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PD 166866

CAS No.
192705-79-6
Chemical Name:
PD 166866
Synonyms
CS-2496;PD 166866;PD-166866;PD 166866;PD-166866, 10 mM in DMSO;FGF Receptor Tyrosine Kinase Inhibitor;FGF Receptor Tyrosine Kinase Inhibitor - CAS 192705-79-6 - Calbiochem;tert-butyl (2-amino-6-(3,5-dimethoxyphenyl)pyrido[2,3-d]pyrimidin-7-yl)carbamate;1-(2-aMino-6-(3,5-diMethoxyphenyl)pyrido[2,3-d]pyriMidin-7-yl)-3-(tert-butyl)urea;N-[2-AMino-6-(3,5-diMethoxyphenyl)pyrido[2,3-d]pyriMidin-7-yl]-N'-(1,1-diMethylethyl);Inhibitor,Autophagy,FGFR,inhibit,PD-166866,PD 166866,Fibroblast growth factor receptor
CBNumber:
CB42485694
Molecular Formula:
C20H24N6O3
Molecular Weight:
396.44
MDL Number:
MFCD12922514
MOL File:
192705-79-6.mol
MSDS File:
SDS
Last updated:2026-01-13 11:21:10
Product description Number Pack Size Price
PD-166866 ≥98% (HPLC) PZ0114 5mg $134
FGF Receptor Tyrosine Kinase Inhibitor 341608 5mg $201
PD 166866 ≥98% 22464 1mg $32
PD 166866 ≥98% 22464 5mg $93
PD-166866 ≥98% (HPLC) PZ0114 25mg $749
More product size

PD 166866 Properties

Melting point 291-293°C
storage temp. 2-8°C
solubility DMSO: ≥10mg/mL
form Off-white solid
color off-white to light tan
InChI 1S/C20H24N6O3/c1-20(2,3)26-19(27)25-17-15(8-12-10-22-18(21)24-16(12)23-17)11-6-13(28-4)9-14(7-11)29-5/h6-10H,1-5H3,(H4,21,22,23,24,25,26,27)
InChIKey NHJSWORVNIOXIT-UHFFFAOYSA-N
SMILES COc1cc(OC)cc(c1)-c2cc3cnc(N)nc3nc2NC(=O)NC(C)(C)C
FDA UNII NA856793UT
UNSPSC Code 51111800
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Hazard Codes  Xn
Risk Statements  22
WGK Germany  1
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

PD 166866 price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PZ0114 PD-166866 ≥98% (HPLC) 192705-79-6 5mg $134 2025-07-31 Buy
Sigma-Aldrich 341608 FGF Receptor Tyrosine Kinase Inhibitor 192705-79-6 5mg $201 2025-07-31 Buy
Cayman Chemical 22464 PD 166866 ≥98% 192705-79-6 1mg $32 2024-03-01 Buy
Cayman Chemical 22464 PD 166866 ≥98% 192705-79-6 5mg $93 2024-03-01 Buy
Sigma-Aldrich PZ0114 PD-166866 ≥98% (HPLC) 192705-79-6 25mg $749 2025-07-31 Buy
Product number Packaging Price Buy
PZ0114 5mg $134 Buy
341608 5mg $201 Buy
22464 1mg $32 Buy
22464 5mg $93 Buy
PZ0114 25mg $749 Buy

PD 166866 Chemical Properties,Uses,Production

Description

PD 166866 is a potent inhibitor of fibroblast growth factor receptor 1 (FGFR1; IC50 = 52.4 nM; Ki = 45.2 nM). It is selective for FGFR1 over PDGFR, EGFR, C-SRC, MEK, PKC, insulin receptor tyrosine kinase, and CDK4 (IC50s = >50 μM). PD 166866 inhibits FGFR1 autophosphorylation in NIH3T3 and L6 cells (IC50s = 10.8 and 3.1 nM, respectively) and inhibits phosphorylation of MAPK (IC50s = 4.3 and 7.9 nM for the 44- and 42-kDa MAPK isoforms, respectively). It reduces FGF- but not EGF- or PDGF-stimulated growth of L6 cells and inhibits microvessel outgrowth from human placental arteries in vitro. PD 166866 inhibits the growth of non-small cell lung cancer (NSCLC) cell lines in a dose-dependent manner and reduces migration of VL-8 cells at a concentration of 10 μM.

