(Q105253220)

English

(1R,2S)-2,6,7,7-tetramethyltricyclo[6.2.1.01,5]undec-5-en-4-one

group of stereoisomers with the chemical formula C₁₅H₂₂O

In more languages

Statements

group of stereoisomers

0 references

1 reference

218.167065324 dalton

1 reference

based on heuristic

inferred from isomeric SMILES

chemical formula

C₁₅H₂₂O

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canonical SMILES

O=C1C2=C(C)C(C)(C)C3CCC2(C3)C(C)C1

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isomeric SMILES

CC1=C2C(=O)C[C@H](C)[C@]23CCC(C3)C1(C)C

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Streptomyces coelicolor

5 references

Streptomyces coelicolor as an expression host for heterologous gene clusters.

An orphan histidine kinase, OhkA, regulates both secondary metabolism and morphological differentiation in Streptomyces coelicolor

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

Secondary Metabolites Produced during the Germination of Streptomyces coelicolor.

Streptomyces thermocarboxydus

1 reference

Production of distinct labdane-type diterpenoids using a novel cryptic labdane-like cluster from Streptomyces thermocarboxydus K155

Streptomyces nodosus

1 reference

Exploiting the genome sequence of Streptomyces nodosus for enhanced antibiotic production.

Streptomyces collinus

1 reference

Identification and activation of novel biosynthetic gene clusters by genome mining in the kirromycin producer Streptomyces collinus Tü 365.

Streptomyces spectabilis

1 reference

The complete genomic sequence of Streptomyces spectabilis NRRL-2792 and identification of secondary metabolite biosynthetic gene clusters

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

5 references

Secondary Metabolites Produced during the Germination of Streptomyces coelicolor.

Streptomyces coelicolor as an expression host for heterologous gene clusters.

An orphan histidine kinase, OhkA, regulates both secondary metabolism and morphological differentiation in Streptomyces coelicolor

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

Identifiers

InChI=1S/C15H22O/c1-9-7-12(16)13-10(2)14(3,4)11-5-6-15(9,13)8-11/h9,11H,5-8H2,1-4H3/t9-,11?,15+/m0/s1

0 references

SHUZZAXJEJPUGA-YSTXANQKSA-N

0 references

1 reference

17 September 2022

based on heuristic

inferred from InChIKey

1 reference

SHUZZAXJEJPUGA-YSTXANQKSA-N

17 April 2021

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

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