CHEBI:16345 - 3-sulfino-L-alanine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 3-sulfino-L-alanine
ChEBI ID CHEBI:16345
ChEBI ASCII Name 3-sulfino-L-alanine
Definition The organosulfinic acid arising from oxidation of the sulfhydryl group of L-cysteine.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:8973, CHEBI:21271, CHEBI:41618, CHEBI:11888, CHEBI:1664, CHEBI:11889
Supplier Information
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Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
metabotropic glutamate receptor agonist
An agonist that selectively binds to and activates a metabotropic glutamate receptor.
Related Structures
3-sulfino-L-alanine has Substituent Group(s)
3-sulfino-L-alanine residue
Mass : 135.143
Formula : C3H5NO3S
61967
3-sulfino-L-alanine is a Structural Derivative of
sulfinic acid
Mass : 66.08068
Formula : H2O2S
29213
oxoacid
Definition : A compound which contains oxygen, at least one other element, and at least one hydrogen bound to oxygen, and which produces a conjugate base by loss of positive hydrogen ion(s) (hydrons).
ammonia
Mass : 17.03056
Formula : H3N
16134
L-cysteine
Mass : 121.15800
Formula : C3H7NO2S
17561
cysteine
Mass : 121.15922
Formula : C3H7NO2S
15356
proteinogenic amino acid
Definition : Any of the 23 alpha-amino acids that are precursors to proteins, and are incorporated into proteins during translation. The group includes the 20 amino acids encoded by the nuclear genes of eukaryotes together with selenocysteine, pyrrolysine, and N-formylmethionine. Apart from glycine, which is non-chiral, all have L configuration.
3-sulfino-L-alanine is a Conjugate Acid of
3-sulfino-L-alanine(1-)
Mass : 152.14900
Formula : C3H6NO4S
61085
3-sulfino-L-alanine is a Tautomer of
L-cysteine-S-dioxide
Mass : 153.15700
Formula : C3H7NO4S
41721
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Relationship Types
is a
has part
is conjugate base of
is conjugate acid of
is tautomer of
is enantiomer of
has functional parent
has parent hydride
is substituent group from
has role
Status
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Unchecked