Glu

NC(N)=O.N[C@@H](CCC(=O)O)C(=O)O.c1c[nH]cn1
Reaction #84603
Glu urea imidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C1CC[C@@H](C(=O)O)O1
Reaction #89014
crude product
المردود 63.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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.v1uspto-grants-2016_09
NC(N)=O.N[C@@H](CCC(=O)O)C(=O)O.c1c[nH]cn1
Reaction #164796
Glu urea imidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cl.N[C@@H](CCC(=O)O)C(=O)O
Reaction #318645
glutamic acid monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CCCCCCCCC=CCCCCCCCC(=O)OC(CCCCCCCC=CCCCCCCCC)CC(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)O)C(C)C
Reaction #323672
N-[N-[3-(9-octadecenoyloxy)-11-eicosenoyl]-L-valyl]-L-glutamic acid
المردود 31.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CCCCCCCCCCCCCCCC(=O)OC(CCCCCCCCCCCCCCC)CC(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)N[C@@H](CCC(=O)O)C(=O)O
Reaction #323679
N-[Nα -(3-hexadecanoyloxyoctadecanoyl)-Nε -benzyloxycarbonyl-L-lysyl]-L-glutamic acid
المردود 68.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #342763
L-glutamyl-L-phenylalanine benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
CC(=O)OCC[C@H](N)C(=O)O
Reaction #342792
γ-methyl L-glutamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
—
Reaction #364796
cyclic amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
N[C@@H](CCC(=O)O)C(=O)O.Nc1nc(C[C@H](N)C(=O)O)cs1
Reaction #413588
3-(2-amino-4-thiazolyl)-L-alanine L-glutamic acid salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
C=CCOC(=O)CCC(N)C(=O)O
Reaction #429290
2-amino-pentanedioic acid 5-allyl ester
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
N[C@@H](CS)C(=O)O
Reaction #430453
Cys
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
NCCCC[C@H](N)C(=O)O
Reaction #431818
Lys
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
N[C@@H](CC(=O)O)C(=O)O.N[C@@H](CCC(=O)O)C(=O)O.N[C@@H](Cc1ccc(O)cc1)C(=O)O.N[C@@H](Cc1ccccc1)C(=O)O
Reaction #443973
Glu Asp Tyr Phe
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
O=C(O)CC[C@@H](C(=O)O)N1C(=O)c2ccccc2C1=O
Reaction #451397
N,N-phthaloylglutamic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
CC(C)C[C@H](N)C(=O)O
Reaction #456197
Leu
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CC(C)C[C@H](N)C(=O)O
Reaction #456199
Leu
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CC(C)C[C@H](N)C(=O)O
Reaction #456200
Leu
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CC(O)[C@H](C)[C@H](N)C(=O)O
Reaction #470402
4-hydroxyisoleucine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
الصفحة 1التالي