(Q27106920)

(1R,2R,5R)-1,5-dihydroxy-2-(hydroxymethyl)-2,5,7-trimethylspiro[1H-indene-6,1'-cyclopropane]-4-one

Illudin S (English)

5 October 2016

1 reference

1 reference

C₁₅H₂₀O₄

1 reference

Illudin S (English)

19 November 2016

CC1=C2C(C(C=C2C(=O)C(C13CC3)(C)O)(C)CO)O

1 reference

Illudin S (English)

19 November 2016

CC1=C2[C@H]([C@](C=C2C(=O)[C@](C13CC3)(C)O)(C)CO)O

1 reference

Illudin S, the sole antiviral compound in mature fruiting bodies of Omphalotus illudens

Illudin S (English)

19 November 2016

5 references

CELL-FREE BIOSYNTHESIS OF PEPTIDE ANTIBIOTICS

Isolation of Illudin S from the Mature Basidiocarp ofOmphalotus Illudens, and Isolation of Illudins S and M from the Fermentation Broth ofOmphalotus Olearis

Structure-activity relationships of illudins: analogs with improved therapeutic index

Sesquiterpenes from Omphalotus illudens

Omphalotus guepiniiformis

1 reference

Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro

Omphalotus olearius

3 references

Isolation of Illudin S from the Mature Basidiocarp ofOmphalotus Illudens, and Isolation of Illudins S and M from the Fermentation Broth ofOmphalotus Olearis

Production of antibiotics by Collybia nivalis, Omphalotus olearis, a Favolaschia and a Pterula species on natural substrates.

Sesquiterpenes from Omphalotus illudens

Omphalotus olivascens

1 reference

Isolation of Illudin S from the Mushroom Omphalotus olivascens

Omphalotus guepiniformis

1 reference

Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro

subject has role

antineoplastic antibiotics

1 reference

Medical Subject Headings

MeSH descriptor ID

C008105

InChI=1S/C15H20O4/c1-8-10-9(6-13(2,7-16)12(10)18)11(17)14(3,19)15(8)4-5-15/h6,12,16,18-19H,4-5,7H2,1-3H3/t12-,13+,14+/m1/s1

15 March 2018

Identifiers

InChI

1 reference

Illudin S (English)

19 November 2016

2 references

Illudin S (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

1149-99-1

2 references

Global Substance Registration System

UNII

EWJ0GY2H7X

https://commonchemistry.cas.org/detail?cas_rn=1149-99-1

illudin s (English)

19 November 2016

6 April 2021

1 reference

Lampterol (English)

19 November 2016

2 references

English

title

Illudin S (English)

19 November 2016

ChEBI ID

5867

mapping relation type

2 references

English

title

ILLUDIN (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C15H20O4/c1-8-10-9(6-13(2,7-16)12(10)18)11(17)14(3,19)15(8)4-5-15/h6,12,16,18-19H,4-5,7H2,1-3H3/t12-,13+,14+/m1/s1

1 reference

ILLUDIN (English)

19 November 2016

2 references

inferred from InChIKey

1 reference

1 reference

0 references

0 references

1 reference

Medical Subject Headings

14 March 2018

1 reference

Global Substance Registration System

Illudin S (English)

5 October 2016

2 references

UNII

EWJ0GY2H7X

English

title

illudin s (English)

19 November 2016

Natural Product Atlas ID

NPA019033

2 references

based on heuristic

inferred from InChIKey

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

Illudin S (English)

5 October 2016

1 reference

30 June 2018

1 reference

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023