GLPBio

Olaparib-d 4 -1

Catalog No.: GC83754Purity:>98.50%Synonyms: AZD2281-d₄-1; KU0059436-d₄-1; MK-7339-d₄-1
Olaparib -d 4 -1 (AZD2281-d 4 -1) is the deuterium labeled Olaparib.

Les produits sont exclusivement destinés à la recherche. Ils ne doivent pas être utilisés chez l’être humain. Nous ne vendons pas aux patients.


Olaparib-d 4 -1
Cas No.: 2143107-55-3
10mM (in 1mL DMSO)In Stock
$792.00
1
1mgIn Stock
$238.00
1

Citations

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    Nature
    641, 529–536 (2025)
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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    35, 97–116 (2025)
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    34, 683–706 (2024)
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    31, 1291–1307 (2021)

Description

Olaparib -d 4 -1 (AZD2281-d 4 -1) is the deuterium labeled Olaparib. Olaparib is a potent and orally active PARP inhibitor with IC50 s of 5 and 1 nM for PARP1 and PARP2, respectively. Olaparib is an autophagy and mitophagy activator [1] [2] [3] [4].

In Vitro, Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.

References:
[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.
[2]. Menear KA, et al. 4-[3-(4-cyclopropanecarbonylpiperazine-1-carbonyl)-4-fluorobenzyl]-2H-phthalazin-1-one: a novel bioavailable inhibitor of poly(ADP-ribose) polymerase-1. J Med Chem. 2008 Oct 23;51(20):6581-91
[3]. Senra JM, et al. Inhibition of PARP-1 by olaparib (AZD2281) increases the radiosensitivity of a lung tumor xenograft.Mol Cancer Ther. 2011 Oct;10(10):1949-58.
[4]. Yasukawa M, et al. Synergetic Effects of PARP Inhibitor AZD2281 in Oral Squamous Cell Carcinoma in Vitro and in Vivo. Int J Mol Sci. 2016 Feb 24;17(3):272.
[5]. Bian X, et al. PTEN deficiency sensitizes endometrioid endometrial cancer to compound PARP-PI3K inhibition but not PARP inhibition as monotherapy. Oncogene. 2018 Jan 18;37(3):341-351.

Documents produit (Product Documents)

Purity:>98.50%Appearance:A solid

Propriétés chimiques (Chemical Properties)

N° CAS
2143107-55-3
Synonymes
AZD2281-d₄-1; KU0059436-d₄-1; MK-7339-d₄-1
Formule moléculaire
C24H19D4FN4O3
Masse moléculaire
438.49
Solubilité
DMSO: 100 mg/mL (228.06 mM; Need ultrasonic)
Conservation
Store at -20°C
Conditions d’expédition
Les échantillons d’évaluation sont expédiés avec des blocs réfrigérants. Les autres formats sont expédiés à température ambiante ou, sur demande, avec des blocs réfrigérants.

Calculateurs (Calculators)Molarité / Dilution / Masse moléculaire / Conversion d’unités / Formulation in vivo / Solubilité

g/mol

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