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Veliparib

CAS No.:
912444-00-9
Catalog Number:
AG0039KX
Molecular Formula:
C13H16N4O
Molecular Weight:
244.2923
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1mg
98%(HPLC)
In Stock USA
United States
$53
- +
5mg
98%(HPLC)
In Stock USA
United States
$86
- +
10mg
98%(HPLC)
In Stock USA
United States
$136
- +
50mg
98%(HPLC)
In Stock USA
United States
$353
- +
100mg
98%(HPLC)
In Stock USA
United States
$553
- +
Product Description
Catalog Number:
AG0039KX
Chemical Name:
Veliparib
CAS Number:
912444-00-9
Molecular Formula:
C13H16N4O
Molecular Weight:
244.2923
MDL Number:
MFCD16661059
IUPAC Name:
2-[(2R)-2-methylpyrrolidin-2-yl]-1H-benzimidazole-4-carboxamide
InChI:
InChI=1S/C13H16N4O/c1-13(6-3-7-15-13)12-16-9-5-2-4-8(11(14)18)10(9)17-12/h2,4-5,15H,3,6-7H2,1H3,(H2,14,18)(H,16,17)/t13-/m1/s1
InChI Key:
JNAHVYVRKWKWKQ-CYBMUJFWSA-N
SMILES:
NC(=O)c1cccc2c1[nH]c(n2)[C@@]1(C)CCCN1
UNII:
01O4K0631N
NSC Number:
737664
Properties
Complexity:
348  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
244.132g/mol
Formal Charge:
0
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
244.298g/mol
Monoisotopic Mass:
244.132g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
83.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5  
Literature
Title Journal
Analyzing structure-function relationships of artificial and cancer-associated PARP1 variants by reconstituting TALEN-generated HeLa PARP1 knock-out cells. Nucleic acids research 20161201
CDK12 Inhibition Reverses De Novo and Acquired PARP Inhibitor Resistance in BRCA Wild-Type and Mutated Models of Triple-Negative Breast Cancer. Cell reports 20161122
Adaptive Randomization of Veliparib-Carboplatin Treatment in Breast Cancer. The New England journal of medicine 20160707
Sulfur and nitrogen mustards induce characteristic poly(ADP-ribosyl)ation responses in HaCaT keratinocytes with distinctive cellular consequences. Toxicology letters 20160226
Discovery of 2-[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-6-fluoro-3-oxo-2,3-dihydro-1H-isoindole-4-carboxamide (NMS-P118): A Potent, Orally Available, and Highly Selective PARP-1 Inhibitor for Cancer Therapy. Journal of medicinal chemistry 20150910
Mitochondrial reactive oxygen species are scavenged by Cockayne syndrome B protein in human fibroblasts without nuclear DNA damage. Proceedings of the National Academy of Sciences of the United States of America 20140916
Pharmacological Inhibition of poly(ADP-ribose) polymerases improves fitness and mitochondrial function in skeletal muscle. Cell metabolism 20140603
Identification of potent Yes1 kinase inhibitors using a library screening approach. Bioorganic & medicinal chemistry letters 20130801
Identification of DNA repair pathways that affect the survival of ovarian cancer cells treated with a poly(ADP-ribose) polymerase inhibitor in a novel drug combination. Molecular pharmacology 20121001
Poly(ADP-ribose) polymerase 1 modulates the lethality of CHK1 inhibitors in mammary tumors. Molecular pharmacology 20120801
Radiation-inducible immunotherapy for cancer: senescent tumor cells as a cancer vaccine. Molecular therapy : the journal of the American Society of Gene Therapy 20120501
Poly(ADP-ribose) polymerase 1 inhibition improves coronary arteriole function in type 2 diabetes mellitus. Hypertension (Dallas, Tex. : 1979) 20120501
Failure of iniparib to inhibit poly(ADP-Ribose) polymerase in vitro. Clinical cancer research : an official journal of the American Association for Cancer Research 20120315
A phase I study of veliparib in combination with metronomic cyclophosphamide in adults with refractory solid tumors and lymphomas. Clinical cancer research : an official journal of the American Association for Cancer Research 20120315
The impact of cyclin-dependent kinase 5 depletion on poly(ADP-ribose) polymerase activity and responses to radiation. Cellular and molecular life sciences : CMLS 20120301
Enhanced killing of cancer cells by poly(ADP-ribose) polymerase inhibitors and topoisomerase I inhibitors reflects poisoning of both enzymes. The Journal of biological chemistry 20120203
Iniparib nonselectively modifies cysteine-containing proteins in tumor cells and is not a bona fide PARP inhibitor. Clinical cancer research : an official journal of the American Association for Cancer Research 20120115
Novel binding mode of a potent and selective tankyrase inhibitor. PloS one 20120101
