EcoDrugPlus


Synonyms	Comfosy Epicyn hydrogel Hypochlorous acid
Status
Molecule Category	UNKNOWN
UNII	712K4CDC10
EPA CompTox	DTXSID3036737

Synonyms

Comfosy

Epicyn hydrogel

Hypochlorous acid

Status

Molecule Category

UNKNOWN

UNII

712K4CDC10

EPA CompTox

DTXSID3036737


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


InChI Key	QWPPOHNGKGFGJK-UHFFFAOYSA-N
Smiles	OCl
InChI	InChI=1S/ClHO/c1-2/h2H

InChI Key

QWPPOHNGKGFGJK-UHFFFAOYSA-N

Smiles

OCl

InChI

InChI=1S/ClHO/c1-2/h2H

Property Name	Value
Molecular Formula	HClO
Molecular Weight	52.46
AlogP	0.13
Hydrogen Bond Acceptor	1.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	0.0
Polar Surface Area	20.23
Molecular species	NEUTRAL
Aromatic Rings	0.0
Heavy Atoms	2.0

Property Name

Value

Molecular Formula

HClO

Molecular Weight

52.46

AlogP

0.13

Hydrogen Bond Acceptor

1.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

0.0

Polar Surface Area

20.23

Molecular species

NEUTRAL

Aromatic Rings

0.0

Heavy Atoms

2.0

Resources	Reference
ChEBI	24757
ChEMBL	CHEMBL1616046
DrugBank	DB14135
FDA SRS	712K4CDC10
Human Metabolome Database	HMDB0059650
PDB	8TR
PubChem	24341
SureChEMBL	SCHEMBL15644

Resources

Reference

ChEBI

ChEMBL

DrugBank

FDA SRS

Human Metabolome Database

PDB

PubChem

SureChEMBL


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).

HYPOCHLOROUS ACID

Structure

Physicochemical Descriptors

Cross References