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Compound Detail

CHEMBL1200679

ZINC CHLORIDE
💊 Approved Drug
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💊 Approved Drug
[Cl-].[Cl-].[Zn+2]

Basic Information

ChEMBL ID CHEMBL1200679
Name ZINC CHLORIDE
Phase Approved
Structure Type MOL
InChI Key JIAARYAFYJHUJI-UHFFFAOYSA-L

Known Names

NSC-529648 Zinc chloride Zincum muriaticum
9
Targets
11
Activities
4
Assay Types
0
PK Parameters
8
Publications
3
Known Names

Molecular Properties

136.3
MW (Da)

Drug Information

Molecule Type Small molecule
First Approval 1986
Availability Prescription
Chirality Achiral

Routes of Administration

Parenteral

Extended Properties

Molecular Formula Cl2Zn
MW 136.30

ATC Classification

B05XA12
zinc chloride
Level 1: BLOOD AND BLOOD FORMING ORGANS
Level 2: BLOOD SUBSTITUTES AND PERFUSION SOLUTIONS

Activity Summary

IC50 6 meas. best 5.96
EC50 2 meas. best 8.44
Ki 2 meas. best 5.36
Kd 1 meas. best 4.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
G-protein coupled receptor 39
CHEMBL3091266
EC50 8.44 8.44 3.6 1
Protein phosphatase 3 catalytic subunit alpha
CHEMBL4445
IC50 5.96 5.96 1100.3 1
Carbonic anhydrase 2
CHEMBL205
IC50 5.94 5.94 1159.0 1
Tyrosine-protein kinase Fyn
CHEMBL1841
IC50 5.73 5.73 1877.9 1
Epidermal growth factor receptor
CHEMBL203
IC50 5.66 5.66 2188.4 1
Protein Gpr39
CHEMBL3091267
EC50 5.39 5.39 4038.0 1
Androgen receptor
CHEMBL3072
Ki 5.36 5.36 4339.1 1
Androgen receptor
CHEMBL3072
IC50 5.19 5.19 6508.6 1
Sodium-dependent noradrenaline transporter
CHEMBL222
Ki 5.16 5.16 6950.4 1
Sodium-dependent noradrenaline transporter
CHEMBL222
IC50 5.15 5.15 7008.3 1
Ubiquitin-conjugating enzyme E2 T
CHEMBL4105763
Kd 4.8 4.8 15700.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
G-protein coupled receptor 39 EC50 = 3.6 nM 8.44 Agonist activity at human GPR39 expressed in HEK293 cells by cAMP assay 25313322
Protein phosphatase 3 catalytic subunit alpha IC50 = 1100.3 nM 5.96 DRUGMATRIX: Protein Serine/Threonine Phosphatase, PPP3CA (Calcineurin, PP2B) enz... -
Carbonic anhydrase 2 IC50 = 1159.0 nM 5.94 DRUGMATRIX: Carbonic Anhydrase II enzyme inhibition (substrate: 4-Nitrophenyl ac... -
Tyrosine-protein kinase Fyn IC50 = 1877.9 nM 5.73 DRUGMATRIX: Protein Tyrosine Kinase, Fyn enzyme inhibition (substrate: Poly(Glu:... -
Epidermal growth factor receptor IC50 = 2188.4 nM 5.66 DRUGMATRIX: Protein Tyrosine Kinase, EGF Receptor enzyme inhibition (substrate: ... -
Protein Gpr39 EC50 = 4038.0 nM 5.39 Agonist activity at rat GPR39 expressed in HEK293 cells by IP1 assay 25313322
Androgen receptor Ki = 4339.1 nM 5.36 DRUGMATRIX: Androgen (Testosterone) AR radioligand binding (ligand: [3H] Miboler... -
Androgen receptor IC50 = 6508.6 nM 5.19 DRUGMATRIX: Androgen (Testosterone) AR radioligand binding (ligand: [3H] Miboler... -
Sodium-dependent noradrenaline transporter Ki = 6950.4 nM 5.16 DRUGMATRIX: Norepinephrine Transporter radioligand binding (ligand: [125I] RTI-5... -
Sodium-dependent noradrenaline transporter IC50 = 7008.3 nM 5.15 DRUGMATRIX: Norepinephrine Transporter radioligand binding (ligand: [125I] RTI-5... -
Ubiquitin-conjugating enzyme E2 T Kd = 15700.0 nM 4.8 Binding affinity to N-terminally 6xHis-Smt3 tagged human Ube2T C86K/K91R/K95R mu... 28933844

Literature References

PubMed DOI Target Context # Activities
37466499 10.1021/acs.jmedchem.3c00368 Staphylococcus aureus 8
25313322 10.1021/ml500240d G-protein coupled receptor 39 2
25313322 10.1021/ml500240d Unchecked 2
25313322 10.1021/ml500240d Protein Gpr39 1
25313322 10.1021/ml500240d NON-PROTEIN TARGET 1
28933844 10.1021/acs.jmedchem.7b01071 Ubiquitin-conjugating enzyme E2 T 1
32619886 10.1016/j.ejmech.2020.112522 NCI-H3255 1
37466499 10.1021/acs.jmedchem.3c00368 Escherichia coli 1

Data from ChEMBL 36 via Core Engine