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سیرولیموس

Structure via PubChem · Public domain (PubChem)

EntityQ32089· pop 32· linked from 698 articles

سیرولیموس

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Also known as rapamycin, WY-090217, AY-22989, (-)-rapamycin

دارو

Key facts

Drug.IUPAC_name
(1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-12-[(2R)-1-((1S,3R,4R)-4-hydroxy-3-methoxycyclohexyl)-2-propanyl]-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone
Drug.C
51
Drug.H
79
Drug.N
1
Drug.O
13
Drug.SMILES
O[C@@H]1CC[C@H](C[C@H]1OC)C[C@@H](C)[C@@H]4CC(=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](OC)C[C@@H]2CC[C@@H](C)[C@@](O)(O2)C(=O)C(=O)N3CCCC[C@H]3C(=O)O4
Drug.StdInChI
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
Drug.StdInChIKey
QFJCIRLUMZQUOT-HPLJOQBZSA-N
Drug.solubility
0.0026
Drug.Watchedfields
changed
Drug.verifiedrevid
732542693
Drug.image
Sirolimus structure.svg
Drug.image_class
skin-invert-image
Drug.width
250
Drug.image2
Sirolimus-from-1C9H-3D-sticks.png
Drug.image_class2
bg-transparent
Drug.width2
250
Drug.tradename
Rapamune, others

via Wikipedia infobox

Chemical data

Formula
C51H79NO13
Molecular weight
914.2 g/mol
IUPAC name
(1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-12-[(2R)-1-[(1S,3R,4R)-4-hydroxy-3-methoxycyclohexyl]propan-2-yl]-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone
SMILES
C[C@@H]1CC[C@H]2C[C@@H](/C(=C/C=C/C=C/[C@H](C[C@H](C(=O)[C@@H]([C@@H](/C(=C/[C@H](C(=O)C[C@H](OC(=O)[C@@H]3CCCCN3C(=O)C(=O)[C@@]1(O2)O)[C@H](C)C[C@@H]4CC[C@H]([C@@H](C4)OC)O)C)/C)O)OC)C)C)/C)OC
InChIKey
QFJCIRLUMZQUOT-HPLJOQBZSA-N
XLogP
6
Polar surface area
195 Ų
H-bond donors
3
H-bond acceptors
13
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Approved
Molecule type
Small molecule
First approval
1999
Admin. routes
oral, parenteral, topical
Indications
acute lymphoblastic leukemia, kidney disease, Abnormality of the cardiovascular system, acute graft vs. host disease

via ChEMBL · EBI

Research

28,544 papers

via PubMed

Described at

Link to a page describing this subject · not written by Vinony

Wikidata facts

Has part
carbon
Mass
913.555142
Show 14 more facts
Commons category
Sirolimus
chemical formula
C₅₁H₇₉NO₁₃
NCI Thesaurus ID
C1212
World Health Organisation international non-proprietary name
sirolimusum
canonical SMILES
CC1CCC2CC(C(=CC=CC=CC(CC(C(=O)C(C(C(=CC(C(=O)CC(OC(=O)C3CCCCN3C(=O)C(=O)C1(O2)O)C(C)CC4CCC(C(C4)OC)O)C)C)O)OC)C)C)C)OC
isomeric SMILES
CO[C@@H]1C[C@H](C[C@@H](C)[C@@H]2CC(=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](C[C@@H]3CC[C@@H](C)[C@@](O)(O3)C(=O)C(=O)N4CCCC[C@H]4C(=O)O2)OC)CC[C@H]1O
medical condition treated
graft-versus-host disease
route of administration
intravenous infusion and defusion
defined daily dose
3
subject has role
bactericide
found in taxon
Ophiocordyceps
legal status (medicine)
boxed warning
significant drug interaction
ketoconazole
Sources (8)

via Wikidata · CC0

Gallery (5)