Colletodiol

Base Information Edit

Chemical Name:Colletodiol
CAS No.:21142-67-6
Molecular Formula:C14H20O6
Molecular Weight:284.3
Hs Code.:
UNII:6044P09Y9J
Metabolomics Workbench ID:117680
Wikidata:Q27896955
Mol file:21142-67-6.mol

Synonyms:10-epi-colletodiol;colletodiol

Suppliers and Price of Colletodiol

Supply Marketing:Edit

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
Colletodiol
1mg
$ 165.00

Cayman Chemical
Colletodiol
1mg
$ 255.00

Total 3 raw suppliers

Chemical Property of Colletodiol Edit

Chemical Property:

PSA：93.06000
LogP:0.47780
XLogP3:0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:0
Exact Mass:284.12598835
Heavy Atom Count:20
Complexity:401

Purity/Quality:

99% ^*data from raw suppliers

Colletodiol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CC=CC(=O)OC(CC(C(C=CC(=O)O1)O)O)C
Isomeric SMILES:C[C@@H]1C/C=C/C(=O)O[C@@H](C[C@H]([C@@H](/C=C/C(=O)O1)O)O)C
Description Colletodiol is a fungal metabolite that has been found in D. grovesii and has immunosuppressant and antiviral activities. It inhibits concanavalin A- or LPS-induced proliferation of isolated mouse splenocytes (IC50s = 12 and 5 μg/ml, respectively). Colletodiol inhibits influenza A viral replication in HeLa-IAV-Luc cells.
Uses Colletodiol is a metabolite of Chaetomium funicola and an inhibitor of influenza A virus. Colletodiol can be used to synthesize Grahamimycin A and colletol.

Technology Process of Colletodiol

There total 49 articles about Colletodiol 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: 90.0%