Irpexan

Irpexan

* Please be kindly noted products are not for therapeutic use. We do not sell to patients.

Category Others
Catalog number BBF-01505
CAS
Molecular Weight 606.87
Molecular Formula C36H62O7

Online Inquiry

Description

Irpexan is originally isolated from Irpex sp. 93028.

Specification

Synonyms 10-Hydroxy-11-(beta-D-mannopyranosyloxy)-2,6,10,15,19,23-hexamethyl-2,6,14,18,22-tetracosapentaene
IUPAC Name (2S,3S,4S,5S,6R)-2-[(6E,14E,18E)-10-hydroxy-2,6,10,15,19,23-hexamethyltetracosa-2,6,14,18,22-pentaen-11-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
Canonical SMILES CC(=CCCC(=CCCC(=CCCC(C(C)(CCC=C(C)CCC=C(C)C)O)OC1C(C(C(C(O1)CO)O)O)O)C)C)C
InChI InChI=1S/C36H62O7/c1-25(2)14-9-16-27(5)18-11-19-28(6)20-12-22-31(43-35-34(40)33(39)32(38)30(24-37)42-35)36(8,41)23-13-21-29(7)17-10-15-26(3)4/h14-15,18,20-21,30-35,37-41H,9-13,16-17,19,22-24H2,1-8H3/b27-18+,28-20+,29-21+/t30-,31?,32-,33+,34+,35+,36?/m1/s1
InChI Key AAEDIAWSKYSEKJ-ULWXIDRDSA-N

Properties

Appearance Colorless Oily Matter

Reference Reading

1. The irpexans, a new group of biologically active metabolites produced by the basidiomycete Irpex sp. 93028
S Silberborth, G Erkel, T Anke, O Sterner J Antibiot (Tokyo). 2000 Oct;53(10):1137-44. doi: 10.7164/antibiotics.53.1137.
Five novel antibiotics described as irpexans (1, 2, 3a, 3b, 4) were isolated from fermentations of an Irpex species in the course of a screening for new inhibitors of AP-1 and NF-kappaB mediated signal transduction pathways in COS-7 cells using secreted alkaline phosphatase (SEAP) as a reporter gene. The expression of an AP-1 and NF-kappaB driven SEAP reporter gene was inhibited in a dose dependent manner with 14-acetoxy-15-hydroxyirpexan (3b) being the most potent compound, followed by 14,15-irpexanoxide (2), 14,15-dihydroxyirpexan (3a) and 14-acetoxy-22,23-dihydro-15,23-dihydroxyirpexan (4). Irpexan (1) exhibited no activity. The irpexans (1, 2, 3a, 3b, 4) are characterized by weak cytotoxic but neither antibacterial nor antifungal activities. All five compounds are terpenoids with a mannose moiety. The structures were elucidated by spectroscopic methods.

Bio Calculators

Stock concentration: *
Desired final volume: *
Desired concentration: *

L

* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
g/mol
g

Recently viewed products

Online Inquiry

Verification code
cartIcon
Inquiry Basket