![C39H46FN4O8P Uridine, 5′ -O- [bis(4-methoxyphenyl)phenylmethyl]-2′ -deoxy-2′ - fluoro-, 3′ - [2-cyanoethyl N, N-bis(1-methylethyl) phosphoramidite] (ACI. )](http://cdn.globalso.com/nvchem/style/global/img/demo/page_banner.jpg)
![C39H46FN4O8P Uridine, 5′ -O- [bis(4-methoxyphenyl)phenylmethyl]-2′ -deoxy-2′ - fluoro-, 3′ - [2-cyanoethyl N, N-bis(1-methylethyl) phosphoramidite] (ACI. ) Image Featured](https://cdn.globalso.com/nvchem/C39H46FN4O8P-Uridine.png)
C39H46FN4O8P Uridine, 5′ -O- [bis(4-methoxyphenyl)phenylmethyl]-2′ -deoxy-2′ - fluoro-, 3′ - [2-cyanoethyl N, N-bis(1-methylethyl) phosphoramidite] (ACI. )
CAS Subcriptio Number
146954-75-8
| Key Physical Properties | Precium | Conditio |
| M. Pondus | 748.78 | - |
| pKa (Predicta) | 9.39±0.10 | Most acidic Temp: 25 °C |
CANONICI SMILES
N#CCCOP(OC1C(F)C(OC1COC(C=2C=CC=CC2)(C3=CC=C(OC)C=C3)C4=CC=C(OC)C=C4)N5C=CC(= O)NC5=O)N(C(C)C)C(C)C
Isomeric SMILES
C(OC[C@@H]1[C@@H](OP(N(C(C)C)C(C)C)OCCC#N)[C@@H](F)[C@@ H](O1)N2C(=O)NC(=O)C=C2)(C3=CC=C(OC)C=C3)(C4=CC=C(OC)C=C4)C5=CC=CC =C5
InChI'
InChI= 1S/C39H46FN4O8P/c1-26(2)44(27(3)4)53(50-24-10-22-41)52-36-33(51-37(35(36)40)43- 23-21-34(45)42-38(43)46)25-49-39(28-11 -8-7-9-12-28,29-13-17-31(47-5)18- 14-29)30-15-19-32(48-6)20-16-30/h7-9,11-21,23,26-27,33,35-37H,10,24-25H2,1- 6H3,(H,42,45,46)/t3 3-,35-,36-,37-,53?/m1/s1
InChI Key
HQHQPAYRJJMYQX-DJTPZYMWSA-N
1 Alii nomen huic substantiae
Uridine, 5′ -O- [bis(4-methoxyphenyl)phenylmethyl]-2′ -deoxy-2′ -fluoro-, 3′ - [2-cyanoethyl bis(1-methylethyl)phosphoramidite] (9CI)
Properties praesto
Biological
Chemical
Lipinski
Structure Related
| Property | Precium | Conditio | Source |
| Bioconcentration Factor | 457 | pH 1; Temp: 25 °C | (1) ACD |
| Bioconcentration Factor | 3690 | pH 2; Temp: 25 °C | (1) ACD |
| Bioconcentration Factor | 27700 | pH 3; Temp: 25 °C | (1) ACD |
| Bioconcentration Factor | 82900 | pH 4; Temp: 25 °C | (1) ACD |
| Bioconcentration Factor | 1.04 x 105 | pH 5; Temp: 25 °C | (1) ACD |
| Bioconcentration Factor | 1.06 x 105 | pH 6; Temp: 25 °C | (1) ACD |
| Bioconcentration Factor | 1.06 x 105 | pH 7; Temp: 25 °C | (1) ACD |
| Bioconcentration Factor | 1.02 x 105 | pH 8; Temp: 25 °C | (1) ACD |
| Bioconcentration Factor | 76200 | pH 9; Temp: 25 °C | (1) ACD |
| Bioconcentration Factor | 22000 | pH 10; Temp: 25 °C | (1) ACD |
(1) Calculata per Progressionem Chemiae Provectus (ACD/Labs) Software V11.02 (© 1994-2023 ACD/Labs)
| Res eae conditione Source |
| Koc 592 pH 1; Temp: 25 °C (1) ACD |
| Koc 4790 pH 2; Temp: 25 °C (1) ACD |
| Koc 36000 pH 3; Temp: 25 °C (1) ACD |
| Koc 1.07 x 105 pH 4; Temp: 25 °C (1) ACD |
| Koc 1.34 x 105 pH 5; Temp: 25 °C (1) ACD |
| Koc 1.38 x 105 pH 6; Temp: 25 °C (1) ACD |
| Koc 1.37 x 105 pH 7; Temp: 25 °C (1) ACD |
| Koc 1.33 x 105 pH 8; Temp: 25 °C (1) ACD |
| Koc 98800 pH 9; Temp: 25 °C (1) ACD |
| Koc 28600 pH 10; Temp: 25 °C (1) ACD |
| logD 4.55 pH 1; Temp: 25 °C (1) ACD |
| logD 5.46 pH 2; Temp: 25 °C (1) ACD |
| logD 6.33 pH 3; Temp: 25 °C (1) ACD |
| Property | Precium | Conditio | Source |
