Antibiotic SS 288B; 1,3C,3E,3F-Tetradeoxy 

AlkaPlorer ID: AK288713

Synonym: Cosmomycin C, β-Rhodomycin S2, 3B-Hydroxycytorhodin A, A 447B, A 262-2, Antibiotic A 447B, Antibiotic A 262-2, Cytorhodin O 

IUPAC Name: 7-[4-(dimethylamino)-5-[4-hydroxy-5-(5-hydroxy-6-methyloxan-2-yl)oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10-[4-(dimethylamino)-5-[5-(5-hydroxy-6-methyloxan-2-yl)oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-9-ethyl-4,6,9,11-tetrahydroxy-8,10-dihydro-7H-tetracene-5,12-dione

Structure

SMILES: CCC1(O)CC(OC2CC(N(C)C)C(OC3CC(O)C(OC4CCC(O)C(C)O4)C(C)O3)C(C)O2)C2=C(O)C3=C(C(=O)C4=CC=CC(O)=C4C3=O)C(O)=C2C1OC1CC(N(C)C)C(OC2CCC(OC3CCC(O)C(C)O3)C(C)O2)C(C)O1

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InChI: InChI=1S/C60H88N2O21/c1-12-60(71)25-40(79-44-22-33(61(8)9)57(30(6)75-44)82-46-24-38(66)58(31(7)77-46)81-42-20-17-36(64)27(3)73-42)48-51(55(70)49-50(54(48)69)53(68)47-32(52(49)67)14-13-15-37(47)65)59(60)83-45-23-34(62(10)11)56(29(5)76-45)80-43-21-18-39(28(4)74-43)78-41-19-16-35(63)26(2)72-41/h13-15,26-31,33-36,38-46,56-59,63-66,69-71H,12,16-25H2,1-11H3

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InChIKey: JRCMJKKALYUURJ-UHFFFAOYSA-N

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Properties Information

Molecule Weight: 1173.3569999999995

TPSA: 292.99

MolLogP: 4.702600000000007

Number of H-Donors: 7

Number of H-Acceptors: 23

RingCount: 10

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi

Metabolism Information