EcoDrugPlus


Synonyms	Fluoride
Status
Molecule Category	Free-form
UNII	RGL5YE86CZ
EPA CompTox	DTXSID1049641
Parent Compound:	FLUORIDE

Synonyms

Fluoride

Status

Molecule Category

Free-form

UNII

RGL5YE86CZ

EPA CompTox

DTXSID1049641

Parent Compound:

FLUORIDE


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


InChI Key	KRHYYFGTRYWZRS-UHFFFAOYSA-N
Smiles	F
InChI	InChI=1S/FH/h1H

InChI Key

KRHYYFGTRYWZRS-UHFFFAOYSA-N

Smiles

InChI

InChI=1S/FH/h1H

Property Name	Value
Molecular Formula	HF
Molecular Weight	20.01
AlogP	0.15
Hydrogen Bond Acceptor	0.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	0.0
Polar Surface Area	0.0
Molecular species	ACID
Aromatic Rings	0.0
Heavy Atoms	1.0

Property Name

Value

Molecular Formula

Molecular Weight

20.01

AlogP

0.15

Hydrogen Bond Acceptor

0.0

Hydrogen Bond Donor

0.0

Number of Rotational Bond

0.0

Polar Surface Area

0.0

Molecular species

ACID

Aromatic Rings

0.0

Heavy Atoms

1.0

Resources	Reference
ChEBI	29228
ChEMBL	CHEMBL1232767
DrugBank	DB11072
DrugCentral	4499
FDA SRS	RGL5YE86CZ
KEGG	C16487
SureChEMBL	SCHEMBL630

Resources

Reference

ChEBI

ChEMBL

DrugBank

DrugCentral

FDA SRS

KEGG

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).

FLUORIDE

Structure

Physicochemical Descriptors

Cross References