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[1. A compound derived from biotin by the removal of the sulfur atom; a precursor of biotin in bacteria and molds; it can substitute for biotin in some microorganisms, but is without effect on or is inhibitory to the growth of others.
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pre_formula( "InChI=1/C10H18N2O3/c1-7-8(12-10(15)11-7)5-3-2-4-6-9(13)14/h7-8H,2-6H2,1H3,(H,13,14)(H2,11,12,15)/t7-,8+/m0/s1/f/h11-13H", "jqp031/445027.html" ); ?>
Molecular Formula:
C10H18N2O3
InChI: InChI=1/C10H18N2O3/c1-7-8(12-10(15)11-7)5-3-2-4-6-9(13)14/h7-8H,2-6H2,1H3,(H,13,14)(H2,11,12,15)/t7-,8+/m0/s1/f/h11-13H
InChIKey: InChIKey=AUTOLBMXDDTRRT-RQTZSDEGDO
SMILES: C[C@@H]1NC(=O)N[C@@H]1CCCCCC(O)=O
CAS number 533-48-2
Names:
desthiobiotin
d-dethiobiotin
(+)-dethiobiotin
(4R,5S)-dethiobiotin
(4R,5S)-5-methyl-2-oxo-4-imidazolidinehexanoic acid
(4R-cis)-5-methyl-2-oxo-4-imidazolidinehexanoic acid
6-[(4R,5S)-5-methyl-2-oxo-imidazolidin-4-yl]hexanoic acid
name_it( "InChI=1/C10H18N2O3/c1-7-8(12-10(15)11-7)5-3-2-4-6-9(13)14/h7-8H,2-6H2,1H3,(H,13,14)(H2,11,12,15)/t7-,8+/m0/s1/f/h11-13H", "jqp031/445027.html" ); ?>
Registries:
pre_registry_key( "InChI=1/C10H18N2O3/c1-7-8(12-10(15)11-7)5-3-2-4-6-9(13)14/h7-8H,2-6H2,1H3,(H,13,14)(H2,11,12,15)/t7-,8+/m0/s1/f/h11-13H", "InChIKey=AUTOLBMXDDTRRT-RQTZSDEGDO", "jqp031/445027.html" ); ?>
PubChem CID 445027
Beilstein =84958
CAS 533-48-2 (from NIST)
ChEBI 36990
PubChem ID 10299620
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