بحث البنية الفرعية

347248

CC(C)C[C@H](NC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)OC(C)(C)C)C(=O)N[C@@H](C)C(=O)OCc1ccccc1
Reaction #5081
Boc-Leu-Gly-Leu-Ala-OBzl
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)Nc1cnccn1)N1CC(Oc2ccc(C[C@H](O)CO)cc2)=CC1=O
Reaction #47678
(S)-2-{4-[4-((S)-2,3-dihydroxy-propyl)-phenoxy]-2-oxo-2,5-dihydro-pyrrol-1-yl}-4-methyl-pentanoic acid pyrazin-2-ylamide
المردود 68.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)Nc1cnccn1)N1CC(Oc2cccc(CC(C)(C)O)c2)=CC1=O
Reaction #47681
(S)-2-{4-[3-(2-hydroxy-2-methyl-propyl)-phenoxy]-2-oxo-2,5-dihydro-pyrrol-1-yl}-4-methyl-pentanoic acid pyrazin-2-ylamide
المردود 22.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCC(C#N)(NC(=O)C(CC2CCCCC2)N=C(NC(=O)OCC)N2CCOCC2)CC1
Reaction #53520
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCC(C#N)(NC(=O)C(CC2CCCCC2)NC2=NS(=O)(=O)c3ccccc32)CC1
Reaction #53525
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)NC(NC(CC1CCCCC1)C(=O)NC1(C#N)CCN(C)CC1)=S=C=O
Reaction #53535
desired product
المردود 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(NC(=O)C1CC2CCCCC2N1C(=O)C(NC(=O)C(NC(=O)c1cnccn1)C1CCCCC1)C(C)(C)C)C(O)C(=O)OCC
Reaction #70196
32
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H]1C(=O)N[C@H](C2Cc3ccccc3C2)C(=O)N1[C@@H](C(=O)NC(C)C)c1ccc(F)cc1
Reaction #73884
(2R)-2-(4-fluorophenyl)-2-[(3R,6R)-3-(2,3-dihydro-1H-inden-2-yl)-6-isobutyl-2,5-dioxopiperazin-1-yl]-N-isopropylethanamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)C1(NC(=O)OCc2ccccc2)CCCCC1)C(=O)NCC(N)=O
Reaction #93058
1-benzyloxycarbonylaminocyclohex-1-yl-carbonyl-L-leucyl-glycinamide
المردود 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(=O)N[C@H](C(=O)O)C(C)C.C[NH-]
Reaction #93635
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93639
B7
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93642
B7
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(=O)N[C@H](C(=O)N[C@@H](C)C(=O)O)C(C)C.[NH-]CCNCCO
Reaction #93643
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CCCCNC(=O)OC(C)(C)C)C(=O)OC
Reaction #93652
Z-Phe-His-Leu-Val-Ile-His-Lys(BOC)-OMe
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(=O)N[C@H](C(=O)O)C(C)C.[NH-]C(CO)(CO)CO
Reaction #93656
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #95974
methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #95975
methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCCN(CCc1ccccc1)C(=O)NC(CC(C)C)C(=O)N1CCN(C)CC1
Reaction #173878
DOI: 10.1039/C8SC04228D
CNC(=O)C(C)(C)c1ccc(NC(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)cc1
Reaction #187294
DOI: 10.1039/C8SC04228D
CN(CCO)C(=O)CC1CCN(C(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)CC1
Reaction #192114
DOI: 10.1039/C8SC04228D
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