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IOX2 - ≥98%, high purity , CAS No.931398-72-0, Inhibitor of egl-9 family hypoxia inducible factor 1;Inhibitor of lysine demethylase 2A;Inhibitor of lysine demethylase 5C

In stock
Item Number
I127127
Grouped product items
SKU Size
Availability
Price Qty
I127127-5mg
5mg
3
$98.90
I127127-25mg
25mg
2
$445.90
I127127-100mg
100mg
2
$1,603.90

Potent, cell-permeable, selective HIF-1α prolyl hydroxylase-2 (PHD2) inhibitor

Basic Description

Synonyms BCP06141 | sodium (1-benzyl-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carbonyl)glycinate | NCGC00344625-13 | EX-A099 | HMS3426G15 | NCGC00344625-02 | CHEBI:95087 | FT-0746473 | IOX2, >=98% (HPLC) | AKOS024458165 | N-[[1,2-Dihydro-4-hydroxy-2-oxo-1-(phenylmet
Specifications & Purity Moligand™, ≥98%
Biochemical and Physiological Mechanisms IOX2 is selective and potent inhibitor of prolyl hydroxylases (PHD). Stabilization of HIF-1R through inhibition of PHD has been examined as a potential treatment for ischemic diseases including anemia, myocardial infarction, and stroke. IOX2 is a selectiv
Storage Temp Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Moligand™
Action Type INHIBITOR
Mechanism of action Inhibitor of egl-9 family hypoxia inducible factor 1;Inhibitor of lysine demethylase 2A;Inhibitor of lysine demethylase 5C
Note Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

IOX2 is a potent inhibitor of HIF-1α prolyl hydroxylase-2 (PHD2) with IC50 of 21 nM in a cell-free assay, >100-fold selectivity over JMJD2A, JMJD2C, JMJD2E, JMJD3, or the 2OG oxygenase FIH.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Quinolines and derivatives
Subclass 1-benzylquinolines
Intermediate Tree Nodes Not available
Direct Parent 1-benzylquinolines
Alternative Parents Quinoline-3-carboxamides  N-acyl-alpha amino acids  Hydroquinolones  Hydroxyquinolines  Hydroquinolines  Pyridinecarboxylic acids and derivatives  Pyridinones  Hydroxypyridines  Benzene and substituted derivatives  Vinylogous amides  Vinylogous acids  Heteroaromatic compounds  Secondary carboxylic acid amides  Lactams  Azacyclic compounds  Carboxylic acids  Monocarboxylic acids and derivatives  Organonitrogen compounds  Organopnictogen compounds  Hydrocarbon derivatives  Organic oxides  Carbonyl compounds  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents 1-benzylquinoline - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Quinoline-3-carboxamide - Dihydroquinolone - Hydroxyquinoline - Alpha-amino acid or derivatives - Dihydroquinoline - Pyridine carboxylic acid or derivatives - Hydroxypyridine - Pyridinone - Benzenoid - Pyridine - Monocyclic benzene moiety - Vinylogous acid - Heteroaromatic compound - Vinylogous amide - Secondary carboxylic acid amide - Carboxamide group - Lactam - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as 1-benzylquinolines. These are organic aromatic compounds containing a quinoline that is substituted at the 1-position by a benzyl group.
External Descriptors Not available

Associated Targets(Human)

EGLN1 Tclin Egl nine homolog 1 (3 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
KDM5C Tchem Lysine-specific demethylase 5C (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
KDM2A Tchem Lysine-specific demethylase 2A (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
EGLN1 Tclin Egl nine homolog 1 (1702 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 2-[(1-benzyl-4-hydroxy-2-oxoquinoline-3-carbonyl)amino]acetic acid
INCHI InChI=1S/C19H16N2O5/c22-15(23)10-20-18(25)16-17(24)13-8-4-5-9-14(13)21(19(16)26)11-12-6-2-1-3-7-12/h1-9,24H,10-11H2,(H,20,25)(H,22,23)
InChIKey CAOSCCRYLYQBES-UHFFFAOYSA-N
Smiles C1=CC=C(C=C1)CN2C3=CC=CC=C3C(=C(C2=O)C(=O)NCC(=O)O)O
Isomeric SMILES C1=CC=C(C=C1)CN2C3=CC=CC=C3C(=C(C2=O)C(=O)NCC(=O)O)O
WGK Germany 3
Molecular Weight 352.34
Reaxy-Rn 12851765
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=12851765&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot Number Certificate Type Date Item
E1705098 Certificate of Analysis Sep 11, 2024 I127127
L2326038 Certificate of Analysis Jan 03, 2024 I127127

Chemical and Physical Properties

Solubility DMSO 100 mg/ml
Molecular Weight 352.300 g/mol
XLogP3 2.600
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 5
Exact Mass 352.106 Da
Monoisotopic Mass 352.106 Da
Topological Polar Surface Area 107.000 Ų
Heavy Atom Count 26
Formal Charge 0
Complexity 609.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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