유사 구조 검색

308536

CC(C)CCCC(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C
Reaction #173020
DOI: 10.1039/C8SC04228D
CC(C)CCCC(C)C1CCC2C3CC=C4CC(OCCCCCCSC5OC(CO)C(O)C(O)C5O)CCC4(C)C3CCC12C
Reaction #257061
DOI: 10.1039/C8SC04228D
CCCCCCCC/C=C\CCCCCCCC(=O)[O-].[Na+]
Reaction #310878
sodium oleate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #448877
cholesteryl oleate
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 #521325
cholesterol
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)COC(C(=O)N(C)CC[NH+](C)C)(c1ccccc1)c1ccccc1.CCCCC/C=C\C/C=C\CCCCCCCC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]32)C1.[Cl-]
Reaction #528886
X-100 cholesterol linoleate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #669405
cholesteryl oleate
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](OCCCNC(=O)CCC(=O)O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #712322
title compound
수율 114.9%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](OCCCC(=O)O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1140132
4-(Cholest-5-en-3β-yloxy)butanoic acid
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](OCCCC(=O)C(O)CCOCCOCCOCCOCCN)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1140133
[4-(Cholest-5-en-3β-yloxy)butanoyl]-15-amino-4,7,10,13-tetraoxapentadecanol
수율 155.1%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C=C[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](OCCCCCCI)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C
Reaction #1160721
stigmasta-5,22-dien-3β-yl 6-iodohexyl ether
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](OCCCCCCI)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1160722
pregn-5-en-20-one-3β-yl 6-iodohexyl ether
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](OCCCCCCS[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]5O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1160724
product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #1161721
cholesteryl oleate
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](OCCCCCCS[C@@H]5O[C@H](CN)[C@H](O)[C@H](O)[C@H]5O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1193059
6-(5-Cholesten-3β-yloxy)hexyl 6-amino-6-deoxy-1-thio-β-D-galactopyranoside
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@H](OC(C)=O)[C@H](C)O[C@H](SCCCCCCO[C@H]2CC[C@@]3(C)C(=CC[C@H]4[C@@H]5CC[C@H]([C@H](C)CCCC(C)C)[C@@]5(C)CC[C@@H]43)C2)[C@H]1OC(C)=O
Reaction #1193060
title compound
수율 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC1OC(SCCCCCCOC2CCC3(C)C(=CCC4C3CCC3(C)C(C(C)CCCC(C)C)CCC43)C2)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O
Reaction #1219869
DOI: 10.1039/C8SC04228D
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](OCCCCCCS[C@@H]5O[C@H](CN)[C@H](O)[C@H](O)[C@H]5O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1242483
6-(5-Cholesten-3β-yloxy)hexyl 6-amino-6-deoxy-1-thio-β-D-galactopyranoside
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCC(=O)NC[C@H]1O[C@@H](SCCCCCCO[C@H]2CC[C@@]3(C)C(=CC[C@H]4[C@@H]5CC[C@H]([C@H](C)CCCC(C)C)[C@@]5(C)CC[C@@H]43)C2)[C@H](O)[C@@H](O)[C@H]1O
Reaction #1242484
title compound
수율 55.1%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](OCCCCCCCCCC=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1558541
10-(Cholest-5-en-3β-oxy)decanal
DOI: 10.6084/m9.figshare.5104873.v1
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