PF-07104091

PF-07104091 Suppliers list
Company Name: Chengdu PEIP Pharmaceutical Technology Co., LTD.  Gold
Tel: 028-61715638 18011352545
Email: 1242335275@qq.com
Company Name: Chembest Research Laboratories Limited  
Tel: 021-20908456
Email: sales@BioChemBest.com
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
Tel: 18149758185 18149758185
Email: sales-cpd@caerulumpharma.com
Company Name: Shanghai Lollane Biological Technology Co.,Ltd.  
Tel: 021-52996696,15000506266 15000506266
Email:
Company Name: Shanghai PharmaPartner Co., Ltd.  
Tel: 19983777532
Email: pharmabridge@163.com

PF-07104091 manufacturers

  • PF07104091
  • PF07104091 pictures
  • $131.00
  • 2026-07-31
  • CAS:2460249-19-6
  • Purity: 99.59%
  • Supply Ability: 10g
PF-07104091 Basic information
Uses
Product Name:PF-07104091
Synonyms:PF-07104091;(1R,3S)-3-[3-[[5-(methoxymethyl)-2-methyl-pyrazole-3-carbonyl]amino]-1H-pyrazol-5-yl]cyclopentyl] N-isopropylcarbamate;PF 7104091;PF7104091;PF-7104091;PF07104091, 10 mM in DMSO;(1R,3S)-3-(5-(3-(methoxymethyl)-1-methyl-1H-pyrazole-5-carboxamido)-1H-pyrazol-3-yl)cyclopentyl isopropylcarbamate;(1R,3S)-3-(3-(3-(methoxymethyl)-1-methyl-1H-pyrazole-5-carboxamido)-1H-pyrazol-5-yl)cyclopentyl isopropylcarbamate
CAS:2460249-19-6
MF:C19H28N6O4
MW:404.47
EINECS:
Product Categories:
Mol File:2460249-19-6.mol
PF-07104091 Structure
PF-07104091 Chemical Properties
Boiling point 567.0±50.0 °C(Predicted)
density 1.38±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO: Sparingly soluble: 1-10 mg/ml
Ethanol: Sparingly soluble: 1-10 mg/ml
pka12.51±0.46(Predicted)
InChIKeyMTNBRBDFNSGQKB-DCHPQEBHNA-N
SMILESN(C1NN=C([C@H]2CC[C@@H](OC(=O)NC(C)C)C2)C=1)C(C1N(N=C(COC)C=1)C)=O |&1:5,8,r|
Safety Information
MSDS Information
PF-07104091 Usage And Synthesis
UsesPF-07104091 can be used to treat advanced solid tumors, especially hormone receptor-positive (HR+)/HER2-negative breast cancer that is resistant to CDK4/6 inhibitors.
DescriptionPF-07104091 is an inhibitor of cyclin-dependent kinase 2 (Cdk2; Ki = 1.16 nM).1 It is selective for Cdk2 over glycogen synthase kinase 3β (GSK3β; Ki = 537.81 nM). PF-07104091 decreases proliferation of TOV-21G and OVCAR-3 ovarian and HCT116 colorectal cancer cells (IC50s = 4.8, 0.59, and 0.88 µM, respectively).2 In vivo, PF-07104091 (50 mg/kg per day) reduces tumor volume and weight in an HCT116 mouse xenograft model.WARNING This product is not for human or veterinary use.
References[1] JUN TANG . Anilinopyrazole as selective CDK2 inhibitors[J]. Bioorganic & Medicinal Chemistry Letters, 2003, 13 18: Pages 2985-2988. DOI: 10.1016/s0960-894x(03)00630-9
[2] LIU Z, YANG Y, SUN X, et al. Discovery of Novel Antitumor Small-Molecule Agent with Dual Action of CDK2/p-RB and MDM2/p53[J]. Molecules, 2024, 33 1. DOI: 10.3390/molecules29030725
PF-07104091 Preparation Products And Raw materials
Tag:PF-07104091(2460249-19-6) Related Product Information
PF-07104091 Carbamic acid, N-(1-methylethyl)-, (1R,3S)-3-[5-[[[3-(methoxymethyl)-1-methyl-1H-pyrazol-5-yl]carbonyl]amino]-1H-pyrazol-3-yl]cyclopentyl ester, hydrate (1:1) PF 477736 Dacomitinib (PF299804) PF-04691502 PF-04979064