EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form

Keyword(s):

Human Metabolites

Molecule Category

Free-form


InChI Key	DRBVMPGXZZTVQQ-SHQCIBLASA-N
Smiles	CCCCCCCCCCCCCCCC(=O)OCC(=O)OC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)c1ccc(cc1)[N+]([O-])=O
InChI	InChI=1S/C29H44Cl2N2O8/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-25(34)41-21-26(35)40-20-24(32-29(37)28(30)31)27(36)22-16-18-23(19-17-22)33(38)39/h16-19,24,27-28,36H,2-15,20-21H2,1H3,(H,32,37)/t24-,27-/m1/s1

InChI Key

DRBVMPGXZZTVQQ-SHQCIBLASA-N

Smiles

CCCCCCCCCCCCCCCC(=O)OCC(=O)OC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)c1ccc(cc1)[N+]([O-])=O

InChI

InChI=1S/C29H44Cl2N2O8/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-25(34)41-21-26(35)40-20-24(32-29(37)28(30)31)27(36)22-16-18-23(19-17-22)33(38)39/h16-19,24,27-28,36H,2-15,20-21H2,1H3,(H,32,37)/t24-,27-/m1/s1

Property Name	Value
Molecular Formula	C29H44Cl2N2O8
Molecular Weight	618.25
AlogP	7.32
Hydrogen Bond Acceptor	8.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	23.0
Polar Surface Area	148.56
Heavy Atoms	41.0

Property Name

Value

Molecular Formula

C29H44Cl2N2O8

Molecular Weight

618.25

AlogP

7.32

Hydrogen Bond Acceptor

8.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

23.0

Polar Surface Area

148.56

Heavy Atoms

41.0

Resources	Reference
CAS NUMBER	60595-52-0
NORMAN SUSDAT

Resources

Reference

CAS NUMBER

60595-52-0

NORMAN SUSDAT

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

[R-(R,R)]-2-[2-[(DICHLOROACETYL)AMINO]-3-HYDROXY-3-(4-NITROPHENYL)PROPOXY]-2-OXOETHYL HEXADECANOATE

Structure

Physicochemical Descriptors

Cross References

[R-(R*,R*)]-2-[2-[(DICHLOROACETYL)AMINO]-3-HYDROXY-3-(4-NITROPHENYL)PROPOXY]-2-OXOETHYL HEXADECANOATE

Structure

Physicochemical Descriptors

Cross References

[R-(R,R)]-2-[2-[(DICHLOROACETYL)AMINO]-3-HYDROXY-3-(4-NITROPHENYL)PROPOXY]-2-OXOETHYL HEXADECANOATE