Tenalisib

Tenalisib Suppliers list
Company Name: MedChemexpress LLC  
Tel: 021-58955995
Email: sales@medchemexpress.cn
Company Name: Zhengzhou HSH Science & Technology Co., Ltd.  
Tel: 0371-55932928 18937192232;
Email: 1282296214@qq.com
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
Tel: 18149758185 18149758185
Email: sales-cpd@caerulumpharma.com
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com
Company Name: Sichuan Wei Keqi Biological Technology Co., Ltd.  
Tel: 028-81700200 18116577057
Email: 3003855609@qq.com

Tenalisib manufacturers

  • Tenalisib
  • Tenalisib pictures
  • $38.00
  • 2026-07-27
  • CAS:1639417-53-0
  • Purity: 99.71%
  • Supply Ability: 10g
  • Tenalisib
  • Tenalisib pictures
  • $38.00
  • 2026-07-27
  • CAS:1639417-53-0
  • Purity: 99.71%
  • Supply Ability: 10g
Tenalisib Basic information
Product Name:Tenalisib
Synonyms:RP6530;Tenalisib;Tenalisib (RP6530);RP6530, Tenalisib;Tenalisib (Synonyms: RP6530);RP-6530; RP 6530; RP6530;4H-1-Benzopyran-4-one, 3-(3-fluorophenyl)-2-[(1S)-1-(9H-purin-6-ylamino)propyl]-;(S)-2-(1-((9H-Purin-6-yl)amino)propyl)-3-(3-fluorophenyl)-4H-chromen-4-one
CAS:1639417-53-0
MF:C23H18FN5O2
MW:415.42
EINECS:
Product Categories:
Mol File:1639417-53-0.mol
Tenalisib Structure
Tenalisib Chemical Properties
Boiling point 706.1±60.0 °C(Predicted)
density 1.434±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : ≥ 100 mg/mL (240.72 mM)
form Solid
pka10.06±0.10(Predicted)
color White to off-white
Safety Information
MSDS Information
Tenalisib Usage And Synthesis
UsesTenalisib (RP6530) is a novel, potent, and selective PI3Kδ and PI3Kγ inhibitor with IC50 values of 25 and 33 nM, respectively.
in vivo

Tenalisib has been well tolerated in subjects with heavily pre-treated relapsed/refractory hematologic malignancies. Reported toxicities are manageable with no DLTs. Single agent activity is evident in difficult-to-treat subjects at ≥ 200 mg BID[2].

IC 50PI3Kδ: 25 nM (IC50); PI3Kγ: 33 nM (IC50)
References[1] Vakkalanka S, et al. RP6530, a dual PI3K δ/γ inhibitor, potentiates ruxolitinib activity in the JAK2-V617F mutant erythroleukemia cell lines. [abstract]. In: Proceedings of the 106th Annual Meeting of the American Association for Cancer Research; 2015 Apr 18-22; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2015;75(15 Suppl):Abstract nr 2704. doi:10.1158/1538-7445.AM2015-2704
[2] Carmelo C, et al. A Dose Escalation Study of RP6530, a Novel Dual PI3K Delta/Gamma Inhibitor, in Patients with Relapsed/Refractory Hematologic Malignancies. Blood 2015 126:1495;
Tenalisib Preparation Products And Raw materials
Tag:Tenalisib(1639417-53-0) Related Product Information
S14161 PF-04691502 LY3023414 NVP-BGT226 HS-173 NVP-BEZ 235