C39H46FN4O8P Uridine, 5′ -O- [bis(4-methoxyphenyl)phenylmethyl]-2′ -deoxy-2′ – fluoro-, 3′ – [2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite] (ACI)

productio

C39H46FN4O8P Uridine, 5′ -O- [bis(4-methoxyphenyl)phenylmethyl]-2′ -deoxy-2′ – fluoro-, 3′ – [2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite] (ACI)

Basic Information:


Product Detail

Product Tags

Substantia detail

Cas Subcriptio Number

146954-75-8

Key physica proprietatibus Valor Conditio
Pondus 748,78 -
Pka (praedicta) 9.39 ± 0.10 Most Acidic Temp: XXV ° C

Alia nomina et identifiers

Canonica ridet

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 = c5 = C5

INCHI

Inchi = 1s / c39h46fn4o8p / c1-26 (II) XLIV (XXVII (III) IV) LIII (50-24-10-22-41) 52-36-33 (51-37 (XXXV) 42-38 (XLIII) XLVI) -8-7-9-12-28,29-13-17-31 (47-5) 18-14-29) 30-15-19-32 (48-6) 20-16-30 / H7-9,11-21,23,26-27,335-37h, 10,24-25H2,1-6H3 (H, 42,45,46) / T3 3 35-, 36-, 37-, LIII? / M1 / ​​S1

Key Inchi

HQHQPayRJJMYQX, Djtpzymwsa, N

I aliud nomen huius substantiae

Uridine, V '-O- [bis (IV-metoxyphen) Phenylmethyl] -2, -Doxy-II '-fluoro-, III' - [II-cyanoethyl- bis (I-methylethyl) phosphoramidite] (9CI)

Proprietatibus praesto
Biological
Proiectus
Lipinski
Structuram related

Biological

Res Valor Conditio Fons
Bioconcentration factor CDLVII PH I; Temp: XXV ° C (I) ACD
Bioconcentration factor MMMDCXC PH II; Temp: XXV ° C (I) ACD
Bioconcentration factor (XXVII) DCC PH III; Temp: XXV ° C (I) ACD
Bioconcentration factor (LXXXII) CM PH IV; Temp: XXV ° C (I) ACD
Bioconcentration factor 1.04 x CV PH V; Temp: XXV ° C (I) ACD
Bioconcentration factor 1.06 x CV Ph VI; Temp: XXV ° C (I) ACD
Bioconcentration factor 1.06 x CV PH VII; Temp: XXV ° C (I) ACD
Bioconcentration factor 1.02 x CV PH VIII; Temp: XXV ° C (I) ACD
Bioconcentration factor (LXXVI) CC PH IX; Temp: XXV ° C (I) ACD
Bioconcentration factor (XXII) PH X; Temp: XXV ° C (I) ACD

(I) Calculus in ratione progressionem progressionem (ACD / Labs) Software V11.02 (© 1994-2023 ACD / Labs)

Proiectus

Property valorem condicionem fontem
Koc DXCII PH I; Temp: XXV ° C (I) ACD
Koc (IV) DCCXC PH II; Temp: XXV ° C (I) ACD
Koc (XXXVI) PH III; Temp: XXV ° C (I) ACD
Koc 1.07 x CV PH IV; Temp: XXV ° C (I) ACD
Koc 1.34 X CV PH V; Temp: XXV ° C (I) ACD
Koc 1.38 X CV PH VI; Temp: XXV ° C (I) ACD
Koc 1.37 X CV PH VII; Temp: XXV ° C (I) ACD
Koc 1.33 X CV PH VIII; Temp: XXV ° C (I) ACD
Koc (XCVIII) DCCC PH IX; Temp: XXV ° C (I) ACD
Koc (XXVIII) DC pH X; Temp: XXV ° C (I) ACD
Logd 4.55 PH I; Temp: XXV ° C (I) ACD
Langel 5.46 pH II; Temp: XXV ° C (I) ACD
Langel 5.33 pH III; Temp: XXV ° C (I) ACD

 

