C11h15n5o5 Guanosine, II, -o-methyl- (7ci, 8ci, 9CI, ACI)
Cas Subcriptio Number
2140-71-8
| Key physica proprietatibus | Valor | Conditio |
| Pondus | 297,27 | - |
| Melting Point (experimentalem) | 233-235 ° C | Solvente: Methanol |
| Density (praedicta) | 1.98 ± 0.1 G / CM3 | Temp: XX ° C; Press: DCCLX Torr |
| Pka (praedicta) | 9.64 ± 0.20 | Most Acidic Temp: XXV ° C |
Canonica ridet
O = C1n = C (n) NC2 = C1N = CN2C3OC (Co) C (o) C3OC
Isomeric smiles
O (c) [C @ h] I [C @ h] (n2c3 = c (n = C2) C (= o) n = c (n3) [c @] (co) [c @] (C) [c @] (C) [C @] 1o
INCHI
Inchi = 1s / c11h15n5o5 / C1-20-7-6 (XVIII) IV (2-17) 21-10 (VII) 16-3-13-5-8 (XVI), 14-11 (XII) 15-9 (V) XIX / H3-4,6-7,17-18 / T4-, 6, 7-, 10- / M1 / S1
Key Inchi
Ovyngsfvyrprcg, kqynxxxcusa, n
I aliud nomen huius substantiae
II '-O-Methylguanosine (aci)
Proprietatibus praesto
Proiectus
Scelerum
| Res | Valorem condicionem | Fons |
| PKA | 9,5 | (I) CAS |
(I) Bhamra, indur; Nucleic acidis investigationis,
| Res | Valor | Conditio | Fons |
| Point liquescens | 233-235 ° C | Solvente: Methanol | (I) CAS |
(I) Core, Anilkumar R.; Nucleosides, nucleic acida & nucleeotides;
Spectra praesto
I h NMR
XIII c NMR
Missa
Proprietatibus praesto
Biological
Proiectus
Densitas
Lipinski
Structuram related
| Res | Valor | Conditio | Fons |
| Bioconcentration factor | 1.0 | PH I; Temp: XXV ° C | (I) ACD |
| Bioconcentration factor | 1.0 | PH II; Temp: XXV ° C | (I) ACD |
| Bioconcentration factor | 1.0 | PH III; Temp: XXV ° C | (I) ACD |
| Bioconcentration factor | 1.0 | PH IV; Temp: XXV ° C | (I) ACD |
| Bioconcentration factor | 1.0 | PH V; Temp: XXV ° C | (I) ACD |
| Bioconcentration factor | 1.0 | Ph VI; Temp: XXV ° C | (I) ACD |
| Res | Valor | Conditio | Fons |
| Bioconcentration factor | 1.0 | PH VII; Temp: XXV ° C | (I) ACD |
| Bioconcentration factor | 1.0 | PH VIII; Temp: XXV ° C | (I) ACD |
| Bioconcentration factor | 1.0 | PH IX; Temp: XXV ° C | (I) ACD |
| Bioconcentration factor | 1.0 | PH X; Temp: XXV ° C | (I) ACD |
(I) Calculus in ratione progressionem progressionem (ACD / Labs) Software V11.02 (© 1994-2023 ACD / Labs)
| Res | Valor | Conditio | Fons |
| Koc | 1.0 | PH I; Temp: XXV ° C | (I) ACD |
| Koc | 1,19 | PH II; Temp: XXV ° C | (I) ACD |
| Koc | 3.42 | PH III; Temp: XXV ° C | (I) ACD |
| Koc | 4.23 | PH IV; Temp: XXV ° C | (I) ACD |
| Koc | 4.33 | PH V; Temp: XXV ° C | (I) ACD |
| Koc | 4.34 | Ph VI; Temp: XXV ° C | (I) ACD |
| Koc | 4.33 | PH VII; Temp: XXV ° C | (I) ACD |
| Koc | 4.24 | PH VIII; Temp: XXV ° C | (I) ACD |
| Koc | 3.48 | PH IX; Temp: XXV ° C | (I) ACD |
| Koc | 1.28 | PH X; Temp: XXV ° C | (I) ACD |
| logd | -2.76 | PH I; Temp: XXV ° C | (I) ACD |
| logd | -1.92 | PH II; Temp: XXV ° C | (I) ACD |
| logd | -1.46 | PH III; Temp: XXV ° C | (I) ACD |
| logd | -1.37 | PH IV; Temp: XXV ° C | (I) ACD |
| logd | -1.36 | PH V; Temp: XXV ° C | (I) ACD |
| logd | -1.36 | Ph VI; Temp: XXV ° C | (I) ACD |
| logd | -1.36 | PH VII; Temp: XXV ° C | (I) ACD |
| logd | -1.37 | PH VIII; Temp: XXV ° C | (I) ACD |
| logd | -1.45 | PH IX; Temp: XXV ° C | (I) ACD |
| logd | -1.89 | PH X; Temp: XXV ° C | (I) ACD |
| logp | -1,359 ± 0.544 | Temp: XXV ° C | (I) ACD |
| Missam intrinsecam solubility | 1.1 g / l | Temp: XXV ° C | (I) ACD |
| Missam solubility | XXVII g / l | PH I; Temp: XXV ° C | (I) ACD |
| Missam solubility | 3,9 g / l | PH II; Temp: XXV ° C | (I) ACD |
| Missam solubility | 1.4 g / l | PH III; Temp: XXV ° C | (I) ACD |