Chemical Properties

Off-White Solid

Uses

A novel potent ATP competitive pyrido[2,3-d]pyrimidine tyrosine kinase inhibitors. An inhibitor of the basic fibroplast growth factor (bFGF).

Definition

ChEBI: PD-166866 is a member of the class of pyridopyrimidines that is pyrido[2,3-d]pyrimidine substituted by an amino group at position 2, 3,5-dimethoxyphenyl group at position 6, and by a (tert-butylcarbamoyl)nitrilo group at position 7. It is a selective ATP competitive inhibitor of the human fibroblast growth factor-1 receptor (FGFR1) tyrosine kinase with an IC50 of 52.4 nM. It has a role as an apoptosis inducer, an antineoplastic agent, an EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor and an angiogenesis inhibitor. It is a dimethoxybenzene, a pyridopyrimidine, a member of ureas, a biaryl and a primary arylamine.

Biochem/physiol Actions

PD-166866 is a selective inhibitor of the FGF-1 receptor tyrosine kinase (FGFR1) with IC50 = 55 nM, and no effect on c-Src, PDGFR-b, EGFR or insulin receptor tyrosine kinases or MEK, PKC, and CDK4.

References

[1] R L PANEK. In vitro biological characterization and antiangiogenic effects of PD 166866, a selective inhibitor of the FGF-1 receptor tyrosine kinase.[J]. Journal of Pharmacology and Experimental Therapeutics, 1998, 286 1: 569-577.
[2] HENDRIK FISCHER. Fibroblast growth factor receptor-mediated signals contribute to the malignant phenotype of non-small cell lung cancer cells: therapeutic implications and synergism with epidermal growth factor receptor inhibition.[J]. Molecular Cancer Therapeutics, 2008, 7 10: 3408-3419. DOI: 10.1158/1535-7163.mct-08-0444

PD 166866 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 96)Suppliers
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ATK CHEMICAL COMPANY LIMITED
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Zibo Hangyu Biotechnology Development Co., Ltd
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View Lastest Price from PD 166866 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
PD 166866 pictures 2019-12-23 PD 166866
192705-79-6
US $1.00 / g 1g 99.99% 200kg Career Henan Chemical Co
  • PD 166866 pictures
  • PD 166866
    192705-79-6
  • US $1.00 / g
  • 99.99%
  • Career Henan Chemical Co

PD 166866 Spectrum

PD 166866 N-[2-AMino-6-(3,5-diMethoxyphenyl)pyrido[2,3-d]pyriMidin-7-yl]-N'-(1,1-diMethylethyl) 1-(2-aMino-6-(3,5-diMethoxyphenyl)pyrido[2,3-d]pyriMidin-7-yl)-3-(tert-butyl)urea tert-butyl (2-amino-6-(3,5-dimethoxyphenyl)pyrido[2,3-d]pyrimidin-7-yl)carbamate FGF Receptor Tyrosine Kinase Inhibitor CS-2496 FGF Receptor Tyrosine Kinase Inhibitor - CAS 192705-79-6 - Calbiochem PD-166866;PD 166866 Urea, N-[2-amino-6-(3,5-dimethoxyphenyl)pyrido[2,3-d]pyrimidin-7-yl]-N'-(1,1-dimethylethyl)- Inhibitor,Autophagy,FGFR,inhibit,PD-166866,PD 166866,Fibroblast growth factor receptor PD-166866, 10 mM in DMSO 1-[2-amino-6-(3,5-dimethoxyphenyl)pyrido[2,3-d]pyrimidin-7-yl]-3-tert-butylurea - [AC80747] 192705-79-6 API Amines Aromatics Bases & Related Reagents Heterocycles Intermediates & Fine Chemicals Nucleotides Pharmaceuticals