2,2':6',2''-Terpyridine Platinum(Ii)

Identification

Generic Name
2,2':6',2''-Terpyridine Platinum(Ii)
DrugBank Accession Number
DB01912
Background

2,2':6',2''-terpyridine Platinum(Ii) is a solid. Known drug targets of 2,2':6',2''-Terpyridine Platinum(Ii) include truncated transposase and autolysin.

Type
Small Molecule
Groups
Experimental
Structure
Weight
Average: 463.805
Monoisotopic: 463.028924523
Chemical Formula
C15H11ClN3Pt
Synonyms
Not Available

Pharmacology

Indication

Not Available

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Pharmacodynamics

Not Available

Mechanism of action
TargetActionsOrganism
UAutolysinNot AvailableStreptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4)
UTruncated transposaseNot AvailableEscherichia coli
Absorption

Not Available

Volume of distribution

Not Available

Protein binding

Not Available

Metabolism
Not Available
Route of elimination

Not Available

Half-life

Not Available

Clearance

Not Available

Adverse Effects
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Toxicity

Not Available

Pathways
Not Available
Pharmacogenomic Effects/ADRs
Not Available

Interactions

Drug Interactions
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Not Available
Food Interactions
Not Available

Categories

Drug Categories
Not Available
Classification
Not classified
Affected organisms
Not Available

Chemical Identifiers

UNII
Not Available
CAS number
Not Available
InChI Key
XTQMQLRZXBEQCS-UHFFFAOYSA-M
InChI
InChI=1S/C15H11N3.ClH.Pt/c1-3-10-16-12(6-1)14-8-5-9-15(18-14)13-7-2-4-11-17-13;;/h1-11H;1H;/q;;+2/p-1
IUPAC Name
platinum(2+) 6-(pyridin-2-yl)-2,2'-bipyridine chloride
SMILES
[Cl-].[Pt++].C1=CC=C(N=C1)C1=CC=CC(=N1)C1=CC=CC=N1

References

General References
Not Available
PubChem Compound
124734
PubChem Substance
46507377
ChemSpider
111059
PDBe Ligand
TPT
PDB Entries
1b7e / 1hcx / 1qnq / 2zzb / 3ro0 / 3ro1

Clinical Trials

Clinical Trials
PhaseStatusPurposeConditionsCount

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
Not Available
Prices
Not Available
Patents
Not Available

Properties

State
Solid
Experimental Properties
Not Available
Predicted Properties
PropertyValueSource
Water Solubility0.129 mg/mLALOGPS
logP2.78ALOGPS
logP3.16Chemaxon
logS-3.3ALOGPS
pKa (Strongest Basic)3.26Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count3Chemaxon
Hydrogen Donor Count0Chemaxon
Polar Surface Area38.67 Å2Chemaxon
Rotatable Bond Count2Chemaxon
Refractivity68.37 m3·mol-1Chemaxon
Polarizability25.56 Å3Chemaxon
Number of Rings3Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleYesChemaxon
MDDR-like RuleNoChemaxon
Predicted ADMET Features
PropertyValueProbability
Human Intestinal Absorption+0.9924
Blood Brain Barrier+0.9738
Caco-2 permeable+0.5221
P-glycoprotein substrateSubstrate0.5219
P-glycoprotein inhibitor INon-inhibitor0.732
P-glycoprotein inhibitor IINon-inhibitor0.9031
Renal organic cation transporterInhibitor0.6951
CYP450 2C9 substrateNon-substrate0.8612
CYP450 2D6 substrateNon-substrate0.6332
CYP450 3A4 substrateNon-substrate0.6513
CYP450 1A2 substrateNon-inhibitor0.6556
CYP450 2C9 inhibitorNon-inhibitor0.897
CYP450 2D6 inhibitorNon-inhibitor0.8627
CYP450 2C19 inhibitorNon-inhibitor0.8356
CYP450 3A4 inhibitorNon-inhibitor0.9592
CYP450 inhibitory promiscuityLow CYP Inhibitory Promiscuity0.7069
Ames testNon AMES toxic0.5
CarcinogenicityNon-carcinogens0.9437
BiodegradationNot ready biodegradable1.0
Rat acute toxicity2.3812 LD50, mol/kg Not applicable
hERG inhibition (predictor I)Strong inhibitor0.6917
hERG inhibition (predictor II)Non-inhibitor0.8198
ADMET data is predicted using admetSAR, a free tool for evaluating chemical ADMET properties. (23092397)

Spectra

Mass Spec (NIST)
Not Available
Spectra
Not Available
Chromatographic Properties
Collision Cross Sections (CCS)
Not Available

Targets

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Kind
Protein
Organism
Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4)
Pharmacological action
Unknown
General Function
N-acetylmuramoyl-l-alanine amidase activity
Specific Function
Autolysins are involved in some important biological processes such as cell separation, cell-wall turnover, competence for genetic transformation, formation of the flagella and sporulation. Autolys...
Gene Name
lytA
Uniprot ID
P06653
Uniprot Name
Autolysin
Molecular Weight
36544.235 Da
References
  1. Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. [Article]
  2. Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. [Article]
Kind
Protein
Organism
Escherichia coli
Pharmacological action
Unknown
General Function
Transposase activity
Specific Function
Not Available
Gene Name
tnp
Uniprot ID
Q46730
Uniprot Name
Transposase
Molecular Weight
50490.335 Da

Drug created at June 13, 2005 13:24 / Updated at June 12, 2020 16:52