| Missam solubility | 1.1 g / l | PH IV; Temp: XXV ° C | (I) ACD |
| Res | Valor | Conditio | Fons |
| Missam solubility | 1.1 g / l | PH V; Temp: XXV ° C | (I) ACD |
| Missam solubility | 1.1 g / l | Ph VI; Temp: XXV ° C | (I) ACD |
| Missam solubility | 1.1 g / l | PH VII; Temp: XXV ° C | (I) ACD |
| Missam solubility | 1.1 g / l | PH VIII; Temp: XXV ° C | (I) ACD |
| Missam solubility | 1.3 g / l | PH IX; Temp: XXV ° C | (I) ACD |
| Missam solubility | 3,6 g / l | PH X; Temp: XXV ° C | (I) ACD |
| Missam solubility | 1.1 g / l | Unbuffered aqua 6,17; Temp: XXV ° C | (I) ACD |
| Molaris intrinsecam solubility | 3,6 x 10-3 mol / l | Temp: XXV ° C | (I) ACD |
| Molaris solubility | 0.091 MOL / l | PH I; Temp: XXV ° C | (I) ACD |
| Molaris solubility | 0.013 MOL / l | PH II; Temp: XXV ° C | (I) ACD |
| Molaris solubility | X 10-3 Mol / l | PH III; Temp: XXV ° C | (I) ACD |
| Molaris solubility | 10-3 Mol 3.7 / l | PH IV; Temp: XXV ° C | (I) ACD |
| Molaris solubility | 10-3 Mol 3.7 / l | PH V; Temp: XXV ° C | (I) ACD |
| Molaris solubility | 3,6 x 10-3 mol / l | Ph VI; Temp: XXV ° C | (I) ACD |
| Molaris solubility | 10-3 Mol 3.7 / l | PH VII; Temp: XXV ° C | (I) ACD |
| Molaris solubility | 10-3 Mol 3.7 / l | PH VIII; Temp: XXV ° C | (I) ACD |
| Molaris solubility | X 10-3 Mol / l | PH IX; Temp: XXV ° C | (I) ACD |
| Molaris solubility | 0.012 MOL / l | PH X; Temp: XXV ° C | (I) ACD |
| Molaris solubility | 3,6 x 10-3 mol / l | Unbuffered aqua 6,17; Temp: XXV ° C | (I) ACD |
| Pondus | 297,27 | ||
| PKA | 9.64 ± 0.20 | Most Acidic Temp: XXV ° C | (I) ACD |
| PKA | 2.42 ± 0.10 | Maxime basic temp: XXV ° | (I) ACD |
(I) Calculus in ratione progressionem progressionem (ACD / Labs) Software V11.02 (© 1994-2023 ACD / Labs)
| Res | Valor | Conditio | Fons |
| Densitas | 1.98 ± 0.1 G / CM3 | Temp: XX ° C; Press: DCCLX Torr | (I) ACD |
| Molaris volumine | 149.8 ± 7.0 CM3 / mol | Temp: XX ° C; Press: DCCLX Torr | (I) ACD |
(I) Calculus in ratione progressionem progressionem (ACD / Labs) Software V11.02 (© 1994-2023 ACD / Labs)
| Res | Valor | Source |
| Sponte Rotatable vincula | 5 | (I) ACD |
| Res | Valor | Conditio | Fons |
| H acceptors | 10 | (I) ACD | |
| H donos | 5 | (I) ACD | |
| H donator / Acceptor Sum | 15 | (I) ACD | |
| logp | -1,359 ± 0.544 | Temp: XXV ° C | (I) ACD |
| Pondus | 297,27 |
(I) Calculus in ratione progressionem progressionem (ACD / Labs) Software V11.02 (© 1994-2023 ACD / Labs)
| Res | Valor | Source |
| Polar superficies regio | CXLIV A2 | (I) ACD |
(I) Calculus in ratione progressionem progressionem (ACD / Labs) Software V11.02 (© 1994-2023 ACD / Labs)
Spectra praesto
I h NMR
XIII c NMR
![C21H21N3O6 Thymidine, α - [(I-Naphthalenylenylenyl) amino] - α -Oxo- (ACI)](https://cdn.globalso.com/nvchem/C21H21N3O6-Thymidine-300x300.png)
![C10H12N2O5 6H-Furo[2′,3′:4,5]oxazolo[3,2-a]pyrimidin-6-one, 2,3,3a,9a-tetrah ydro-3-hydroxy-2-(hydroxymethyl)-7-methyl-, (2R,3 R,3aS,9aR)- (9CI, ACI)](https://cdn.globalso.com/nvchem/C10H12N2O5-6H-Furo-300x300.jpg)
![C9h10n2o5 6h-Furo [II ', III, 4,5] Oxazolo [3,2-a] Pyrimidin-VI-unum, 2,3,3a, 2, 9a-TETRA-VI-Hydroxy-2- (Hydroxymethyl, III-Hydroxy-2R, 9a-TETRA-VI-Hydroxy-2R (Hydroxymethyl), Hydroxy-2R, 9a-TETRHA ydro-III-hydroxy-2r, 9a-TETRH-III-Hydroxy-2r, 9a-TETRH) - (2r, III R, 3as, 9ar) - (9c, 3as, 9ar) - (9c, 3s), 9AR) - (9c, 3as) - (9c, 3s), 9ar) - (9c, 3as)](https://cdn.globalso.com/nvchem/C9H10N2O5-6H-Furo-300x300.png)