Teilstruktursuche

5966

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@](O)(C(=O)OCCl)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1502
3-(Chloromethoxycarbonyl) Cholesterol
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(CC(=O)OCC)C(=O)CCCCCNC(=O)OC1CCC2(C)C(=CCC3C2CCC2(C)C(C(C)CCCC(C)C)CCC32)C1
Reaction #45206
3-({6-[17-(1,5-Dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloxycarbonylamino]-hexanoyl}ethoxycarbonylmethyl-amino)-propionic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(CC(=O)OCC)C(=O)CCCCCNC(=O)OC1CCC2(C)C(=CCC3C2CCC2(C)C(C(C)CCCC(C)C)CCC32)C1
Reaction #49169
3-({6-[17-(1,5-Dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloxycarbonylamino]-hexanoyl}ethoxycarbonylmethyl-amino)-propionic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC(c2ccccc2)C2CN(C(=O)CCCCCNC(=O)OC3CCC4(C)C(=CCC5C4CCC4(C)C(C(C)CCCC(C)C)CCC54)C3)CC2O)c2ccc(OC)cc2)cc1
Reaction #49193
Compound 66
Ausbeute 90.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C.NCCN
Reaction #53249
Cholesterol ethylenediamine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C.CCNC(=N)CCCSSc1ccccn1
Reaction #53250
Cholesterol ethylamidinopropyl-pyridyldisulfide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(CC(=O)OCC)C(=O)CCCCCNC(=O)OC1CCC2(C)C(=CCC3C2CCC2(C)C(C(C)CCCC(C)C)CCC32)C1
Reaction #58787
3-({6-[17-(1,5-Dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloxycarbonylamino]-hexanoyl}ethoxycarbonylmethyl-amino)-propionic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #65344
CHOLESTEROL
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #66034
H+
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #75004
cholesterol
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1O)c1ccc(F)cc1
Reaction #87914
4-Fluoro-N-(2-hydroxyphenyl)-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN(CC(=O)OCC)C(=O)CCCCCNC(=O)OC1CCC2(C)C(=CCC3C2CCC2(C)C(C(C)CCCC(C)C)CCC32)C1
Reaction #89786
3-({6-[17-(1,5-Dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloxycarbonylamino]-hexanoyl}ethoxycarbonylmethyl-amino)-propionic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](N=[N+]=[N-])CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92529
3α-azidocholest-5-ene
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCCC(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C
Reaction #173020
DOI: 10.1039/C8SC04228D
CC(C)CCCC(C)C1CCC2C3C(=O)C=C4CC(O)CCC4(C)C3CCC12C
Reaction #177538
DOI: 10.1039/C8SC04228D
CC(C)CCCC(C)C1CCC2C3CC=C4CC(OC(=O)CCC(=O)O)CCC4(C)C3CCC12C
Reaction #182766
DOI: 10.1039/C8SC04228D
CCOC(C)OC(C)(C)C(F)CCC(COS(=O)(=O)c1ccc(C)cc1)C1CCC2C3CC=C4CC(OC5CCCCO5)CC(OC5CCCCO5)C4(C)C3CCC12C
Reaction #182809
DOI: 10.1039/C8SC04228D
CC(CCCC(C)(O)CO)C1CCC2C3C(Br)C=C4CC(O)CC(O)C4(C)C3CCC12C
Reaction #186987
DOI: 10.1039/C8SC04228D
CC(CCC(O[SiH](C)C)C(C)(C)C)C1CCC2C3C(=O)C=C4CC(OC5CCCCO5)CCC4(C)C3CCC12C
Reaction #198520
DOI: 10.1039/C8SC04228D
CC(=O)O[C@H]1C[C@H](O)CC2=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]3[C@]21C
Reaction #213852
1α-acetoxycholesterol
Ausbeute 107.8%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter