EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Salt-form
EPA CompTox	DTXSID60200049

Keyword(s):

Human Metabolites

Molecule Category

Salt-form

EPA CompTox

DTXSID60200049


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


InChI Key	OVNUPJXMCMTQCN-UHFFFAOYSA-N
Smiles	Cl.O(C1=CC=C(C=C1)NN)CC=2C=CC=CC2
InChI	InChI=1/C13H14N2O.ClH/c14-15-12-6-8-13(9-7-12)16-10-11-4-2-1-3-5-11;/h1-9,15H,10,14H2;1H

InChI Key

OVNUPJXMCMTQCN-UHFFFAOYSA-N

Smiles

Cl.O(C1=CC=C(C=C1)NN)CC=2C=CC=CC2

InChI

InChI=1/C13H14N2O.ClH/c14-15-12-6-8-13(9-7-12)16-10-11-4-2-1-3-5-11;/h1-9,15H,10,14H2;1H

Property Name	Value
Molecular Formula	C13H14N2O
Molecular Weight	250.09
AlogP	2.97
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	4.0
Polar Surface Area	47.28
Molecular species	None
Aromatic Rings	2.0
Heavy Atoms	17.0

Property Name

Value

Molecular Formula

C13H14N2O

Molecular Weight

250.09

AlogP

2.97

Hydrogen Bond Acceptor

3.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

4.0

Polar Surface Area

47.28

Molecular species

None

Aromatic Rings

2.0

Heavy Atoms

17.0

Resources	Reference
CAS NUMBER	52068-30-1
NORMAN SUSDAT
PubChem	561392

Resources

Reference

CAS NUMBER

52068-30-1

NORMAN SUSDAT

PubChem

561392


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-(BENZYLOXY)PHENYL]HYDRAZINE MONOHYDROCHLORIDE

Structure

Physicochemical Descriptors

Cross References