Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C55H87NO14 |
Molecular Weight | 986.2776 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 15 / 15 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@@H](C)[C@@](O)(O1)C(=O)C(=O)N3CCCC[C@@]3([H])C(=O)O[C@@H](CC(=O)[C@H](C)\C=C(C)\[C@@H](O)[C@@H](OC)C(=O)[C@H](C)C[C@H](C)\C=C\C=C\C=C(C)\[C@H](C2)OC)[C@H](C)C[C@@H]4CC[C@@H](OCCOCC)[C@@H](C4)OC
InChI
InChIKey=YYSFXUWWPNHNAZ-PKJQJFMNSA-N
InChI=1S/C55H87NO14/c1-12-67-26-27-68-45-24-22-41(31-48(45)65-10)30-37(5)47-33-44(57)36(4)29-39(7)50(59)51(66-11)49(58)38(6)28-34(2)18-14-13-15-19-35(3)46(64-9)32-42-23-21-40(8)55(63,70-42)52(60)53(61)56-25-17-16-20-43(56)54(62)69-47/h13-15,18-19,29,34,36-38,40-43,45-48,50-51,59,63H,12,16-17,20-28,30-33H2,1-11H3/b15-13+,18-14+,35-19+,39-29+/t34-,36-,37-,38-,40-,41+,42+,43+,45-,46+,47+,48-,50-,51+,55-/m1/s1
Umirolimus (Biolimus A9), an analogue of sirolimus, is a highly lipophilic macrolide compound developed by Biosensors International as an antiproliferative agent in coronary artery restenosis. Umirolimus has immunosuppressive and anti-inflammatory effects. It is used for the prevention of restenosis.
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Mixed agonist-antagonist properties of umespirone at neostriatal dopamine receptors in relation to its behavioral effects in the rat. | 1992 Nov 3 |
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Polymer-free Drug-Coated Coronary Stents in Patients at High Bleeding Risk. | 2015 Nov 19 |
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Comparison of Biolimus Versus Everolimus for Drug-Eluting Stents in the Percutaneous Treatment of Infra-Inguinal Arterial Disease. | 2017 |
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NCI_THESAURUS |
C574
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NCI_THESAURUS |
C2201
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SUB33179
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C152800
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U36PGF65JH
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100000126004
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U36PGF65JH
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UMIROLIMUS
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ACTIVE MOIETY