(Q105126707)

English

(2S)-2-butyl-11-{[(Z,5Z)-4-methoxy-1H-[2,2'-bipyrrolyliden]-5-ylidene]methyl}-10-azabicyclo[7.2.1]dodeca-1(11),9(12)-diene

chemical compound

In more languages

Statements

type of chemical entity

0 references

2-butyl-11-{[(Z,5Z)-4-methoxy-1H-[2,2'-bipyrrolyliden]-5-ylidene]methyl}-10-azabicyclo[7.2.1]dodeca-1(11),9(12)-diene

1 reference

based on heuristic

inferred from SMILES

391.262362676 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₂₅H₃₃N₃O

0 references

canonical SMILES

N1=CC=CC1=C2C=C(OC)C(=CC=3NC4=CC3C(CCCC)CCCCCC4)N2

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isomeric SMILES

CCCC[C@H]1CCCCCCc2cc1c(/C=c1\[nH]/c(=C3/C=CC=N3)cc1OC)[nH]2

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Streptomyces spectabilis

1 reference

Potent in vitro antimalarial activity of metacycloprodigiosin isolated from Streptomyces spectabilis BCC 4785

Streptomyces coelicolor

2 references

The MtrAB two-component system controls antibiotic production in Streptomyces coelicolor A3(2).

Metabolic engineering of Streptomyces coelicolor for enhanced prodigiosins (RED) production.

Streptomyces lividans

1 reference

Characterization and localization of prodiginines from Streptomyces lividans suppressing Verticillium dahliae in the absence or presence of Arabidopsis thaliana

Streptomyces albidoflavus

2 references

The MtrAB two-component system controls antibiotic production in Streptomyces coelicolor A3(2).

Metabolic engineering of Streptomyces coelicolor for enhanced prodigiosins (RED) production.

Identifiers

InChI=1S/C25H33N3O/c1-3-4-10-18-11-7-5-6-8-12-19-15-20(18)22(27-19)16-24-25(29-2)17-23(28-24)21-13-9-14-26-21/h9,13-18,27-28H,3-8,10-12H2,1-2H3/b23-21-,24-16-/t18-/m0/s1

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JFJGSGABCGVJGJ-KIZPIYQRSA-N

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1 reference

17 September 2022

based on heuristic

inferred from InChIKey

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