615609
Indole-2,4,5,6,7-d5-3-acetic-2,2-d2 acid
97 atom % D
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About This Item
Empirical Formula (Hill Notation):
C10D7H2NO2
Molecular Weight:
182.23
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
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isotopic purity
97 atom % D
form
solid
technique(s)
mass spectrometry (MS): suitable
mp
165-169 °C (lit.)
mass shift
M+7
SMILES string
[2H]c1[nH]c2c([2H])c([2H])c([2H])c([2H])c2c1C([2H])([2H])C(O)=O
InChI
1S/C10H9NO2/c12-10(13)5-7-6-11-9-4-2-1-3-8(7)9/h1-4,6,11H,5H2,(H,12,13)/i1D,2D,3D,4D,5D2,6D
InChI key
SEOVTRFCIGRIMH-PYNXLSDISA-N
Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Teresa Zelante et al.
Cell reports, 34(4), 108673-108673 (2021-01-28)
Indoleamine 2,3-dioxygenases (IDOs) degrade l-tryptophan to kynurenines and drive the de novo synthesis of nicotinamide adenine dinucleotide. Unsurprisingly, various invertebrates, vertebrates, and even fungi produce IDO. In mammals, IDO1 also serves as a homeostatic regulator, modulating immune response to infection
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