(Q104972396)

English

(1R,2S)-2,6,7,7-tetramethyltricyclo[6.2.1.01,5]undec-5-ene

group of stereoisomers with the chemical formula C₁₅H₂₄

In more languages

Statements

group of stereoisomers

0 references

1 reference

biogenic aliphatic hydrocarbon

1 reference

biogenic aliphatic hydrocarbon

204.187800768 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₁₅H₂₄

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canonical SMILES

C1(=C2CCC(C)C23CCC(C3)C1(C)C)C

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isomeric SMILES

CC1=C2CC[C@H](C)[C@]23CCC(C3)C1(C)C

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Streptomyces coelicolor

3 references

Exploitation of the Streptomyces coelicolor A3(2) genome sequence for discovery of new natural products and biosynthetic pathways

Biosynthesis of the sesquiterpene antibiotic albaflavenone in Streptomyces coelicolor A3(2)

Biosynthesis of the sesquiterpene antibiotic albaflavenone in Streptomyces coelicolor. Mechanism and stereochemistry of the enzymatic formation of epi-isozizaene

Streptomyces avermitilis

1 reference

Characterization of a silent sesquiterpenoid biosynthetic pathway in Streptomyces avermitilis controlling epi-isozizaene albaflavenone biosynthesis and isolation of a new oxidized epi-isozizaene metabolite.

Streptomyces albidoflavus

3 references

Exploitation of the Streptomyces coelicolor A3(2) genome sequence for discovery of new natural products and biosynthetic pathways

Biosynthesis of the sesquiterpene antibiotic albaflavenone in Streptomyces coelicolor. Mechanism and stereochemistry of the enzymatic formation of epi-isozizaene

Biosynthesis of the sesquiterpene antibiotic albaflavenone in Streptomyces coelicolor A3(2)

Identifiers

InChI=1S/C15H24/c1-10-5-6-13-11(2)14(3,4)12-7-8-15(10,13)9-12/h10,12H,5-9H2,1-4H3/t10-,12?,15+/m0/s1

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CYLSPJUZBPWJGC-PJRDJYAKSA-N

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2 references

17 September 2022

based on heuristic

inferred from InChIKey

matched by identifier from

CYLSPJUZBPWJGC-PJRDJYAKSA-N

1 reference

CYLSPJUZBPWJGC-PJRDJYAKSA-N

17 April 2021

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

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