子结构搜索

315302

CCOC(=O)CC(CCCCCCCCCCC(CC(=O)OCC)C(=O)O)NC(=O)OC(C)(C)C
Reaction #5505
diethyl 2-t-butoxycarbonylamino-13-carboxy-1,14-tetradecanedicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(N)CCCCCCCCCCC(CC(=O)OCC)C(=O)O.Cl
Reaction #5506
diethyl 2-amino-13-carboxy-1,14-tetradecanedicarboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1C(=O)C2CC3CC(OC(=O)c4c[nH]c5ccccc45)CC(C2)N31
Reaction #48481
5-(1H-Indole-3-carbonyloxy)-10-oxo-8-aza-tricyclo[5.3.1.03,8]undecane-9-carboxylic acid methyl ester
收率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CC2CC3CC(C1)N2CC3=O)c1c[nH]c2ccccc12
Reaction #48482
1H-Indole-3-carboxylic acid 10-oxo-8-aza-tricyclo[5.3.1.03,8]undec-5-yl ester
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(CCCCCCCCCCC(CC(=O)OCC)C(=O)O)NC(=O)OC(C)(C)C
Reaction #50260
diethyl 2-t-butoxycarbonylamino-13-carboxy-1,14-tetradecanedicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(N)CCCCCCCCCCC(CC(=O)OCC)C(=O)O.Cl
Reaction #50261
diethyl 2-amino-13-carboxy-1,14-tetradecanedicarboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1C[C@@H]2CC[C@@H]3[C@H](CC[C@]4(C)C(=O)[C@@H](N5CCCCC5)C[C@@H]34)[C@@]2(C)C[C@@H]1N1CCCCC1
Reaction #65119
(2β,3α,5α,16β)-3-acetyloxy-2,16-di-(1-piperidinyl)androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](CC(CC1CC2CCC1C2)C(=O)O)C(=O)O.N[C@@H](CC(Cc1ccccc1)C(=O)O)C(=O)O
Reaction #92805
γ-benzyl-L-glutamic acid γ-2-norbornylmethyl-L-glutamic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C12CC3CC(CC(N)(C3)C1C(=O)C(Cc1ccccc1)NC(=O)CNC(=O)C(CCSC)NC(=O)C(Cc1ccc(O)cc1)NC(=O)OC(C)(C)C)C2
Reaction #180583
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCC2C3CCC4CC(OC(C)=O)C(OCC)CC4(C)C3C(NC(=O)OCC(Cl)(Cl)Cl)CC12C
Reaction #181349
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #187241
DOI: 10.1039/C8SC04228D
CN1CCN(C2CC3(C)C(CCC4C3CCC3(C)C(O)C(N5CCCCC5)CC43)CC2O)CC1
Reaction #207559
DOI: 10.1039/C8SC04228D
COC(=O)CCCCCCCCC1(O)OC(COCc2ccccc2)C(OC2OC(CCl)C(Cl)C(OC(C)=O)C2OC(C)=O)C(OC2OC(C)C(OCc3ccccc3)C(OCc3ccccc3)C2OCc2ccccc2)C1NC(C)=O
Reaction #222461
DOI: 10.1039/C8SC04228D
CC(C)C(=O)OC1CC2CCC3C(CCC4(C)C(O)C(N5CCCCC5)CC34)C2(C)CC1N1CCCCC1
Reaction #227637
DOI: 10.1039/C8SC04228D
Cl
Reaction #228032
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #229157
DOI: 10.1039/C8SC04228D
O=C(OC1CC2CC3CC(C1)N2CC3=O)c1c[nH]c2ccccc12
Reaction #241059
DOI: 10.1039/C8SC04228D
CN1C(=O)CCC2(C)C3CCC4(C)C(OCC(=O)O)CCC4C3CCC12
Reaction #262898
DOI: 10.1039/C8SC04228D
CC=C1CCC2C3CCC4CC(O)CCC4(C)C3C(N)CC12C
Reaction #272587
DOI: 10.1039/C8SC04228D
CCOC(=O)COC1CCC2C3CCC4N(C)C(=O)CCC4(C)C3CCC12C
Reaction #272978
DOI: 10.1039/C8SC04228D
第 1 页下一页