(1'-S,2'-R,3'-S,4'-R,5'-S)-4'-(6-AMINO-2-CHLOROPURIN-9-YL)-2',3'-(DIHYDROXY)-1'-(METHYLPHOSPHONIC_ACID)-BICYCLO-[3.1.0]-HEXANE
Compound with spectra: 1 NMR
![(1'-S,2'-R,3'-S,4'-R,5'-S)-4'-(6-AMINO-2-CHLOROPURIN-9-YL)-2',3'-(DIHYDROXY)-1'-(METHYLPHOSPHONIC_ACID)-BICYCLO-[3.1.0]-HEXANE](/api/compound/EyoXVPrZgYG.png?ph=true&h=300&w=458 "(1'-S,2'-R,3'-S,4'-R,5'-S)-4'-(6-AMINO-2-CHLOROPURIN-9-YL)-2',3'-(DIHYDROXY)-1'-(METHYLPHOSPHONIC_ACID)-BICYCLO-[3.1.0]-HEXANE")
| SpectraBase Compound ID | EyoXVPrZgYG |
|---|---|
| InChI | InChI=1S/C13H17ClN5O4P/c1-24(22,23)3-13-2-5(13)7(8(20)9(13)21)19-4-16-6-10(15)17-12(14)18-11(6)19/h4-5,7-9,20-21H,2-3H2,1H3,(H,22,23)(H2,15,17,18)/t5-,7-,8+,9+,13+/m1/s1 |
| InChIKey | SYZABTSEPKKCPM-XEMBYONJSA-N |
| Mol Weight | 373.74 g/mol |
| Molecular Formula | C13H17ClN5O4P |
| Exact Mass | 373.070669 g/mol |
| Enantiomer InChIKey | SYZABTSEPKKCPM-GPWDXTBVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
[(1R,2R,3S,4R,5S)-4-(6-amino-2-chloropurin-9-yl)-2,3-dihydroxy-1-bicyclo[3.1.0]hexanyl]methoxy-imidazol-1-ylphosphinic acid
(1'-S,2'-R,3'-S,4'-R,5'-S)-4'-(6-AMINO-2-CHLOROPURIN-9-YL)-2',3'-(DIHYDROXY)-1'-[(E)-PHOSPHONOETHENYL]-BICYCLO-[3.1.0]-HEXANE
(1'S,2'R,3'S,4'R,5'S)-4-(6-AMINO-2-METHYLTHIO-9H-PURIN-9-YL)-1-[PHOSPHORYLOXYMETHYL]-BICYCLO-[3.1.0]-HEXANE-2,3-DIOL
(1'S,2'R,3'S,4'R,5'S)-4-(6-AMINO-2-METHYLTHIOOXY-9H-PURIN-9-YL)-1-[PHOSPHORYLOXYMETHYL]-BICYCLO-[3.1.0]-HEXANE-2,3-DIOL
KGUIPQQGSAOMTR-WPLOAARJSA-N
ZSFSXGVOLQGMIJ-BSMQBWNBSA-L
6-N-ACETYL-6-N-ALLYL-2',3',5'-TRIS-O-(tert-BUTYL-DIMETHYLSILYL)-ADENOSINE
6-N-BENZOYL-2',3',5'-TRIS-O-tert-BUTYL-DIMETHYLSILYL-6-N-METHYL-ADENOSINE
1,2,4a,10b-Tetrahydro-4a-methyl-2-(1-methylethyl)benzo[b]naphtho[2,3-d]furan-5,10-dione
1-O-methyl-oureguattidine
| Title | Journal or Book | Year |
|---|---|---|
| Structure−Activity Relationship of (N)-Methanocarba Phosphonate Analogues of 5′-AMP as Cardioprotective Agents Acting Through a Cardiac P2X Receptor | Journal of Medicinal Chemistry | 2010 |