Res Valor Conditio Fons
logd 6.81 PH IV; Temp: XXV ° C (I) ACD
logd 6,91 PH V; Temp: XXV ° C (I) ACD
logd 6.92 Ph VI; Temp: XXV ° C (I) ACD
logd 6.92 PH VII; Temp: XXV ° C (I) ACD
logd 6,90 PH VIII; Temp: XXV ° C (I) ACD
logd 6,77 PH IX; Temp: XXV ° C (I) ACD
logd 6,23 PH X; Temp: XXV ° C (I) ACD
logp 6,918 ± 0.641 Temp: XXV ° C (I) ACD
Missam intrinsecam solubility 2.2 x 10-5 g / l Temp: XXV ° C (I) ACD
Missam solubility 5.1 X 10-3 g / l PH I; Temp: XXV ° C (I) ACD
Missam solubility 6.3 x 10-4 g / l PH II; Temp: XXV ° C (I) ACD
Missam solubility 8.2 x 10-5 g / l PH III; Temp: XXV ° C (I) ACD
Missam solubility 2.8 x 10-5 g / l PH IV; Temp: XXV ° C (I) ACD
Missam solubility 2.2 x 10-5 g / l PH V; Temp: XXV ° C (I) ACD
Missam solubility 2.2 x 10-5 g / l Ph VI; Temp: XXV ° C (I) ACD
Missam solubility 2.2 x 10-5 g / l PH VII; Temp: XXV ° C (I) ACD
Missam solubility 2.2 x 10-5 g / l PH VIII; Temp: XXV ° C (I) ACD
Missam solubility X 10-5 g / l PH IX; Temp: XXV ° C (I) ACD
Missam solubility X 10-4 G / l PH X; Temp: XXV ° C (I) ACD
Missam solubility 2.2 x 10-5 g / l Unbuffered aqua PH 7.00; Temp: XXV ° C (I) ACD
Molaris intrinsecam solubility 2.9 x 10-8 Mol / l Temp: XXV ° C (I) ACD
Molaris solubility 6,8 x 10-6 Mol / l PH I; Temp: XXV ° C (I) ACD
Molaris solubility 8.4 x 10-7 Mol / l PH II; Temp: XXV ° C (I) ACD
Molaris solubility X 10-7 Mol X / l PH III; Temp: XXV ° C (I) ACD
Molaris solubility 10-8 Mol X 3.7 / l PH IV; Temp: XXV ° C (I) ACD
Molaris solubility 10-8 Mol X 3.0 / l PH V; Temp: XXV ° C (I) ACD
Molaris solubility 2.9 x 10-8 Mol / l Ph VI; Temp: XXV ° C (I) ACD
Molaris solubility 2.9 x 10-8 Mol / l PH VII; Temp: XXV ° C (I) ACD
Molaris solubility 10-8 Mol X 3.0 / l PH VIII; Temp: XXV ° C (I) ACD
Molaris solubility 4.0 X 10-8 Mol / l PH IX; Temp: XXV ° C (I) ACD
Molaris solubility X 10-7 Mol / l PH X; Temp: XXV ° C (I) ACD
Molaris solubility 2.9 x 10-8 Mol / l Unbuffered aqua PH 7.00; Temp: XXV ° C (I) ACD

 

Res Valor Conditio Fons
Pondus 748,78    
PKA 9.39 ± 0.10 Most Acidic Temp: XXV ° C (I) ACD
PKA 3.45 ± 0.70 Maxime basic temp: XXV ° (I) ACD

(I) Calculus in ratione progressionem progressionem (ACD / Labs) Software V11.02 (© 1994-2023 ACD / Labs)

Lipinski

Res Valor Conditio Fons
Sponte Rotatable vincula 17   (I) ACD
H acceptors 12   (I) ACD
H donos 1   (I) ACD
H donator / Acceptor Sum 13   (I) ACD
logp 6,918 ± 0.641 Temp: XXV ° C (I) ACD
Pondus 748,78    

(I) Calculus in ratione progressionem progressionem (ACD / Labs) Software V11.02 (© 1994-2023 ACD / Labs)

Structuram related

Res Valor Source
Polar superficies regio CXLV A2 (I) ACD

(I) Calculus in ratione progressionem progressionem (ACD / Labs) Software V11.02 (© 1994-2023 ACD / Labs)


  • Previous:
  • Next:

  • Scribere nuntium hic mitte nobis