بحث البنية الفرعية

NCC(=O)NCC(N)=O

Cc1cc(O)ccc1C[C@H](N)C(=O)N[C@H](C)C(=O)NCCCc1ccccc1.Cl
Reaction #4861
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1COc2ccc(Cl)cc2CNC(=O)[C@@H]2CCCN2C(=O)[C@@H](C2CCCCC2)NC(=O)CN1
Reaction #6783
(6R,20aS)-16-chloro-6-cyclohexyl-2,3,6,7,9,10,18,19-octahydro-1H-pyrrolo[1,2-j][1,4,7,10,13] benzoxatetraazacyclohexadecine-5,8,11,20 (12H,20aH)-tetrone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](N)C(=O)N[C@H](C(=O)Nc2nc(C(C)=O)cs2)[C@@H](C)c2ccccc2)cc1
Reaction #61086
(2S,3S)-N-(4-acetyl-thiazol-2-yl)-2-[(R)-2-amino-2-(4-methoxy-phenyl)-acetylamino]-3-phenyl-butyramide
المردود 111.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@H]2NC(=O)N([C@H](C(=O)Nc3nc(C(C)=O)cs3)[C@@H](C)c3ccccc3)C2=O)cc1
Reaction #61087
(2S,3S)-N-(4-acetyl-thiazol-2-yl)-2-[(R)-4-(4-methoxy-phenyl)-2,5-dioxo-imidazolidin-1-yl]-3-phenyl-butyramide
المردود 119.8%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1csc(NC(=O)[C@@H](NC(=O)[C@H](N)c2ccc(OCCN3CCCCC3)cc2)[C@@H](C)c2ccccc2)n1
Reaction #61097
(2S,3S)-2-{(R)-2-amino-2-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-acetylamino}-3-phenyl-N-(4-propionyl-thiazol-2-yl)-butyramide
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1csc(NC(=O)[C@H]([C@@H](C)c2ccccc2)N2C(=O)NC(c3ccc(OCCN4CCCCC4)cc3)C2=O)n1
Reaction #61098
(2S,3S)-2-{2,5-dioxo-4-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-imidazolidin-1-yl}-3-phenyl-N-(4-propionyl-thiazol-2-yl)-butyramide
المردود 35.9%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1csc(NC(=O)[C@@H](NC(=O)[C@H](N)c2ccc(OCCN3CCOCC3)cc2)[C@@H](C)c2ccccc2)n1
Reaction #61100
(2S,3S)-2-{(R)-2-amino-2-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-acetylamino}-3-phenyl-N-(4-propionyl-thiazol-2-yl)-butyramide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #61101
solid
المردود 29.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93648
B7
DOI: 10.6084/m9.figshare.5104873.v1
COC1OCCC1NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)c1ccc2c(c1)Nc1ccccc1S2
Reaction #179822
DOI: 10.1039/C8SC04228D
CC(NC(=O)C(CSCC1CCCCC1)NC(=O)C1CSCN1C(=O)NC(C)(C)C)c1ccc([N+](=O)[O-])cc1
Reaction #193634
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCC(=O)NCC(=O)NCC(=O)O
Reaction #202286
DOI: 10.1039/C8SC04228D
CC(C)CC(NC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)OC(C)(C)C)C(=O)NCCC(=O)CCl
Reaction #203288
DOI: 10.1039/C8SC04228D
CN1C(=O)CCC(NC(=O)c2cc(Cl)c(O)c(Cl)c2)C(=O)N1CC(=O)NC(C=O)CC(=O)O
Reaction #203783
DOI: 10.1039/C8SC04228D
CC(C)C[C@H](NC(=O)[C@@H](NC(=O)c1ccccc1)C(C)C)C(=O)O
Reaction #215022
N-benzoyl-L-valyl-L-leucine
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)CC(C)C.O=C(O)C(F)(F)F
Reaction #217175
Leu-DTrp-βAla-OEt.TFA
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)NC(=O)CC(C)(C)C
Reaction #217176
product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCNC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)NC(=O)Nc1ccccc1
Reaction #217177
product
DOI: 10.6084/m9.figshare.5104873.v1
COC1OCC[C@@H]1NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)c1ccc2c(c1)Nc1ccccc1S2
Reaction #218281
yellow solid
المردود 21.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #227361
DOI: 10.1039/C8SC04228D
الصفحة 1التالي