E7449 - 97%, high purity , Tankyrase 1/2 inhibitor, CAS No.1140964-99-3, Tankyrase 1/2 inhibitor

  • ≥97%
Item Number
E414006
Grouped product items
SKUSizeAvailabilityPrice Qty
E414006-5mg
5mg
In stock
$141.90
E414006-10mg
10mg
In stock
$248.90
E414006-25mg
25mg
In stock
$497.90
E414006-50mg
50mg
In stock
$890.90
E414006-100mg
100mg
In stock
$1,602.90

PARP2 Selective Inhibitors

Basic Description

SynonymsHY-12418 | Parp inhibitor 2x-121 | A909458 | STENOPARIB [WHO-DD] | AC-36842 | BCP19934 | NSC783107 | NSC-783107 | NSC 6131 | 9X5A2QIA7C | 2X-121 | EX-A1282 | E7449 | E-7449 | 11-(1,3-dihydroisoindol-2-ylmethyl)-2,3,10,12-tetrazatricyclo[7.3.1.05,13]tridec
Specifications & Purity≥97%
Biochemical and Physiological MechanismsE7449 is an orally bioavailable, brain penetrable, small molecule dual inhibitor of PARP1/2 and also inhibits PARP5a/5b, otherwise known as tankyrase1 and 2 (TNKS1/2), important regulators of canonical Wnt/β-catenin signaling. It has IC50 values of 1.0 an
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Action TypeINHIBITOR
Mechanism of actionTankyrase 1/2 inhibitor
Product Description

Information

E7449 is an orally bioavailable, brain penetrable, small molecule dual inhibitor ofPARP1/2and also inhibits PARP5a/5b, otherwise known as tankyrase1 and 2 (TNKS1/2), important regulators of canonical Wnt/β-catenin signaling. It has IC50 values of 1.0 and 1.2 nM for PARP1 and 2, respectively.


Targets

PARP1 ; PARP2 1 nM; 1.2 nM


In vitro

E7449 inhibits PARP enzymatic activity and additionally traps PARP1 onto damaged DNA; a mechanism previously shown to augment cytotoxicity. E7449 inhibits Wnt/β-catenin signaling in colon cancer cell lines, likely through TNKS inhibition. E7449 stabilizes axin and TNKS proteins resulting in β-catenin de-stabilization and significantly alters expression of Wnt target genes. E7449 inhibits TNKS1 and 2 (PARP5a and 5b) with IC50 values of 50-100 nmol/L. Significant inhibitory activity is not observed for PARP3 or PARPs 6-16 (PARP9 and 13 lack activity and PARP4 had minimal signal).


In vivo

Chemotherapy is potentiated by E7449 and single agent has significant antitumor activity in BRCA-deficient xenografts. E7449 lacks single agent antitumor activity in vivo. E7449 antitumor activity is increased through combination with MEK inhibition. Treatment with E7449 at 30 or 100 mg/kg in xenografts is well-tolerated without any significant body weight loss or deaths. Treatment with E7449 at 100 mg/kg resulted in significant PARP inhibition that is sustained for at least 12 hours and recovered to basal levels within 24 h.


Cell Research(from reference)

Cell lines:Human breast cancer cell lines, HCC1143, HCC70, HCC1806, MDA-MB-436, T47D, MDA-MB-157, MDA-MB-231, MDA-MB-468, MDA-MB-453, BT-20 and Hs578T 

Incubation Time:8 days 

Product Properties

ALogP1.1

Associated Targets(Human)

TNKS Tchem Tankyrase-1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PARP1 Tclin Poly [ADP-ribose] polymerase 1 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PARP2 Tclin Poly [ADP-ribose] polymerase 2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TNKS2 Tchem Tankyrase-2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PARP1 Tclin Poly [ADP-ribose] polymerase-1 (6206 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-468 (9477 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCT-116 (91556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-231 (73002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PARP2 Tclin Poly [ADP-ribose] polymerase 2 (1185 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TNKS Tchem Tankyrase-1 (1241 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TNKS2 Tchem Tankyrase-2 (1531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TNKS2 Tchem Tankyrase 1/2 (384 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Parp2 Poly [ADP-ribose] polymerase-2 (47 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

Pubchem Sid488202973
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488202973
IUPAC Name 11-(1,3-dihydroisoindol-2-ylmethyl)-2,3,10,12-tetrazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8,11-pentaen-4-one
INCHI InChI=1S/C18H15N5O/c24-18-13-6-3-7-14-16(13)17(21-22-18)20-15(19-14)10-23-8-11-4-1-2-5-12(11)9-23/h1-7H,8-10H2,(H,22,24)(H,19,20,21)
InChi Key JLFSBHQQXIAQEC-UHFFFAOYSA-N
Canonical SMILES C1C2=CC=CC=C2CN1CC3=NC4=NNC(=O)C5=C4C(=CC=C5)N3
Isomeric SMILES C1C2=CC=CC=C2CN1CC3=NC4=NNC(=O)C5=C4C(=CC=C5)N3
PubChem CID 135565981
Molecular Weight 317.34

Certificates

Certificate of Analysis(COA)

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10 results found

Lot NumberCertificate TypeDateItem
D23061535Certificate of AnalysisFeb 11, 2023 E414006
D23061537Certificate of AnalysisFeb 11, 2023 E414006
D23061538Certificate of AnalysisFeb 11, 2023 E414006
D23061539Certificate of AnalysisFeb 11, 2023 E414006
D23061540Certificate of AnalysisFeb 11, 2023 E414006
D23061541Certificate of AnalysisFeb 11, 2023 E414006
D23061542Certificate of AnalysisFeb 11, 2023 E414006
D23061543Certificate of AnalysisFeb 11, 2023 E414006
D23061544Certificate of AnalysisFeb 11, 2023 E414006
D23061554Certificate of AnalysisFeb 11, 2023 E414006

Chemical and Physical Properties

SolubilitySolubility (25°C) In vitro DMSO: 5 mg/mL warmed with 50ºC Water: bath (15.75 mM); Water: Insoluble; Ethanol: Insoluble;

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