| logD | 6.81 | pH 4; Temp: 25 °C | (1) ACD |
| logD | 6.91 | pH 5; Temp: 25 °C | (1) ACD |
| logD | 6.92 | pH 6; Temp: 25 °C | (1) ACD |
| logD | 6.92 | pH 7; Temp: 25 °C | (1) ACD |
| logD | 6.90 | pH 8; Temp: 25 °C | (1) ACD |
| logD | 6.77 | pH 9; Temp: 25 °C | (1) ACD |
| logD | 6.23 | pH 10; Temp: 25 °C | (1) ACD |
| logP | 6.918±0.641 | Temp: 25 °C | (1) ACD |
| Missa Solubilitas intrinseca | 2.2 x 10-5 g/L | Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 5.1 x 10-3 g/L | pH 1; Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 6.3 x 10-4 g/L | pH 2; Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 8.2 x 10-5 g/L | pH 3; Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 2.8 x 10-5 g/L | pH 4; Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 2.2 x 10-5 g/L | pH 5; Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 2.2 x 10-5 g/L | pH 6; Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 2.2 x 10-5 g/L | pH 7; Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 2.2 x 10-5 g/L | pH 8; Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 3.0 x 10-5 g/L | pH 9; Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 1.0 x 10-4 g/L | pH 10; Temp: 25 °C | (1) ACD |
| Missa Solubilitas | 2.2 x 10-5 g/L | Aquam gratuitam pH 7.00; Temp: 25 °C | (1) ACD |
| Molares Intrinsicas Solubility | 2.9 x 10-8 mol/L | Temp: 25 °C | (1) ACD |
| Molares Solubility | 6.8 x 10-6 mol/L | pH 1; Temp: 25 °C | (1) ACD |
| Molares Solubility | 8.4 x 10-7 mol/L | pH 2; Temp: 25 °C | (1) ACD |
| Molares Solubility | 1.1 x 10-7 mol/L | pH 3; Temp: 25 °C | (1) ACD |
| Molares Solubility | 3.7 x 10-8 mol/L | pH 4; Temp: 25 °C | (1) ACD |
| Molares Solubility | 3.0 x 10-8 mol/L | pH 5; Temp: 25 °C | (1) ACD |
| Molares Solubility | 2.9 x 10-8 mol/L | pH 6; Temp: 25 °C | (1) ACD |
| Molares Solubility | 2.9 x 10-8 mol/L | pH 7; Temp: 25 °C | (1) ACD |
| Molares Solubility | 3.0 x 10-8 mol/L | pH 8; Temp: 25 °C | (1) ACD |
| Molares Solubility | 4.0 x 10-8 mol/L | pH 9; Temp: 25 °C | (1) ACD |
| Molares Solubility | 1.4 x 10-7 mol/L | pH 10; Temp: 25 °C | (1) ACD |
| Molares Solubility | 2.9 x 10-8 mol/L | Aquam gratuitam pH 7.00; Temp: 25 °C | (1) ACD |
| Property | Precium | Conditio | Source |
| M. Pondus | 748.78 | ||
| pKa | 9.39±0.10 | Most acidic Temp: 25 °C | (1) ACD |
| pKa | 3.45±0.70 | Most Basic Temp: 25 °C | (1) ACD |
(1) Calculata per Progressionem Chemiae Provectus (ACD/Labs) Software V11.02 (© 1994-2023 ACD/Labs)
| Property | Precium | Conditio | Source |
| Sponte rotatable vincula | 17 | (1) ACD | |
| H. Acceptores | 12 | (1) ACD | |
| H Donors | 1 | (1) ACD | |
| H Donor/Acceptor Sum | 13 | (1) ACD | |
| logP | 6.918±0.641 | Temp: 25 °C | (1) ACD |
| M. Pondus | 748.78 |
(1) Calculata per Progressionem Chemiae Provectus (ACD/Labs) Software V11.02 (© 1994-2023 ACD/Labs)
| Property | Precium | Conditio Source |
| Superficies Polar Area | 145 A2 | (1) ACD |
(1) Calculata per Progressionem Chemiae Provectus (ACD/Labs) Software V11.02 (© 1994-2023 ACD/Labs)
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