Mureidomycin F

AlkaPlorer ID: AK032447

Synonym: 'Mureidomycin F'

IUPAC Name: 2-[[(2S)-1-[[2-amino-3-[(6-hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-methylamino]butanoyl]-[(E)-[5-(2,4-dioxopyrimidin-1-yl)-4-hydroxyoxolan-2-ylidene]methyl]amino]-4-methylsulfanyl-1-oxobutan-2-yl]carbamoylamino]-3-(3-hydroxyphenyl)propanoic acid

Structure

SMILES: CSCC[C@H](N=C(O)NC(CC1=CC=CC(O)=C1)C(=O)O)C(=O)N(/C=C1\CC(O)C(N2C=CC(O)=NC2=O)O1)C(=O)C(N)C(C)N(C)C(=O)C1CC2=CC(O)=CC=C2CN1

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InChI: InChI=1S/C39H48N8O12S/c1-20(45(2)33(52)28-16-23-15-25(49)8-7-22(23)18-41-28)32(40)35(54)47(19-26-17-30(50)36(59-26)46-11-9-31(51)44-39(46)58)34(53)27(10-12-60-3)42-38(57)43-29(37(55)56)14-21-5-4-6-24(48)13-21/h4-9,11,13,15,19-20,27-30,32,36,41,48-50H,10,12,14,16-18,40H2,1-3H3,(H,55,56)(H2,42,43,57)(H,44,51,58)/b26-19+/t20?,27-,28?,29?,30?,32?,36?/m0/s1

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InChIKey: AUSWKQLLJQGJQP-RMKGNSTMSA-N

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Properties Information

Molecule Weight: 852.9239999999999

TPSA: 302.7

MolLogP: 0.0464000000000062

Number of H-Donors: 9

Number of H-Acceptors: 16

RingCount: 5

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi

Metabolism Information