Sclerotiorin (Q15424763)

Sclerotiorin (English)

21 September 2016

chemical formula

C₂₁H₂₃ClO₅

1 reference

Sclerotiorin (English)

21 September 2016

canonical SMILES

CCC(C)C=C(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CO1)(C)OC(=O)C)Cl

1 reference

Sclerotiorin (English)

21 September 2016

isomeric SMILES

CC[C@H](C)/C=C(\C)/C=C/C1=CC2=C(C(=O)[C@](C(=O)C2=CO1)(C)OC(=O)C)Cl

1 reference

Sclerotiorin (English)

21 September 2016

found in taxon

Penicillium sclerotiorum

4 references

Chlamydospore-like cell-inducing substances of fungi: Close correlation between chemical reactivity with methylamine and biological activity.

Azaphilones with endothelin receptor binding activity produced by Penicillium sclerotiorum: taxonomy, fermentation, isolation, structure elucidation and biological activity.

Azaphilone and isocoumarin derivatives from the endophytic fungus Penicillium sclerotiorum PSU-A13.

Sclerotiorine, C(20)H(20)O(5)Cl, a chlorine-containing metabolic product of Penicillium sclerotiorum van Beyma

Penicillium multicolor

2 references

Isochromophilones I and II, novel inhibitors against gp120-CD4 binding produced by Penicillium multicolor FO-2338. I. Screening, taxonomy, fermentation, isolation and biological activity.

Studies in the biochemistry of micro-organisms. Metabolic products of Penicillium multicolor G.-M. and P. with special reference to sclerotiorin

Pyrenula japonica

1 reference

Production of Xanthones with Free Radical Scavenging Properties, Emodin and Sclerotiorin by the Cultured Lichen Mycobionts of Pyrenula japonica

Penicillium citreonigrum

1 reference

Chemical epigenetics alters the secondary metabolite composition of guttate excreted by an atlantic-forest-soil-derived Penicillium citreonigrum

Arcopilus aureus

1 reference

Bioactive metabolites from Chaetomium aureum: structure elucidation and inhibition of the Hsp90 machine chaperoning activity.

described by source

Synthesis of the azaphilones (+)-sclerotiorin and (+)-8-O-methylsclerotiorinamine utilizing (+)-sparteine surrogates in copper-mediated oxidative dearomatization

0 references

Identifiers

InChI

InChI=1S/C21H23ClO5/c1-6-12(2)9-13(3)7-8-15-10-16-17(11-26-15)19(24)21(5,27-14(4)23)20(25)18(16)22/h7-12H,6H2,1-5H3/b8-7+,13-9+/t12-,21+/m0/s1

1 reference

Sclerotiorin (English)

SWJLTKXURNHVHE-UPWXJBBJSA-N

21 September 2016

InChIKey

1 reference

SWJLTKXURNHVHE-UPWXJBBJSA-N

Sclerotiorin (English)

21 September 2016

1 reference

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=549-23-5

1 reference

(+)-Sclerotiorin (English)

21 September 2016

1 reference

Sclerotiorin (English)

21 September 2016

ChEBI ID

186034

mapping relation type

exact match

1 reference

ChEBI release 2022-06-13

1 reference