1207456-01-6
- Product Name:Talazoparib
- Molecular Formula:C19H14F2N6O
- Purity:99%
- Molecular Weight:380.35
Product Details:
CasNo: 1207456-01-6
Molecular Formula: C19H14F2N6O
Appearance: White to off-white Powder
Packing: Aluminium bag
Throughput: 100KG/Month
Purity: 99%
Physical‑Chemical Properties
Appearance: White to yellow solid / powderDailyMed Sparingly soluble in water; soluble in DMSO and many organic solvents. Light‑sensitive.
Mechanism of Action
Talazoparib tosylate is a highly potent, orally‑bioavailable PARP‑1 and PARP‑2 inhibitor. It exerts dual‑mode anti‑tumour activity: catalytic inhibition of PARP enzyme plus strong PARP‑trapping effect. It locks PARP‑DNA complex at DNA‑strand‑break sites, blocks DNA damage‑repair process. Tumour cells with defective homologous‑recombination‑repair (such as BRCA1 / BRCA2 mutation) cannot repair accumulated DNA double‑strand breaks, leading to cancer‑cell apoptosis and synthetic lethalityEuropean M.... Among marketed PARP inhibitors, talazoparib exhibits outstanding PARP‑trapping potency.
Indications
- Monotherapy: For adult patients with germline BRCA‑mutated, HER2‑negative locally advanced or metastatic breast cancer (deleterious or suspected deleterious BRCA1/2 mutation)Pfizer Med....
- Combination therapy with enzalutamide: For adult patients with HRR‑gene‑mutated metastatic castration‑resistant prostate cancer (mCRPC)Pfizer Med....
Note: Patient selection should rely on approved companion diagnostic tests for BRCA or HRR gene alterations.
API Quality Profile
- HPLC Purity: NLT 98.0%
- Total impurities: ≤1.0%, single unknown impurity ≤0.15%
- Loss on drying: ≤0.5%
- COA, HPLC, NMR, MS available for R&D and formulation development. No official EP/USP pharmacopoeia monograph published yet.
Storage & Packing
Store in tightly‑closed container, protect from light, storage temperature ≤30 °C. Long‑term storage recommended at 2‑8 °C. Available packing: 1 g, 5 g, 10 g, 100 g, 1 kg aluminium foil bag / drum for lab‑scale and pilot manufacture.
Disclaimer
This product description serves for pharmaceutical raw‑material reference only, not for clinical medication guidance.
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