Teilstruktursuche

2670

CC1(C)S[C@@H]2[C@H](NC(=O)CCC[C@H](N)C(=O)O)C(=O)N2[C@H]1C(=O)O
Reaction #1525
isopenicillin N
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)CCC[C@H](N)C(=O)O)C(=O)N2[C@H]1C(=O)O
Reaction #2780
isopenicillin N
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](N)C(=O)N2[C@H]1C(=O)O
Reaction #93272
6-aminopenicillanic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](N)C(=O)N2[C@H]1C(=O)O
Reaction #215179
6-amino-penicillanic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CCC(=O)O)C[C@H](C)C[C@H](C)C(=O)/C=C(\O)[C@H](C)C[C@H](C)C/C=C/[C@@H](C)[C@@H](O)[C@@H](C)[C@@H](O)C[C@@H]1CC[C@@](C)([C@H]2CC[C@@](C)([C@@H](C)O)O2)O1
Reaction #218731
ionomycin
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CCC(=O)O)C[C@H](C)C[C@H](C)C(=O)/C=C(\O)[C@H](C)C[C@H](C)C/C=C/[C@@H](C)[C@@H](O)[C@@H](C)[C@@H](O)C[C@@H]1CC[C@@](C)([C@H]2CC[C@@](C)([C@@H](C)O)O2)O1
Reaction #218820
Ionomycin
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1[C@@H](O)[C@@H](O[C@@H]2[C@@H](O)[C@H](O[C@H]3O[C@H]([C@@H](C)O)[C@@H](O)[C@H](O)[C@H]3N)[C@@H](N)C[C@H]2N)OC[C@]1(C)O
Reaction #304603
G418
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](N)C(=O)N2[C@H]1C(=O)O
Reaction #354364
6-APA
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](N)C(=O)N2[C@H]1C(=O)O
Reaction #354365
6-APS
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(N=C=O)OCc1ccccc1
Reaction #355180
benzyloxy (ethyloxy)phosphinyl isocyanate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #452051
1-ethoxycarbonyloxyethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)CCC[C@H](N)C(=O)O)C(=O)N2[C@H]1C(=O)O
Reaction #463414
isopenicillin N
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)CCC[C@H](N)C(=O)O)C(=O)N2[C@H]1C(=O)O
Reaction #569388
isopenicillin N
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #572866
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(NC(c2ccc([N+](=O)[O-])cc2)c2ccc3cccnc3c2O)n1
Reaction #628209
7-((6-methylpyridin-2-ylamino) (4-nitrophenyl)methyl)quinolin-8-ol
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1[C@@H](O)[C@@H](O[C@@H]2[C@@H](O)[C@H](O[C@H]3O[C@H]([C@@H](C)O)[C@@H](O)[C@H](O)[C@H]3N)[C@@H](N)C[C@H]2N)OC[C@]1(C)O
Reaction #639996
G418
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@H]1CN[C@H](C(=O)O)[C@H]1CC(=O)O
Reaction #659876
Kainate
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O
Reaction #663664
Deoxynojirimycin
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)CCC[C@H](N)C(=O)O)C(=O)N2[C@H]1C(=O)O
Reaction #667961
isopenicillin N
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccn([C@H]2C=C[C@@H](CO)O2)c(=O)n1
Reaction #698655
solutions
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter