Details
Stereochemistry | RACEMIC |
Molecular Formula | C6H12N2O4S |
Molecular Weight | 208.235 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@@H](CSC[C@H](N)C(O)=O)C(O)=O
InChI
InChIKey=DWPCPZJAHOETAG-IMJSIDKUSA-N
InChI=1S/C6H12N2O4S/c7-3(5(9)10)1-13-2-4(8)6(11)12/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12)/t3-,4-/m0/s1
Molecular Formula | C6H12N2O4S |
Molecular Weight | 208.235 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Synthesis of the lantibiotic lactocin S using peptide cyclizations on solid phase. | 2010 Jan 20 |
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New insights into the metabolism of organomercury compounds: mercury-containing cysteine S-conjugates are substrates of human glutamine transaminase K and potent inactivators of cystathionine γ-lyase. | 2012 Jan 1 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:58:46 GMT 2023
by
admin
on
Sat Dec 16 01:58:46 GMT 2023
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Record UNII |
9N5M8Q1P1C
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Record Status |
Validated (UNII)
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Record Version |
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98504
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9N5M8Q1P1C
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3183-08-2
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DTXSID601020926
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221-676-5
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m6686
Created by
admin on Sat Dec 16 01:58:46 GMT 2023 , Edited by admin on Sat Dec 16 01:58:46 GMT 2023
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PRIMARY | Merck Index |