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CCCCCCCCCOC(=O)Cl

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
Выход 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
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
CCCCCCCCCOC(=O)NC(=N)c1ccc(NCc2nc3cc(C(=O)N(CCC(=O)OC)c4ccccn4)ccc3n2C)cc1
Reaction #78593
1-Methyl-2-[N-[4-(N-n-nonyloxycarbonylamidino)phenyl]aminomethyl]benzimidazol-5-yl-carboxylic acid-N-(2-pyridyl)-N-(2-methoxycarbonylethyl)amide
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)OC1C2CC3CC(C2)CC1C3
Reaction #83115
2-Adamantylchloroformate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@](C)(Cc1c[nH]c2ccccc12)NC(=O)OC1C2CC3CC(C2)CC1C3
Reaction #83116
title compound
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[O-]
Reaction #83122
carbonate
Выход 20.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1c[nH]c2ccccc12)N(COC(C)[Si](C)(C)C)C(=O)OC1C2CC3CC(C2)CC1C3
Reaction #83139
title compound
Выход 67.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCOn1nc(N2CCN(CCN3C(=O)c4ccccc4C3=O)CC2)c2ccc(F)cc21.Cl
Reaction #83951
N-[2-[4-(1-decanoxy-6-fluoro-1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide hydrochloride
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
COC(=O)C12CC3CC(C1)C(OC(=O)Cl)C(C3)C2
Reaction #159295
1-(methoxycarbonyl)-4-adamantyl chloroformate
Выход 272.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC1CN(C(=O)OC2C3CC4CC(C3)CC2C4)C1
Reaction #159308
title compound
Выход 23.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCOC(=O)Cl
Reaction #187662
DOI: 10.1039/C8SC04228D
CC(c1c[nH]c2ccccc12)C(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)O
Reaction #229316
DOI: 10.1039/C8SC04228D
Cl
Reaction #252330
DOI: 10.1039/C8SC04228D
CC(=O)OC1C(C)OC(n2cc(F)c(NC(=O)OCCC(C)CCCC(C)CCCC(C)CCCC(C)C)nc2=O)C1OC(C)=O
Reaction #272365
DOI: 10.1039/C8SC04228D
O=C(OCC1CCCCCCCCCC1)n1c(-c2cscn2)nc2ccccc21
Reaction #273607
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCOC(=O)Nc1ccn(C2OC(CO)C(O)C2O)c(=O)n1
Reaction #282590
DOI: 10.1039/C8SC04228D
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