Homobatrachotoxine
composé chimique
From Wikipedia, the free encyclopedia
L'homobatrachotoxine est un alcaloïde stéroïdien.
SMILES
C1=2[C@@]3([C@@]4([C@@H](C[C@](O3)(O)CC4)CC2)C)[C@@H](C[C@@]23[C@@]1(CC=C2[C@@H](OC(c1c([nH]cc1C)CC)=O)C)OCC[N@@](C3)C)O
,
,
InChI
InChI :
InChI=1/C32H44N2O6/c1-6-23-26(19(2)17-33-23)27(36)39-20(3)22-9-10-31-24-8-7-21-15-30(37)12-11-28(21,4)32(24,40-30)25(35)16-29(22,31)18-34(5)13-14-38-31/h8-9,17,20-21,25,33,35,37H,6-7,10-16,18H2,1-5H3/t20?,21-,25-,28+,29?,30+,31+,32?/m1/s1
InChI=1/C32H44N2O6/c1-6-23-26(19(2)17-33-23)27(36)39-20(3)22-9-10-31-24-8-7-21-15-30(37)12-11-28(21,4)32(24,40-30)25(35)16-29(22,31)18-34(5)13-14-38-31/h8-9,17,20-21,25,33,35,37H,6-7,10-16,18H2,1-5H3/t20?,21-,25-,28+,29?,30+,31+,32?/m1/s1
| Homoatrachotoxine | ||
| Structure de l'homobatrachotoxine. | ||
| Identification | ||
|---|---|---|
| No CAS | ||
| SMILES | C1=2[C@@]3([C@@]4([C@@H](C[C@](O3)(O)CC4)CC2)C)[C@@H](C[C@@]23[C@@]1(CC=C2[C@@H](OC(c1c([nH]cc1C)CC)=O)C)OCC[N@@](C3)C)O , |
|
| InChI | InChI : InChI=1/C32H44N2O6/c1-6-23-26(19(2)17-33-23)27(36)39-20(3)22-9-10-31-24-8-7-21-15-30(37)12-11-28(21,4)32(24,40-30)25(35)16-29(22,31)18-34(5)13-14-38-31/h8-9,17,20-21,25,33,35,37H,6-7,10-16,18H2,1-5H3/t20?,21-,25-,28+,29?,30+,31+,32?/m1/s1 |
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| Propriétés chimiques | ||
| Formule | C32H44N2O6 [Isomères] |
|
| Masse molaire[1] | 552,701 6 ± 0,030 9 g/mol C 69,54 %, H 8,02 %, N 5,07 %, O 17,37 %, |
|
| Écotoxicologie | ||
| DL50 | >0,003 mg·kg-1 (souris, i.p.) [2] | |
| Unités du SI et CNTP, sauf indication contraire. | ||
| modifier |
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