(Q63409819)

English

(12S)-6,15-dihydroxy-8,12,13,13-tetramethyl-4,11-dioxatetracyclo[7.6.1.05,16.010,14]hexadeca-1(15),5,7,9(16),10(14)-pentaene-2,3-dione

chemical compound

In more languages

default for all languages

No label defined

No description defined

edit

Statements

instance of

type of chemical entity

0 references

subclass of

6,15-dihydroxy-8,12,13,13-tetramethyl-4,11-dioxatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),5,7,9,14-pentaene-2,3-dione

1 reference

based on heuristic

inferred from SMILES

mass

328.094688232 dalton

1 reference

based on heuristic

inferred from isomeric SMILES

chemical formula

C₁₈H₁₆O₆

0 references

canonical SMILES

O=C1OC2=C(O)C=C(C=3C=4OC(C)C(C4C(O)=C(C1=O)C23)(C)C)C

0 references

isomeric SMILES

C[C@H]1C(C2=C(O1)C3=C4C(=C2O)C(=O)C(=O)OC4=C(C=C3C)O)(C)C

0 references

found in taxon

Sirococcus

1 reference

stated in

Sclerodin and related compounds from a plant disease causing fungus. Scleroderris yellow

Scleroderris canker

3 references

stated in

Metabolites produced by the scleroderris canker fungus, Gremmeniellaabietina. Part 2. The structure of scleroderolide

stated in

Metabolites produced by the Scleroderris canker fungus, Gremmeniellaabietina. Part 4. Biosynthetic studies

stated in

Metabolites produced by the scleroderris canker fungus, Gremmeniellaabietina. Part 2. The structure of scleroderolide

Massarina bipolaris

1 reference

stated in

Metabolites produced by the scleroderris canker fungus, Gremmeniellaabietina. Part 2. The structure of scleroderolide

Coniothyrium cereale

1 reference

stated in

Antimicrobial phenalenone derivatives from the marine-derived fungus Coniothyrium cereale

Coniothyrium cerealis

1 reference

stated in

Antimicrobial phenalenone derivatives from the marine-derived fungus Coniothyrium cereale

Neosetophoma cerealis

1 reference

stated in

Antimicrobial phenalenone derivatives from the marine-derived fungus Coniothyrium cereale

Penicillium

1 reference

stated in

Erabulenols, inhibitors of cholesteryl ester transfer protein produced by Penicillium sp. FO-5637. I.Production, isolation and biological properties

Identifiers

InChI

InChI=1S/C18H16O6/c1-6-5-8(19)15-10-9(6)16-12(18(3,4)7(2)23-16)13(20)11(10)14(21)17(22)24-15/h5,7,19-20H,1-4H3/t7-/m0/s1

0 references

InChIKey

MYDJDVOVZVSVIE-ZETCQYMHSA-N

0 references

0 references

1 reference

matched by identifier from

InChIKey

MYDJDVOVZVSVIE-ZETCQYMHSA-N

ChEBI ID

204068

mapping relation type

exact match

1 reference

matched by identifier from

International Chemical Identifier

InChI

InChI=1S/C18H16O6/c1-6-5-8(19)15-10-9(6)16-12(18(3,4)7(2)23-16)13(20)11(10)14(21)17(22)24-15/h5,7,19-20H,1-4H3/t7-/m0/s1

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

DSSTOX compound identifier

DTXCID301323197

0 references

Natural Product Atlas ID

NPA007117

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

InChIKey

MYDJDVOVZVSVIE-ZETCQYMHSA-N

NPA018063

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

InChIKey

MYDJDVOVZVSVIE-ZETCQYMHSA-N

(Q63409819)

(12S)-6,15-dihydroxy-8,12,13,13-tetramethyl-4,11-dioxatetracyclo[7.6.1.05,16.010,14]hexadeca-1(15),5,7,9(16),10(14)-pentaene-2,3-dione

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)