Showing Metabocard for S-(5-deoxy-D-ribos-5-yl)-L-homocysteine (BASm0003276)
| Common Name | S-(5-deoxy-d-ribos-5-yl)-l-homocysteine |
|---|---|
| Description | S-ribosyl-L-homocysteine is a member of the chemical class known as Alpha Amino Acids and Derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). AI-2 is spontaneously derived from 4,5-dihydroxy-2,3-pentanedione that, along with homocysteine, is produced by cleavage of S-adenosylhomocysteine (SAH) and S-ribosylhomocysteine by the Pfs and LuxS enzymes. (PMID 16885435 ) |
| Structure | |
| Molecular Formula | C9H17NO6S |
| Average Mass | 267.29900 |
| Monoisotopic Mass | 267.07766 |
| IUPAC Name | Not Available |
| Traditional Name | Not Available |
| CAS Registry Number | 15912-98-8 |
| SMILES | [NH3+][C@@H](CCSC[C@H]1OC(O)[C@H](O)[C@@H]1O)C(=O)[O-] |
| InChI Identifier | InChI=1S/C9H17NO6S/c10-4(8(13)14)1-2-17-3-5-6(11)7(12)9(15)16-5/h4-7,9,11-12,15H,1-3,10H2,(H,13,14)/t4-,5+,6+,7+,9?/m0/s1 |
| InChI Key | IQFWYNFDWRYSRA-BLELIYKESA-N |
| CHEBI ID | CHEBI:58195 |
| MiMeDB ID | MMDBc0030093 |
| State | Expected Solid |
| Water Solubility | Not Available |
| logS | Not Available |
| pKa (Strongest Acidic) | Not Available |
| pKa (Strongest Basic) | Not Available |
| Hydrogen Acceptor Count | Not Available |
| Hydrogen Donor Count | Not Available |
| Rotatable Bond Count | Not Available |
| Physiological Charge | Not Available |
| Formal Charge | Not Available |
| Polarizability | Not Available |