1.0 2016-05-25 18:25:21 UTC 2026-05-14 16:58:10 UTC Micafungin SmallMolecule Micafungin is a compound with the chemical formula C56H71N9O23S. Micafungin belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. With an average molecular weight of 1,270 g/mol, Micafungin is a heavy molecule. The compound is found in or released from two recorded sources: antennas in electrical and electronic equipment and antimycotics in healthcare, pharmaceuticals, and veterinary products. The recorded route of exposure for this substance is intravenous. Micafungin acts upon two recorded protein targets, serving as an inhibitor or modulator of 1,3-beta-glucan synthase component GSC2 and 1,3-beta-glucan synthase component FKS1 (fksA). C56H71N9O23S 1270.274 1269.438350313 {5-[(1S,2S)-2-[(3S,6S,9S,11R,15S,18S,20R,21R,24S,25S,26S)-3-[(1R)-2-carbamoyl-1-hydroxyethyl]-11,20,21,25-tetrahydroxy-15-[(1R)-1-hydroxyethyl]-26-methyl-2,5,8,14,17,23-hexaoxo-18-(4-{5-[4-(pentyloxy)phenyl]-1,2-oxazol-3-yl}benzamido)-1,4,7,13,16,22-hexaazatricyclo[22.3.0.0⁹,¹³]heptacosan-6-yl]-1,2-dihydroxyethyl]-2-hydroxyphenyl}oxidanesulfonic acid micafungin 235114-32-6 CCCCCOC1=CC=C(C=C1)C1=CC(=NO1)C1=CC=C(C=C1)C(=O)N[C@H]1C[C@@H](O)[C@@H](O)NC(=O)[C@@H]2[C@@H](O)[C@@H](C)CN2C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H](NC1=O)[C@@H](C)O)[C@H](O)[C@@H](O)C1=CC(OS(O)(=O)=O)=C(O)C=C1)[C@H](O)CC(N)=O InChI=1S/C56H71N9O23S/c1-4-5-6-17-86-32-14-11-28(12-15-32)39-21-33(63-87-39)27-7-9-29(10-8-27)49(75)58-34-20-38(70)52(78)62-54(80)45-46(72)25(2)23-65(45)56(82)43(37(69)22-41(57)71)60-53(79)44(48(74)47(73)30-13-16-36(68)40(18-30)88-89(83,84)85)61-51(77)35-19-31(67)24-64(35)55(81)42(26(3)66)59-50(34)76/h7-16,18,21,25-26,31,34-35,37-38,42-48,52,66-70,72-74,78H,4-6,17,19-20,22-24H2,1-3H3,(H2,57,71)(H,58,75)(H,59,76)(H,60,79)(H,61,77)(H,62,80)(H,83,84,85)/t25-,26+,31+,34-,35-,37+,38+,42-,43-,44-,45-,46-,47-,48-,52+/m0/s1 PIEUQSKUWLMALL-YABMTYFHSA-N Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Oligopeptides 1-hydroxy-2-unsubstituted benzenoids Alkanolamines Alkyl aryl ethers Aromatic alcohols Azacyclic compounds Benzamides Benzoyl derivatives Carbonyl compounds Cyclic peptides Fatty amides Heteroaromatic compounds Hydrocarbon derivatives Isoxazoles Lactams Macrolactams N-acyl-alpha amino acids and derivatives Organic oxides Organopnictogen compounds Oxacyclic compounds Phenol ethers Phenoxy compounds Phenylsulfates Polyols Primary carboxylic acid amides Pyrrolidines Secondary alcohols Secondary carboxylic acid amides Sulfuric acid monoesters Tertiary carboxylic acid amides 1-hydroxy-2-unsubstituted benzenoid Alcohol Alkanolamine Alkyl aryl ether Alpha-amino acid or derivatives Alpha-oligopeptide Aromatic alcohol Aromatic