EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Salt-form
EPA CompTox	DTXSID90887281

Keyword(s):

Human Metabolites

Molecule Category

Salt-form

EPA CompTox

DTXSID90887281


InChI Key	VFFMBHXEAASUMC-UHFFFAOYSA-N
Smiles	O=C(O)C.O=C(N)CCN(CCNC(=O)CCCCCCCCCCCCCCCCC)CCN(CCC(=O)N)CCC(=O)N
InChI	InChI=1/C31H62N6O4.C2H4O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-31(41)35-21-25-37(24-20-30(34)40)27-26-36(22-18-28(32)38)23-19-29(33)39;1-2(3)4/h2-27H2,1H3,(H2,32,38)(H2,33,39)(H2,34,40)(H,35,41);1H3,(H,3,4)

InChI Key

VFFMBHXEAASUMC-UHFFFAOYSA-N

Smiles

O=C(O)C.O=C(N)CCN(CCNC(=O)CCCCCCCCCCCCCCCCC)CCN(CCC(=O)N)CCC(=O)N

InChI

InChI=1/C31H62N6O4.C2H4O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-31(41)35-21-25-37(24-20-30(34)40)27-26-36(22-18-28(32)38)23-19-29(33)39;1-2(3)4/h2-27H2,1H3,(H2,32,38)(H2,33,39)(H2,34,40)(H,35,41);1H3,(H,3,4)

Property Name	Value
Molecular Formula	C31H62N6O4
Molecular Weight	642.5
AlogP	7.68
Hydrogen Bond Acceptor	7.0
Hydrogen Bond Donor	8.0
Number of Rotational Bond	31.0
Polar Surface Area	208.61
Heavy Atoms	45.0

Property Name

Value

Molecular Formula

C31H62N6O4

Molecular Weight

642.5

AlogP

7.68

Hydrogen Bond Acceptor

7.0

Hydrogen Bond Donor

8.0

Number of Rotational Bond

31.0

Polar Surface Area

208.61

Heavy Atoms

45.0

Resources	Reference
CAS NUMBER	68214-48-2
NORMAN SUSDAT
PubChem	109770

Resources

Reference

CAS NUMBER

68214-48-2

NORMAN SUSDAT

PubChem

109770

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...

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Last update: Monday, 3 November 2025

N-[2-[(3-AMINO-3-OXOPROPYL)[2-[BIS(3-AMINO-3-OXOPROPYL)AMINO]ETHYL]AMINO]ETHYL]STEARAMIDE MONOACETATE

Structure

Physicochemical Descriptors

Cross References