1.0 2016-09-30 22:35:16 UTC 2020-04-22 15:04:55 UTC BMDB0000709 BMDB00709 L-Cysteinylglycine disulfide L-Cysteinylglycine disulphide (R)-N-(3-((2-Amino-2-carboxyethyl)dithio)-ala)-gly 3-[[2-Amino-2-[(carboxymethyl)carbamoyl]ethyl]dithio]-alanine Cystinyl-gly Cystinylglycine L-Cysteinyl-glycine disulfide (2R)-2-Amino-3-({2-amino-2-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl}disulfanyl)propanoate (2R)-2-Amino-3-({2-amino-2-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl}disulphanyl)propanoate (2R)-2-Amino-3-({2-amino-2-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl}disulphanyl)propanoic acid C8H15N3O5S2 297.352 297.045311985 (2R)-2-amino-3-({2-amino-2-[(carboxymethyl)carbamoyl]ethyl}disulfanyl)propanoic acid (2R)-2-amino-3-{[2-amino-2-(carboxymethylcarbamoyl)ethyl]disulfanyl}propanoic acid 70555-24-7 N[C@@H](CSSCC(N)C(=O)NCC(O)=O)C(O)=O InChI=1S/C8H15N3O5S2/c9-4(7(14)11-1-6(12)13)2-17-18-3-5(10)8(15)16/h4-5H,1-3,9-10H2,(H,11,14)(H,12,13)(H,15,16)/t4?,5-/m0/s1 ZHRLECIZINSPKL-AKGZTFGVSA-N belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Dipeptides Alpha amino acid amides Amino acids Carbonyl compounds Carboxylic acids Dialkyldisulfides Dicarboxylic acids and derivatives Hydrocarbon derivatives L-alpha-amino acids L-cysteine-S-conjugates Monoalkylamines N-acyl-alpha amino acids Organic oxides Organopnictogen compounds Secondary carboxylic acid amides Sulfenyl compounds Aliphatic acyclic compound Alpha-amino acid Alpha-amino acid amide Alpha-amino acid or derivatives Alpha-dipeptide Amine Amino acid Amino acid or derivatives Carbonyl group Carboxamide group Carboxylic acid Cysteine or derivatives Dialkyldisulfide Dicarboxylic acid or derivatives Hydrocarbon derivative L-alpha-amino acid L-cysteine-s-conjugate N-acyl-alpha amino acid or derivatives N-acyl-alpha-amino acid Organic disulfide Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Organosulfur compound Primary aliphatic amine Primary amine Secondary carboxylic acid amide Sulfenyl compound Aliphatic acyclic compounds Solid logp -3.97 ALOGPS logs -1.66 ALOGPS logp -7 ChemAxon pka_strongest_acidic 1.87 ChemAxon pka_strongest_basic 9.08 ChemAxon iupac (2R)-2-amino-3-({2-amino-2-[(carboxymethyl)carbamoyl]ethyl}disulfanyl)propanoic acid ChemAxon average_mass 297.352 ChemAxon mono_mass 297.045311985 ChemAxon smiles N[C@@H](CSSCC(N)C(=O)NCC(O)=O)C(O)=O ChemAxon formula C8H15N3O5S2 ChemAxon inchi InChI=1S/C8H15N3O5S2/c9-4(7(14)11-1-6(12)13)2-17-18-3-5(10)8(15)16/h4-5H,1-3,9-10H2,(H,11,14)(H,12,13)(H,15,16)/t4?,5-/m0/s1 ChemAxon inchikey ZHRLECIZINSPKL-AKGZTFGVSA-N ChemAxon polar_surface_area 155.74 ChemAxon refractivity 67.68 ChemAxon polarizability 28.47 ChemAxon rotatable_bond_count 9 ChemAxon acceptor_count 7 ChemAxon donor_count 5 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon number_of_rings 0 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::MsMs 312295 Specdb::MsMs 312296 Specdb::MsMs 312297 Specdb::MsMs 357520 Specdb::MsMs 357521 Specdb::MsMs 357522 Specdb::MsMs 2449192 Specdb::MsMs 2449193 Specdb::MsMs 2449194 Specdb::MsMs 2487051 Specdb::MsMs 2487052 Specdb::MsMs 2487053 Specdb::CMs 20785 Specdb::CMs 37709 Specdb::CMs 171618 Specdb::CMs 1072619 Specdb::CMs 1072621 Specdb::CMs 1072623 Specdb::CMs 1072625 Specdb::CMs 1072627 Specdb::CMs 1072629 Specdb::CMs 1072631 Specdb::CMs 1072633 Specdb::CMs 1072635 Specdb::CMs 1072637 Specdb::CMs 1072638 Specdb::CMs 1072640 Specdb::CMs 1072642 Specdb::CMs 1072643 Specdb::CMs 1072644 Specdb::CMs 1072646 Specdb::CMs 1072648 Specdb::CMs 1072650 Specdb::CMs 1072652 Specdb::CMs 1072654 Specdb::CMs 1072656 Specdb::CMs 1072658 Specdb::NmrOneD 145030 Specdb::NmrOneD 145031 Specdb::NmrOneD 145032 Specdb::NmrOneD 145033 Specdb::NmrOneD 145034 Specdb::NmrOneD 145035 Specdb::NmrOneD 145036 Specdb::NmrOneD 145037 Specdb::NmrOneD 145038 Specdb::NmrOneD 145039 Specdb::NmrOneD 145040 Specdb::NmrOneD 145041 Specdb::NmrOneD 145042 Specdb::NmrOneD 145043 Specdb::NmrOneD 145044 Specdb::NmrOneD 145045 Specdb::NmrOneD 145046 Specdb::NmrOneD 145047 Specdb::NmrOneD 145048 Specdb::NmrOneD 145049 FDB022195 17215992 89930 22833544 5677 Weygand, Friedrich; Zumach, Gerhard. Synthesis of cystine peptides by dehydrogenation with vicinal dihalogen derivatives. Zeitschrift fuer Naturforschung (1962), 17b 807-10. CODEN: ZNTFA2 ISSN:0372-9516. CAN 59:3854 AN 1963:403854