heteropolycyclic compound Arylsulfate Azacycle Azole Benzamide Benzenoid Benzoic acid or derivatives Benzoyl Carbonyl group Carboxamide group Cyclic alpha peptide Ether Fatty acyl Fatty amide Heteroaromatic compound Hydrocarbon derivative Isoxazole Lactam Macrolactam Monocyclic benzene moiety N-acyl-alpha amino acid or derivatives Organic nitrogen compound Organic oxide Organic oxygen compound Organic sulfuric acid or derivatives Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Oxacycle Phenol Phenol ether Phenoxy compound Phenylsulfate Polyol Primary carboxylic acid amide Pyrrolidine Secondary alcohol Secondary carboxylic acid amide Sulfate-ester Sulfuric acid ester Sulfuric acid monoester Tertiary carboxylic acid amide Aromatic heteropolycyclic compounds antibiotic antifungal drug echinocandin Detected and Not Quantified Micafungin Action Pathway SMP0126061 Micafungin Drug Metabolism Action Pathway SMP0143561 logp -6.3 logp 0.67 ALOGPS logs -3.77 ALOGPS solubility 2.18e-01 g/l ALOGPS logp -6.3 ChemAxon pka_strongest_acidic -2.2 ChemAxon pka_strongest_basic -3.6 ChemAxon iupac {5-[(1S,2S)-2-[(3S,6S,9S,11R,15S,18S,20R,21R,24S,25S,26S)-3-[(1R)-2-carbamoyl-1-hydroxyethyl]-11,20,21,25-tetrahydroxy-15-[(1R)-1-hydroxyethyl]-26-methyl-2,5,8,14,17,23-hexaoxo-18-(4-{5-[4-(pentyloxy)phenyl]-1,2-oxazol-3-yl}benzamido)-1,4,7,13,16,22-hexaazatricyclo[22.3.0.0⁹,¹³]heptacosan-6-yl]-1,2-dihydroxyethyl]-2-hydroxyphenyl}oxidanesulfonic acid ChemAxon average_mass 1270.274 ChemAxon mono_mass 1269.438350313 ChemAxon smiles CCCCCOC1=CC=C(C=C1)C1=CC(=NO1)C1=CC=C(C=C1)C(=O)N[C@H]1C[C@@H](O)[C@@H](O)NC(=O)[C@@H]2[C@@H](O)[C@@H](C)CN2C(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H](NC1=O)[C@@H](C)O)[C@H](O)[C@@H](O)C1=CC(OS(O)(=O)=O)=C(O)C=C1)[C@H](O)CC(N)=O ChemAxon formula C56H71N9O23S ChemAxon inchi InChI=1S/C56H71N9O23S/c1-4-5-6-17-86-32-14-11-28(12-15-32)39-21-33(63-87-39)27-7-9-29(10-8-27)49(75)58-34-20-38(70)52(78)62-54(80)45-46(72)25(2)23-65(45)56(82)43(37(69)22-41(57)71)60-53(79)44(48(74)47(73)30-13-16-36(68)40(18-30)88-89(83,84)85)61-51(77)35-19-31(67)24-64(35)55(81)42(26(3)66)59-50(34)76/h7-16,18,21,25-26,31,34-35,37-38,42-48,52,66-70,72-74,78H,4-6,17,19-20,22-24H2,1-3H3,(H2,57,71)(H,58,75)(H,59,76)(H,60,79)(H,61,77)(H,62,80)(H,83,84,85)/t25-,26+,31+,34-,35-,37+,38+,42-,43-,44-,45-,46-,47-,48-,52+/m0/s1 ChemAxon inchikey PIEUQSKUWLMALL-YABMTYFHSA-N ChemAxon polar_surface_area 510.14 ChemAxon refractivity 303.07 ChemAxon polarizability 128.22 ChemAxon rotatable_bond_count 18 ChemAxon acceptor_count 22 ChemAxon donor_count 16 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon #<HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f3bbfe521d8> DB01141 3081921 2339421 BE0004669 BE0010066