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Details

Stereochemistry ACHIRAL
Molecular Formula Co
Molecular Weight 58.9332
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 2

SHOW SMILES / InChI
Structure of COBALTOUS CATION

SMILES

[Co++]

InChI

InChIKey=XLJKHNWPARRRJB-UHFFFAOYSA-N
InChI=1S/Co/q+2

HIDE SMILES / InChI

Molecular Formula Co
Molecular Weight 58.9332
Charge 2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q9NWT6
Gene ID: 55662.0
Gene Symbol: HIF1AN
Target Organism: Homo sapiens (Human)
1.0 µM [Ki]
Conditions
PubMed

PubMed

TitleDatePubMed
Cobalt iontophoresis techniques for tracing afferent and efferent connections in the vertebrate CNS.
1975 May 2
Improved methods for cobalt filling and silver intensification of insect motor neurons.
1982 Jul
Acute oral toxicity of inorganic cobalt compounds in rats.
1982 Jun
Inhalation toxicity studies of cobalt sulfate in F344/N rats and B6C3F1 mice.
1990 Aug
Carcinogenic sulfide salts of nickel and cadmium induce H2O2 formation by human polymorphonuclear leukocytes.
1990 Dec 1
Synthesis and Anti-Candida Activity of Cobalt(II) Complexes of Benzene-1,2-Dioxyacetic Acid (bdoaH(2)). X-Ray Crystal Structures of [Co(bdoa)(H(2)O)(3)] 3.5H(2)O and {[CO(phen)(3)](bdoa)}(2)24H(2)O (phen = 1,10-Phenanthroline).
1999
Determination of trace metal ions in common salt by stripping voltammetry.
1999 Nov-Dec
Cobalt and antimony: genotoxicity and carcinogenicity.
2003 Dec 10
Synthesis and antifungal potential of Co(II) complexes of 1-(2'-hydroxyphenyl) ethylideneanilines.
2006 Feb
In vitro assessment of cobalt oxide particle toxicity: identifying and circumventing interference.
2013 Sep
In vitro evaluation of anticancer and antibacterial activities of cobalt oxide nanoparticles.
2015 Dec
Purification and characterization of glucose 6-phosphate dehydrogenase enzyme from rainbow trout (Oncorhynchus mykiss) liver and investigation of the effects of some metal ions on enzyme activity.
2015 May
Differential pulmonary effects of CoO and La2O3 metal oxide nanoparticle responses during aerosolized inhalation in mice.
2016 Aug 15
Patents

Sample Use Guides

In Vivo Use Guide
For treatment of anemia, oral cobal chloride was administered at doses 25 mg and 50 mg daily.
Route of Administration: Oral
HIF asparaginyl hydroxylase activity was measured by a method based on the hydroxylation coupled decarboxylation of 2-oxoglutarate with the synthetic HIF-1α peptides in the presence of varying concentrations of Co (1-5 uM). Ki for HIF asparaginyl hydroxylase was 1uM.
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:48:34 UTC 2023
Edited
by admin
on Fri Dec 15 18:48:34 UTC 2023
Record UNII
AI1MR454XG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
COBALTOUS CATION
Common Name English
CO2+
Common Name English
COBALT(II) CATION
Common Name English
COBALT CATION (CO2+)
Common Name English
COBALT(II) ION
Common Name English
COBALTOUS ION
Common Name English
COBALT, ION (CO2+)
Common Name English
COBALT(2+)
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C68247
Created by admin on Fri Dec 15 18:48:35 UTC 2023 , Edited by admin on Fri Dec 15 18:48:35 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID20177066
Created by admin on Fri Dec 15 18:48:35 UTC 2023 , Edited by admin on Fri Dec 15 18:48:35 UTC 2023
PRIMARY
DAILYMED
AI1MR454XG
Created by admin on Fri Dec 15 18:48:35 UTC 2023 , Edited by admin on Fri Dec 15 18:48:35 UTC 2023
PRIMARY
NCI_THESAURUS
C68248
Created by admin on Fri Dec 15 18:48:35 UTC 2023 , Edited by admin on Fri Dec 15 18:48:35 UTC 2023
PRIMARY
CAS
22541-53-3
Created by admin on Fri Dec 15 18:48:35 UTC 2023 , Edited by admin on Fri Dec 15 18:48:35 UTC 2023
PRIMARY
RXCUI
1546419
Created by admin on Fri Dec 15 18:48:35 UTC 2023 , Edited by admin on Fri Dec 15 18:48:35 UTC 2023
PRIMARY RxNorm
PUBCHEM
104729
Created by admin on Fri Dec 15 18:48:35 UTC 2023 , Edited by admin on Fri Dec 15 18:48:35 UTC 2023
PRIMARY
DRUG BANK
DB14205
Created by admin on Fri Dec 15 18:48:35 UTC 2023 , Edited by admin on Fri Dec 15 18:48:35 UTC 2023
PRIMARY
FDA UNII
AI1MR454XG
Created by admin on Fri Dec 15 18:48:35 UTC 2023 , Edited by admin on Fri Dec 15 18:48:35 UTC 2023
PRIMARY
CHEBI
48828
Created by admin on Fri Dec 15 18:48:35 UTC 2023 , Edited by admin on Fri Dec 15 18:48:35 UTC 2023
PRIMARY
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