Introduction:Basic information about CAS 454-29-5|DL-Homocysteine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
DL-Homocysteine is a weak neurotoxin, and can affect the production of kynurenic acid in the brain.
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Target
Human Endogenous Metabolite
In Vitro
DL-Homocysteine (0.1-0.5 mM) significantly enhances kynurenic acid (KYNA) production in rat cortical slices, and diministes the production of at 3.0, 5.0, and 10.0 mM, with the estimated IC50 of 6.4 (5.5-7.5) mM. DL-Homocysteine dose-dependently inhibits kynurenine aminotransferases I (KATI) activity at concentrations ≥0.2 mM, with an IC50 of 0.566 (0.442-0.724) mM, and the activity of KAT II with IC50 value of 8.046 (5.804-11.154) mM[1].
In Vivo
DL-Homocysteine (1.3 mmol/kg, i.p.) increases KYNA content (pmol/g tissue) from 8.47 ± 1.57 to 13.04 ± 2.86 and 11.4 ± 1.72 in cortex, and from 4.11 ± 1.54 to 10.02 ± 3.08 in rat hippocampus[1].
References
[1]. DL-Homocysteine, et al. Dual effect of DL-homocysteine and S-adenosylhomocysteine on brain synthesis of the glutamate receptor antagonist, kynurenic acid. J Neurosci Res. 2005 Feb 1;79(3):375-82.
Chemical & Physical Properties
Density
1.3±0.1 g/cm3
Boiling Point
299.7±35.0 °C at 760 mmHg
Melting Point
232-233 °C(lit.)
Molecular Formula
C4H9NO2S
Molecular Weight
135.185
Flash Point
135.0±25.9 °C
Exact Mass
135.035400
PSA
102.12000
LogP
0.22
Vapour Pressure
0.0±1.3 mmHg at 25°C
Index of Refraction
1.538
InChIKey
FFFHZYDWPBMWHY-UHFFFAOYSA-N
SMILES
NC(CCS)C(=O)O
Storage condition
2-8°C
Stability
Stable. Combustible. Incompatible with strong oxidizing agents.
Toxicological Information
CHEMICAL IDENTIFICATION
RTECS NUMBER :
MT0175000
CHEMICAL NAME :
DL-Homocysteine
CAS REGISTRY NUMBER :
454-29-5
LAST UPDATED :
199709
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C4-H9-N-O2-S
MOLECULAR WEIGHT :
135.20
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
770 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
MUTATION DATA
TYPE OF TEST :
Phage inhibition capacity
TEST SYSTEM :
Bacteria - Escherichia coli
DOSE/DURATION :
125 mg/L
REFERENCE :
APMBAY Applied Microbiology. (Washington, DC) V.1-30, 1953-75. For publisher information, see AEMIDF. Volume(issue)/page/year: 12,234,1964
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