aphidicolin (Q414000)

MFCD00083214 (English)

20 September 2016

chemical formula

C₂₀H₃₄O₄

1 reference

MFCD00083214 (English)

20 September 2016

canonical SMILES

CC12CCC(C(C1CCC3C24CCC(C(C3)C4)(CO)O)(C)CO)O

1 reference

MFCD00083214 (English)

20 September 2016

isomeric SMILES

C[C@]12CC[C@H]([C@@]([C@@H]1CC[C@@H]3C24CC[C@@]([C@H](C3)C4)(CO)O)(C)CO)O

1 reference

MFCD00083214 (English)

20 September 2016

found in taxon

Pleospora bjoerlingii

6 references

3-Deoxyaphidicolin and aphidicolin analogues as phytotoxins from Phoma betae.

Biosynthesis of diterpenoid aphidicolin: Isolation of intermediates from P-450 inhibitor treated mycelia of Phoma betae

The later stage of the biosynthesis of aphidicolin: Accumulation of intermediates with cytochrome P-450 inhibitors.

Phytotoxicity of the new metabolites produced by Phoma betae, the cause of phoma root rot and leaf spot in sugar beet (Beta vulgaris L.).

3-Deoxyaphidicolin and Aphidi-colin Analogues as Phytotoxins fromPhoma betae

Biosynthesis of diterpenoid aphidicolin: Isolation of intermediates from P-450 inhibitor treated mycelia of Phoma betae

Cephalosporium aphidicola

12 references

Aphidicolane metabolites of Cephalosporium aphidicola

An oxygen-18 study of the biosynthesis of the diterpenoid, aphidicolin in cephalosporium aphidicola

The hydroxylation at C-17 in the biosynthesis of the diterpenoid aphidicolin

The late stages of the biosynthesis of the diterpenoid aphidicolin in Cephalosporium aphidicola

Studies in terpenoid biosynthesis. Part 30. The acetate and mevalonate labelling patterns of the diterpenoid, aphidicolin

The structure of thiobiscephalosporolide A, A dimeric pentaketide macrolide from Cephalosporium aphidicola

Studies in terpenoid biosynthesis. Part 32. The incorporation of aphidicolan-16-ene and aphidicolon-16β-ol into the diterpenoid aphidicolin by the fungus Cephalosporium aphidicola

Studies in terpenoid biosynthesis. Part 38. The role of an 16β,17-epoxyaphidicolane in the minor biosynthetic pathway leading to aphidicolin

Studies in terpenoid biosynthesis. Part 39. The stereochemistry of the relationship between substrate and oxidant in the hydroxylation of aphidicolin at C-18 by Cephalosporium aphidicola

The structure and absolute configuration of the antibiotic aphidicolin: a tetracyclic diterpenoid containing a new ring system

The structure of thiobiscephalosporolide A, A dimeric pentaketide macrolide from Cephalosporium aphidicola

Isolation and Characterization of Aphidicolin and Chlamydosporol Derivatives fromTolypocladium inflatum

Nigrospora oryzae

1 reference

The anti-promyelocytic leukemia mode of action of two endophytic secondary metabolites unveiled by a proteomic approach.

Nigrospora sphaerica

1 reference

The anti-promyelocytic leukemia mode of action of two endophytic secondary metabolites unveiled by a proteomic approach.

Tolypocladium inflatum

1 reference

Isolation and Characterization of Aphidicolin and Chlamydosporol Derivatives fromTolypocladium inflatum

Harziella entomophila

1 reference

Isolation of aphidicolin as a root growth inhibitor from Harziella entomophilla.

Botryotinia fuckeliana

1 reference

Aphidicolin Chemistry of the Deep-Sea-Derived Fungus Botryotinia fuckeliana MCCC 3A00494

Botrytis cinerea

1 reference

Aphidicolin Chemistry of the Deep-Sea-Derived Fungus Botryotinia fuckeliana MCCC 3A00494

Pyrenula

1 reference

Polyketides from the cultured lichen mycobiont of a Vietnamese Pyrenula sp.

subject has role

antiviral agent

1 reference

Medical Subject Headings

15 March 2018

1 reference

Medical Subject Headings

MeSH descriptor ID

D016590

InChI=1S/C20H34O4/c1-17(11-21)15-4-3-13-9-14-10-19(13,7-8-20(14,24)12-22)18(15,2)6-5-16(17)23/h13-16,21-24H,3-12H2,1-2H3/t13-,14+,15-,16+,17-,18-,19-,20-/m0/s1

15 March 2018

Identifiers

InChI

1 reference

aphidicolin (English)

NOFOAYPPHIUXJR-APNQCZIXSA-N

19 October 2016

InChIKey

2 references

aphidicolin (English)

19 October 2016

imported from Wikimedia project

ChEBI release 2020-09-01

CAS Registry Number

38966-21-1

2 references

German Wikipedia

InChIKey

NOFOAYPPHIUXJR-APNQCZIXSA-N

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=38966-21-1

1 reference

(2S,5R,6R,7R,10S,12R,13R)-6,13-Bis(hydroxymethyl)-2,6-dimethyltetracyclo[10.3.1.0~1,10~.0~2,7~]hexadecane-5,13-diol (English)

20 September 2016

1 reference

APHIDICOLIN (English)

19 October 2016

1 reference

aphidicolin (English)

19 October 2016

Reaxys registry number

4689958

1 reference

aphidicolin (English)

19 October 2016

2055641

1 reference

aphidicolin (English)

19 October 2016

ChEBI ID

2766

mapping relation type

exact match

1 reference

splash10-03di-0898000000-a44a30192db3c23b3313

ChEBI release 2019-10-02

SureChEMBL ID

SCHEMBL183956

1 reference

based on heuristic

inferred from InChIKey

1 reference

0 references

DSSTox substance ID

DTXSID5036711

0 references

DSSTOX compound identifier

0 references

0 references

609-602-3

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.109.656

27 December 2018

ECHA Substance Infocard ID

Aphidicolin from Nigrospora sphaerica (English)

quotation

CAS no.: 38966-21-1 (English)

100.109.656

1 reference

reference URL

http://echa.europa.eu/de/information-on-chemicals/registered-substances

MeSH descriptor ID

D016590

subject named as

Aphidicolin

0 references

0 references

1 reference

aphidicolin (English)

19 October 2016

1 reference

aphidicolin (English)

19 October 2016

UNII

192TJ6PP19

0 references

Natural Product Atlas ID

NPA010945

1 reference

based on heuristic

inferred from InChIKey

0 references

1 reference

https://docs.openalex.org/download-snapshot/snapshot-data-format

aphidicolin (English)

19 October 2016

0 references

0 references

1 reference

28 October 2013

Microsoft Academic ID

0 references

1 reference

26 January 2022

1 reference

4Q5V (English)