子结构搜索

NCCCCCc1ccc(O)cc1

CCOCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CCCC(Cc1ccc(OC)cc1)S(N)(=O)=O
Reaction #9519
4-methoxybenzyl 4-[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]butane-1-sulfonamide
收率 53.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CCCCS(N)(=O)=O
Reaction #9520
4-[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]butane-1-sulfonamide
收率 77.5%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1CCC(c2ccc(O)cc2)CNC1=O
Reaction #48397
(3R)-3-Amino-6-(4-hydroxyphenyl)azepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2ccc(O)cc2)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48433
title compound
收率 33.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(N)CCCC(C#N)(c2ccc(OC)c(OC)c2)C(C)C)cc1OC
Reaction #93583
1-(3,4-dimethoxyphenyl)-2-amino-6-cyano- 6-(i-propyl)-6-(3,4-dimethoxyphenyl)hexane
收率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C#N)(CCCC2Cc3cc(OC)c(OC)cc3CN2C)C(C)C)cc1OC.Cl
Reaction #93586
3-[4-(3,4-dimethoxyphenyl)-4-isopropyl-4-cyanobutyl]-6,7-dimethoxy-N-methyl-1,2,3,4-tetrahydroisoquinoline·HCl
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)[N-][Si](C)(C)C.[Li+]
Reaction #159240
Lithium bis-(trimethylsilyl)amide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@](O)(CCCC(C)(C)O)C(=O)O[C@@H]1C(OC)=C[C@]23CCCN2CCc2cc4c(cc2[C@H]13)OCO4
Reaction #159241
epi-homoharringtonine
收率 0.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CC(=O)CC(c3ccc(OC)cc3)N2C)cc1
Reaction #164870
white solid
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2(O)CCC3CN(Cc4ccccc4)CCC3C2)cc1
Reaction #173130
DOI: 10.1039/C8SC04228D
CCC(=O)NCCC1CCc2ccc3c(c21)OCO3
Reaction #174997
DOI: 10.1039/C8SC04228D
CC(C)(C)Oc1ccc(CC(NC(=O)OCc2ccccc2)C2OC(C)(C)OC2C(Cc2ccc(OC(C)(C)C)cc2)NC(=O)OCc2ccccc2)cc1
Reaction #179724
DOI: 10.1039/C8SC04228D
CCC(=O)NCCC1CCc2ccc3c(c21)OCO3
Reaction #181080
DOI: 10.1039/C8SC04228D
CC(C(=O)NC(c1ccc(O)cc1)C1CCCN1C(=O)OC(C)(C)C)c1ccccc1
Reaction #183853
DOI: 10.1039/C8SC04228D
COc1ccc2c(c1)CCN1CC3CCCN(S(=O)(=O)CCCN4CCN(c5ccccc5OC)CC4)C3CC21
Reaction #185136
DOI: 10.1039/C8SC04228D
C#CCOc1cc2c(cc1F)CCC2CCNC(=O)CC
Reaction #185483
DOI: 10.1039/C8SC04228D
COc1ccc(CCCC2CN(Cc3ccc(C(C)(C)C)cc3)C(=O)N2C)cc1C
Reaction #195398
DOI: 10.1039/C8SC04228D
COCCCN1CCOc2ccc(COC3CN(S(=O)(=O)c4ccc(C)cc4)C(CC(C)NC(C)=O)CC3c3ccc(OC)cc3)cc21
Reaction #199561
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)Oc1ccc(CCCC(N)C(N)=O)cc1
Reaction #203155
DOI: 10.1039/C8SC04228D
CC(NC(=O)C(NC(=O)C(CCCc1ccc(Oc2ccccc2)c(F)c1)C1OC(C)(C)OC1=O)C(C)(C)C)c1ccccc1
Reaction #203701
DOI: 10.1039/C8SC04228D
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