1.0 2010-04-08 22:10:26 UTC 2025-11-18 23:40:23 UTC FDB012935 Curvacin A Production by Lactobacillus curvatus LTH 1174. Bacteriocin. C23H35NOS 373.6 373.243935925 (4R)-4-[(1Z,5E,7E,11R)-11-methoxy-8-methyltetradeca-1,5,7,13-tetraen-1-yl]-2-[(1R,2S)-2-methylcyclopropyl]-4,5-dihydro-1,3-thiazole (4R)-4-[(1Z,5E,7E,11R)-11-methoxy-8-methyltetradeca-1,5,7,13-tetraen-1-yl]-2-[(1R,2S)-2-methylcyclopropyl]-4,5-dihydro-1,3-thiazole 146239-44-3 [H]\C(CC\C([H])=C(\[H])[C@]1([H])CSC(=N1)[C@]1([H])C[C@]1([H])C)=C(\[H])/C(/[H])=C(\C)CC[C@]([H])(CC=C)OC InChI=1S/C23H35NOS/c1-5-11-21(25-4)15-14-18(2)12-9-7-6-8-10-13-20-17-26-23(24-20)22-16-19(22)3/h5,7,9-10,12-13,19-22H,1,6,8,11,14-17H2,2-4H3/b9-7+,13-10-,18-12+/t19-,20+,21-,22+/m0/s1 LUEYTMPPCOCKBX-KWYHTCOPSA-N belongs to the class of organic compounds known as imidothiolactones. These are analogs of imidolactones where the oxygen atom is replaced by a sulfur atom. They have the general structure RC(=N)SR' where the central carbon atom is part of a ring. R,R' = organyl group. Imidothiolactones Organic compounds Organosulfur compounds Imidothioesters Imidothiolactones Aliphatic heteromonocyclic compounds Azacyclic compounds Dialkyl ethers Hydrocarbon derivatives Organonitrogen compounds Organopnictogen compounds Propargyl-type 1,3-dipolar organic compounds Thiazolines Aliphatic heteromonocyclic compound Azacycle Dialkyl ether Ether Hydrocarbon derivative Imidothiolactone Meta-thiazoline Organic 1,3-dipolar compound Organic nitrogen compound Organic oxygen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Propargyl-type 1,3-dipolar organic compound thiazoles logp 6.88 ALOGPS logs -6.71 ALOGPS solubility 7.30e-05 g/l ALOGPS logp 6.09 ChemAxon pka_strongest_basic 4.35 ChemAxon iupac (4R)-4-[(1Z,5E,7E,11R)-11-methoxy-8-methyltetradeca-1,5,7,13-tetraen-1-yl]-2-[(1R,2S)-2-methylcyclopropyl]-4,5-dihydro-1,3-thiazole ChemAxon average_mass 373.6 ChemAxon mono_mass 373.243935925 ChemAxon smiles [H]\C(CC\C([H])=C(\[H])[C@]1([H])CSC(=N1)[C@]1([H])C[C@]1([H])C)=C(\[H])/C(/[H])=C(\C)CC[C@]([H])(CC=C)OC ChemAxon formula C23H35NOS ChemAxon inchi InChI=1S/C23H35NOS/c1-5-11-21(25-4)15-14-18(2)12-9-7-6-8-10-13-20-17-26-23(24-20)22-16-19(22)3/h5,7,9-10,12-13,19-22H,1,6,8,11,14-17H2,2-4H3/b9-7+,13-10-,18-12+/t19-,20+,21-,22+/m0/s1 ChemAxon inchikey LUEYTMPPCOCKBX-KWYHTCOPSA-N ChemAxon polar_surface_area 21.59 ChemAxon refractivity 118.94 ChemAxon polarizability 45.54 ChemAxon rotatable_bond_count 12 ChemAxon acceptor_count 2 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 83478 Specdb::MsMs 83479 Specdb::MsMs 83480 Specdb::MsMs 145077 Specdb::MsMs 145078 Specdb::MsMs 145079 Specdb::MsMs 3220960 Specdb::MsMs 3220961 Specdb::MsMs 3220962 Specdb::MsMs 3605467 Specdb::MsMs 3605468 Specdb::MsMs 3605469