:37951-13-6.mol

Synonyms:flavokavin A;flavokawain A

Suppliers and Price of Flavokawain 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

TRC
FlavokawainA
250mg
$ 385.00

ChemScene
(E)-FlavokawainA 99.29%
10mg
$ 90.00

ChemScene
(E)-FlavokawainA 99.29%
5mg
$ 50.00

ChemScene
(E)-FlavokawainA 99.29%
20mg
$ 150.00

AvaChem
Flavokavain A
5mg
$ 95.00

AvaChem
Flavokavain A
25mg
$ 369.00

AvaChem
Flavokavain A
10mg
$ 189.00

Arctom
(E)-1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one 97%
250mg
$ 769.00

Arctom
(E)-1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one 97%
100mg
$ 513.00

American Custom Chemicals Corporation
FLAVOKAWAIN A 95.00%
5MG
$ 495.10

Total 18 raw suppliers

Chemical Property of Flavokawain A

Chemical Property:

Melting Point:113-114℃
Boiling Point:529.9±50.0 °C(Predicted)
PKA:6.88±0.40(Predicted)
Density:1?+-.0.06 g/cm3(Predicted)
XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:314.11542367
Heavy Atom Count:23
Complexity:400

Purity/Quality:

≥98% ^*data from raw suppliers

FlavokawainA ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2OC)OC)O
Isomeric SMILES:COC1=CC=C(C=C1)/C=C/C(=O)C2=C(C=C(C=C2OC)OC)O
Uses Flavokawain A is a?chalcone found in the kava plant. It induces apoptosis in bladder cancer cells via a Bax protein-dependent and mitochondria-dependent apoptotic pathway. Furthermore, natural chalcones have been?implicated as lead compounds for developing dual inhibitors against?histone deacetylase enzymes (HDACs)?and NF-κB.

Technology Process of Flavokawain A

There total 15 articles about Flavokawain 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: 99.0%