Synthetic lethal interactions between EGFR and PARP inhibition in human triple negative breast cancer cells. PloS one 20120101
Bortezomib-induced 'BRCAness' sensitizes multiple myeloma cells to PARP inhibitors. Blood 20111208
Poly(ADP-ribose) polymerase inhibition enhances p53-dependent and -independent DNA damage responses induced by DNA damaging agent. Cell cycle (Georgetown, Tex.) 20111201
Anti-estrogen resistance in breast cancer is induced by the tumor microenvironment and can be overcome by inhibiting mitochondrial function in epithelial cancer cells. Cancer biology & therapy 20111115
Veliparib plus temozolomide in metastatic melanoma trends toward increased PFS but results are not statistically significant. Oncology (Williston Park, N.Y.) 20111115
Poly(ADP-ribose) polymerase inhibitors combined with external beam and radioimmunotherapy to treat aggressive lymphoma. Nuclear medicine communications 20111101
Response of subtype-specific human breast cancer-derived cells to poly(ADP-ribose) polymerase and checkpoint kinase 1 inhibition. Cancer science 20111001
Phase I study of PARP inhibitor ABT-888 in combination with topotecan in adults with refractory solid tumors and lymphomas. Cancer research 20110901
Poly(ADP-Ribose) polymerase inhibition synergizes with 5-fluorodeoxyuridine but not 5-fluorouracil in ovarian cancer cells. Cancer research 20110715
Disposition and drug-drug interaction potential of veliparib (ABT-888), a novel and potent inhibitor of poly(ADP-ribose) polymerase. Drug metabolism and disposition: the biological fate of chemicals 20110701
Response of human prostate cancer cells and tumors to combining PARP inhibition with ionizing radiation. Molecular cancer therapeutics 20110701
Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies. The Journal of clinical investigation 20110701
PARP inhibitors: its role in treatment of cancer. Chinese journal of cancer 20110701
The poly(ADP-Ribose) polymerase inhibitor ABT-888 reduces radiation-induced nuclear EGFR and augments head and neck tumor response to radiotherapy. Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology 20110601
Poly(ADP-ribose) polymerase and XPF-ERCC1 participate in distinct pathways for the repair of topoisomerase I-induced DNA damage in mammalian cells. Nucleic acids research 20110501
N-methylpurine DNA glycosylase and DNA polymerase beta modulate BER inhibitor potentiation of glioma cells to temozolomide. Neuro-oncology 20110501
5-Benzamidoisoquinolin-1-ones and 5-(ω-carboxyalkyl)isoquinolin-1-ones as isoform-selective inhibitors of poly(ADP-ribose) polymerase 2 (PARP-2). Journal of medicinal chemistry 20110414
MRE11 deficiency increases sensitivity to poly(ADP-ribose) polymerase inhibition in microsatellite unstable colorectal cancers. Cancer research 20110401
PARP inhibitors in oncology: a new synthetic lethal approach to cancer therapy. Acta clinica Belgica 20110101
Cetuximab augments cytotoxicity with poly (adp-ribose) polymerase inhibition in head and neck cancer. PloS one 20110101
Modeling pharmacodynamic response to the poly(ADP-Ribose) polymerase inhibitor ABT-888 in human peripheral blood mononuclear cells. PloS one 20110101
Cooperation of breast cancer proteins PALB2 and piccolo BRCA2 in stimulating homologous recombination. Nature structural & molecular biology 20101001
Poly(ADP-ribose) polymerase inhibitor induces accelerated senescence in irradiated breast cancer cells and tumors. Cancer research 20100801
PTEN loss compromises homologous recombination repair in astrocytes: implications for glioblastoma therapy with temozolomide or poly(ADP-ribose) polymerase inhibitors. Cancer research 20100701
A rapid and sensitive method for determination of veliparib (ABT-888), in human plasma, bone marrow cells and supernatant by using LC/MS/MS. Journal of pharmaceutical and biomedical analysis 20100501
Crystal structure of the catalytic domain of human PARP2 in complex with PARP inhibitor ABT-888. Biochemistry 20100216
Plasma and cerebrospinal fluid pharmacokinetics of ABT-888 after oral administration in non-human primates. Cancer chemotherapy and pharmacology 20100201
Simultaneous determination of ABT-888, a poly (ADP-ribose) polymerase inhibitor, and its metabolite in human plasma by liquid chromatography/tandem mass spectrometry. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20100201
