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RAPA;RAPAMYCIN
SpectraBase Compound ID 5sOB2NgH56w
InChI InChI=1S/C51H79NO13/c1-30-16-12-11-13-17-31(2)42(61-8)28-38-21-19-36(7)51(60,65-38)48(57)49(58)52-23-15-14-18-39(52)50(59)64-43(33(4)26-37-20-22-40(53)44(27-37)62-9)29-41(54)32(3)25-35(6)46(56)47(63-10)45(55)34(5)24-30/h11-13,16-17,25,30,32-34,36-40,42-44,46-47,53,56,60H,14-15,18-24,26-29H2,1-10H3/b13-11+,16-12+,31-17+,35-25+/t30-,32-,33-,34-,36-,37+,38+,39+,40-,42+,43+,44-,46-,47+,51-/m1/s1
InChIKey QFJCIRLUMZQUOT-HPLJOQBZSA-N
Mol Weight 914.2 g/mol
Molecular Formula C51H79NO13
Exact Mass 913.555142 g/mol
Enantiomer InChIKey QFJCIRLUMZQUOT-NFYPJHAMSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • RAPAMYCIN
Title Journal or Book Year
Selective Substitution of 31/42–OH in Rapamycin Guided by an in Situ IR Technique Molecules 2014
Selective Epimerization of Rapamycin via a Retroaldol/Aldol Mechanism Mediated by Titanium Tetraisopropoxide Organic Letters 1999
Incorporation of Acetate, Propionate, and Methionine into Rapamycin by Streptomyces hygroscopicus Journal of Natural Products 1991

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