EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	GN7Y8CG66K
EPA CompTox	DTXSID90167333

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

GN7Y8CG66K

EPA CompTox

DTXSID90167333


InChI Key	WMJHGZFQHPCWQZ-GWBBYGMBSA-N
Smiles	CCCCCOC(=O)NC1=NC(=O)N(C=C1F)[C@@H]1O[C@H](C)[C@@H](OC(C)=O)[C@H]1OC(C)=O
InChI	InChI=1S/C19H26FN3O8/c1-5-6-7-8-28-19(27)22-16-13(20)9-23(18(26)21-16)17-15(31-12(4)25)14(10(2)29-17)30-11(3)24/h9-10,14-15,17H,5-8H2,1-4H3,(H,21,22,26,27)/t10-,14-,15-,17-/m1/s1

InChI Key

WMJHGZFQHPCWQZ-GWBBYGMBSA-N

Smiles

CCCCCOC(=O)NC1=NC(=O)N(C=C1F)[C@@H]1O[C@H](C)[C@@H](OC(C)=O)[C@H]1OC(C)=O

InChI

InChI=1S/C19H26FN3O8/c1-5-6-7-8-28-19(27)22-16-13(20)9-23(18(26)21-16)17-15(31-12(4)25)14(10(2)29-17)30-11(3)24/h9-10,14-15,17H,5-8H2,1-4H3,(H,21,22,26,27)/t10-,14-,15-,17-/m1/s1

Property Name	Value
Molecular Formula	C19H26F1N3O8
Molecular Weight	443.17
AlogP	1.92
Hydrogen Bond Acceptor	10.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	8.0
Polar Surface Area	138.54
Heavy Atoms	31.0

Property Name

Value

Molecular Formula

C19H26F1N3O8

Molecular Weight

443.17

AlogP

1.92

Hydrogen Bond Acceptor

10.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

8.0

Polar Surface Area

138.54

Heavy Atoms

31.0

Resources	Reference
CAS NUMBER	162204-20-8
NORMAN SUSDAT
FDA SRS	GN7Y8CG66K
PubChem	73425552
ChemSpider	22378824.0

Resources

Reference

CAS NUMBER

162204-20-8

NORMAN SUSDAT

FDA SRS

GN7Y8CG66K

PubChem

73425552

ChemSpider

22378824.0

EcoDrug+ was developed under the PREMIER Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information EcoDrug+ contains.

Elements of EcoDrug+ were developed under the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT Center for Science Ltd is thanked for providing computational resources. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

Content of EcoDrug+ is provided without guarantee for correctness.

Cite Us:

Ashenafi Legehar, Siobhán Monaghan, Mael Briand, Akseli Niemelä, Leo Ghemtio, Ziaurrehman Tanoli, A Ross Brown, Charles R Tyler, Henri Xhaard, EcoDrug PLUS: an advanced database for drug target conservation analysis and environmental risk assessment, Nucleic Acids Research, 2025, gkaf1251 Read...

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

2',3'-DI-O-ACETYL-5'-DEOXY-5-FLUORO-N4-(PENTYLOXYCARBONYL)CYTIDINE

Structure

Physicochemical Descriptors

Cross References