Poly(adp-ribose) polymerase inhibitors: a novel drug class with a promising future. Cancer journal (Sudbury, Mass.) 20100101
Emergence of rationally designed therapeutic strategies for breast cancer targeting DNA repair mechanisms. Breast cancer research : BCR 20100101
ABT-888 confers broad in vivo activity in combination with temozolomide in diverse tumors. Clinical cancer research : an official journal of the American Association for Cancer Research 20091201
Synthesis and evaluation of a new generation of orally efficacious benzimidazole-based poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors as anticancer agents. Journal of medicinal chemistry 20091112
Immunohistochemical detection of poly(ADP-ribose) polymerase inhibition by ABT-888 in patients with refractory solid tumors and lymphomas. Cancer biology & therapy 20091101
Role of Phase 0 trials in drug development. Future medicinal chemistry 20091101
Acquired resistance to combination treatment with temozolomide and ABT-888 is mediated by both base excision repair and homologous recombination DNA repair pathways. Molecular cancer research : MCR 20091001
Poly(ADP-ribose) polymerase inhibitor ABT-888 potentiates the cytotoxic activity of temozolomide in leukemia cells: influence of mismatch repair status and O6-methylguanine-DNA methyltransferase activity. Molecular cancer therapeutics 20090801
Phase 0 trials: a platform for drug development? Lancet (London, England) 20090718
Phase 0 clinical trials: an answer to drug development stagnation? Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20090601
Phase 0 clinical trial of the poly (ADP-ribose) polymerase inhibitor ABT-888 in patients with advanced malignancies. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 20090601
Phase 0 trials for anticancer drug development. Nature reviews. Drug discovery 20090601
Phase zero launch. Nature biotechnology 20090601
Effective sensitization of temozolomide by ABT-888 is lost with development of temozolomide resistance in glioblastoma xenograft lines. Molecular cancer therapeutics 20090201
Discovery of the Poly(ADP-ribose) polymerase (PARP) inhibitor 2-[(R)-2-methylpyrrolidin-2-yl]-1H-benzimidazole-4-carboxamide (ABT-888) for the treatment of cancer. Journal of medicinal chemistry 20090122
94th RSNA Annual Meeting. The Lancet. Oncology 20090101
Preclinical modeling of a phase 0 clinical trial: qualification of a pharmacodynamic assay of poly (ADP-ribose) polymerase in tumor biopsies of mouse xenografts. Clinical cancer research : an official journal of the American Association for Cancer Research 20081101
An enzyme-linked immunosorbent poly(ADP-ribose) polymerase biomarker assay for clinical trials of PARP inhibitors. Analytical biochemistry 20081015
Potentiation of temozolomide cytotoxicity by poly(ADP)ribose polymerase inhibitor ABT-888 requires a conversion of single-stranded DNA damages to double-stranded DNA breaks. Molecular cancer research : MCR 20081001
Liquid chromatography-mass spectrometric assay for the quantitation in human plasma of ABT-888, an orally available, small molecule inhibitor of poly(ADP-ribose) polymerase. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20080901
A novel poly(ADP-ribose) polymerase inhibitor, ABT-888, radiosensitizes malignant human cell lines under hypoxia. Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology 20080801
Phase 0 trials: an industry perspective. Clinical cancer research : an official journal of the American Association for Cancer Research 20080615
Patient perspectives on phase 0 clinical trials. Clinical cancer research : an official journal of the American Association for Cancer Research 20080615
Poly (ADP-ribose) polymerase activity regulates apoptosis in HeLa cells after alkylating DNA damage. Cancer biology & therapy 20080601
The PARP inhibitor, ABT-888 potentiates temozolomide: correlation with drug levels and reduction in PARP activity in vivo. Anticancer research 20080101
Inhibition of poly(ADP-ribose) polymerase enhances cell death and improves tumor growth delay in irradiated lung cancer models. Clinical cancer research : an official journal of the American Association for Cancer Research 20070515
ABT-888, an orally active poly(ADP-ribose) polymerase inhibitor that potentiates DNA-damaging agents in preclinical tumor models. Clinical cancer research : an official journal of the American Association for Cancer Research 20070501
Properties