EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID70998182

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID70998182


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70


InChI Key	ULWSOHSPXPGMRN-UHFFFAOYSA-N
Smiles	N#CC(C#N)=CC1=CC=C(C=C1C)N(C)CCCCCCN(C2=CC=C(C=C(C#N)C#N)C(=C2)C)CC
InChI	InChI=1/C31H34N6/c1-5-37(31-13-11-29(25(3)17-31)19-27(22-34)23-35)15-9-7-6-8-14-36(4)30-12-10-28(24(2)16-30)18-26(20-32)21-33/h10-13,16-19H,5-9,14-15H2,1-4H3

InChI Key

ULWSOHSPXPGMRN-UHFFFAOYSA-N

Smiles

N#CC(C#N)=CC1=CC=C(C=C1C)N(C)CCCCCCN(C2=CC=C(C=C(C#N)C#N)C(=C2)C)CC

InChI

InChI=1/C31H34N6/c1-5-37(31-13-11-29(25(3)17-31)19-27(22-34)23-35)15-9-7-6-8-14-36(4)30-12-10-28(24(2)16-30)18-26(20-32)21-33/h10-13,16-19H,5-9,14-15H2,1-4H3

Property Name	Value
Molecular Formula	C31H34N6
Molecular Weight	490.28
AlogP	6.69
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	12.0
Polar Surface Area	101.64
Molecular species	None
Aromatic Rings	2.0
Heavy Atoms	37.0

Property Name

Value

Molecular Formula

C31H34N6

Molecular Weight

490.28

AlogP

6.69

Hydrogen Bond Acceptor

6.0

Hydrogen Bond Donor

0.0

Number of Rotational Bond

12.0

Polar Surface Area

101.64

Molecular species

None

Aromatic Rings

2.0

Heavy Atoms

37.0

Resources	Reference
CAS NUMBER	76897-80-8
NORMAN SUSDAT
PubChem	21149569

Resources

Reference

CAS NUMBER

76897-80-8

NORMAN SUSDAT

PubChem

21149569


PREMIER has received funding from the 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 this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the 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 this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

[[4-[[6-[[4-(2,2-DICYANOVINYL)-3-METHYLPHENYL]ETHYLAMINO]HEXYL]METHYLAMINO]-2-METHYLPHENYL]METHYLENE]MALONONITRILE

Structure

Physicochemical Descriptors

Cross References