Rapamycin-d3 (contains d0) Technical Grade

For research use only. Not for therapeutic Use.

  • CAT Number: R006524
  • CAS Number: 392711-19-2
  • Molecular Formula: C51H76D3NO13
  • Molecular Weight: 917.2
  • Purity: ≥95%
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Rapamycin-d3 is a deuterated form of rapamycin, a potent immunosuppressant and inhibitor of the mTOR (mechanistic target of rapamycin) pathway. The incorporation of three deuterium atoms into rapamycin enhances its stability and facilitates more accurate tracking in mass spectrometry and NMR studies. This isotopic labeling is useful in pharmacokinetic and pharmacodynamic studies, allowing researchers to monitor drug metabolism, distribution, and interactions within biological systems with greater precision. Rapamycin-d3 is employed in pharmaceutical research to optimize therapeutic strategies and investigate the effects of mTOR inhibition on cellular processes.


Catalog Number R006524
CAS Number 392711-19-2
Synonyms

(-)-Rapamycin-d3; AY 22989-d3; Antibiotic AY 22989-d3; Cypher-d3; NSC 226080-d3; RAPA-d3; RPM-d3; Rapammune-d3; Rapamune-d3; SIIA 9268A-d3; Sirolimus-d3; Wy 090217-d3;

Molecular Formula C51H76D3NO13
Purity ≥95%
Target Immunology/Inflammation
Storage -20°C
IUPAC Name (1R,9S,12S,15R,16Z,18R,19R,21R,23S,24Z,26Z,28Z,30S,32S,35R)-1,18-dihydroxy-12-[(2R)-1-[(1S,3R,4R)-4-hydroxy-3-methoxycyclohexyl]propan-2-yl]-19-methoxy-15,17,21,23,29,35-hexamethyl-30-(trideuteriomethoxy)-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone
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/i8D3
InChIKey QFJCIRLUMZQUOT-NWORAYHKSA-N
SMILES [2H]C([2H])([2H])O[C@H]\1C[C@@H]2CC[C@H]([C@@](O2)(C(=O)C(=O)N3CCCC[C@H]3C(=O)O[C@@H](CC(=O)[C@@H](/C=C(/[C@H]([C@H](C(=O)[C@@H](C[C@@H](/C=C/C=C/C=C1\C)C)C)OC)O)\C)C)[C@H](C)C[C@@H]4CC[C@H]([C@@H](C4)OC)O)O)C

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