بحث البنية الفرعية

C1COCCO1.Cl

CC[C@H](NC(=O)C(CC)(CC)NC(=O)[C@@H](N)CC(=O)O)c1ccccc1
Reaction #867
α-L-aspartyl-α,α-diethylglycine (S)-α-ethylbenzylamide
المردود 29.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](NC(=O)C(C)(CC)NC(=O)[C@@H](N)CC(=O)O)c1ccccc1
Reaction #868
α-L-aspartyl-DL-isovaline (S)-α-ethylbenzylamide
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](N)c1ccccc1.Cl
Reaction #869
(R)-α-methoxymethylbenzylamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC[C@H](N)c1ccccc1.Cl
Reaction #871
(R)-α-ethoxymethylbenzylamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCNC(=O)[C@@H](N)Cc1ccccc1.Cl
Reaction #3880
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCCCNC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@H](N)CCSC.COC(=O)CCCCCNC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@H](N)CCSC.Cl.Cl.O
Reaction #3883
D-methionylglycyl-N-(6-methoxy-6-oxohexyl)-L-phenylalaninamide monohydrochloride hemihydrate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #5432
product
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN2CCCC2C1
Reaction #9983
title compound
المردود 65.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(F)c(F)cc1Nc1ccc(F)cc1F
Reaction #10397
2-(2,4-difluoroanilino)-4,5-difluorobenzoic acid
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)CC(=O)O
Reaction #11101
intermediate 39a
المردود 102.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)[C@H]1CCCN1.Cl
Reaction #11577
(R)-2-pyrrolidinecarboxylic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #11935
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #11939
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #11940
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #11945
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](CCCNCc1ccccn1)C(=O)O)c1ccc(CNc2cccc3cccnc23)cc1
Reaction #11952
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](CCCNc1cccc2cccnc12)C(=O)O)c1ccc(CNCc2ccccn2)cc1
Reaction #11963
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #11964
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
NCC[C@H](NC(=O)c1ccc(CN)cc1)C(=O)O
Reaction #11965
title compound
المردود 189.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #11971
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي