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Dacomitinib (PF299804)

CAS No.
1110813-31-4
Chemical Name:
Dacomitinib (PF299804)
Synonyms
Dacomitinib;PF299804;(E)-N-(4-((3-chloro-4-fluorophenyl)aMino)-7-Methoxyquinazolin-6-yl)-4-(piperidin-1-yl)but-2-enaMide;(2E)-N-[4-[(3-Chloro-4-fluorophenyl)amino]-7-methoxy-6-quinazolinyl]-4-(1-piperidinyl)-2-butenamide Dacomitinib (PF299804, PF299);PF299;CS-168;Dachtini;Dakotinib;dacatinib;PF-00299804
CBNumber:
CB22566418
Molecular Formula:
C24H25ClFN5O2
Molecular Weight:
469.94
MDL Number:
MFCD19443734
MOL File:
1110813-31-4.mol
Last updated:2023-12-27 14:48:58

Dacomitinib (PF299804) Properties

Melting point 184-187°C
Boiling point 665.7±55.0 °C(Predicted)
Density 1.344
storage temp. Refrigerator
solubility DMSO (Slightly), Methanol (Slightly, Heated)
form White solid.
pka 12.05±0.43(Predicted)
color White to Pale Yellow
CAS DataBase Reference 1110813-31-4
NCI Dictionary of Cancer Terms dacomitinib; PF-00299804
FDA UNII 2XJX250C20
NCI Drug Dictionary dacomitinib
ATC code L01EB07

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
HS Code  29335990

Dacomitinib (PF299804) price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical D5450 Dacomitinib >98.0%(HPLC) 1110813-31-4 50mg $145 2023-06-20 Buy
TCI Chemical D5450 Dacomitinib >98.0%(HPLC) 1110813-31-4 250mg $494 2023-06-20 Buy
Cayman Chemical 9001879 PF-299804 ≥98% 1110813-31-4 1mg $44 2024-03-01 Buy
Cayman Chemical 9001879 PF-299804 ≥98% 1110813-31-4 5mg $193 2024-03-01 Buy
Cayman Chemical 9001879 PF-299804 ≥98% 1110813-31-4 10mg $341 2024-03-01 Buy
Product number Packaging Price Buy
D5450 50mg $145 Buy
D5450 250mg $494 Buy
9001879 1mg $44 Buy
9001879 5mg $193 Buy
9001879 10mg $341 Buy

Dacomitinib (PF299804) Chemical Properties,Uses,Production

Description

Dacomitinib is a selective and irreversible inhibitor of EGFR. It is a drug candidate for the treatment of non-small cell lung carcinoma. It is current under the Phase III clinical trials. It also shows potential for the treatment of HER-2 amplified breast cancer cells lines that are resistant to trastuzumab and lapatinib. 

Biological activity

Dacomitibib (Dacomitinib, PF299804) is an effective and irreversible pan-ErbB inhibitor that is most effective in EGFR, with an IC50 of 6 nM. It is also highly effective in NSCLCs that carries EGFR or ERBB2 mutants (against Gefitinib) and EGFR T790M mutant. Phase 2.
Dacomitinib is taken orally once-daily. It is an irreversible inhibitor of HER-1 (EGFR), HER-2 and HER-4 tyrosine kinases. Dacomitinib targets multiple receptors of the HER pathway, whereas currently marketed HER-1 (EGFR) inhibitors for non-small cell lung cancer (NSCLC) target only one receptor in this pathway,developed by Pfizer.

Uses

Dacomitinib (PF299804), which name is (E)-N-[4-(3-chloro-4-fluoroanilino)-7- methoxyquinazolin-6-yl]-4-piperidin-1-ylbut-2-enamide, is a potent, orally available, highly selective, irreversible small-molecule tyrosine kinase inhibitor (TKI) of tyrosine kinase human epidermal growth factor receptors (HER) 1 (EGFR), HER2, and HER4. It is most effective against EGFR with IC50 of 6 nM. It is highly effective against NSCLCs carrying EGFR or ERBB2 mutant (anti-Gefitinib) and EGFR T790M mutant.

Clinical Study

Dacomitinib has advanced to several Phase III clinical trials. The results of the first trials were disappointing, with a failure to meet the study goals, Additional Phase III trials are ongoing.
Clinical evaluation of dacomitinib is ongoing in a number of clinical trials in patients with advanced NSCLC across lines of therapies and a range of histologies and molecular subtypes, such as EGFR and KRAS status.
Additionally, there is an ongoing clinical trial evaluating dacomitinib in recurrent and/or metastatic (RM) squamous cell carcinoma of the head and neck (SCCHN).

Description

The epidermal growth factor receptors (EGFR), whose members include ErbB1 (HER1), ErbB2 (HER2), ErbB3 (HER3), and ErbB4 (HER4), are receptor tyrosine kinases that are often over-expressed in cancer. PF-299804 is a second generation pan-ErbB receptor tyrosine kinase inhibitor (IC50s = 6, 45.7, and 73.7 nM for ErbB1, ErbB2, and ErbB4, respectively) that irreversibly binds to the ATP site in the catalytic domains of ErbB receptors. At 15 mg/kg, it demonstrates antitumor activity ranging from delay in tumor growth to complete regression in various tumor xenograft models expressing either wild-type ErbB or mutant ErbB family members that show resistance to first generation ErbB kinase inhibitors.

Uses

Dacomitinib is an Erb-inhibitor, or an inhibitor of the members of the epidermal growth factor receptor family. Used as an ant-cancer agent due to observation of over-expressed epidermal growth factor receptor in nearly all cases of squamous cell carcinoma in the head and neck.

Uses

PF299804 is a potent, irreversible pan-ErbB inhibitor against ErbB1, ErbB2 and ErbB4 with IC50 of 6 nM, 45.7 nM and 73.7 nM, respectively.

Definition

ChEBI: A member of the class of quinazolines that is 7-methoxyquinazoline-4,6-diamine in which the amino group at position 4 is substituted by a 3-chloro-4-fluorophenyl group and the amino group at position 6 is substituted by an (E)-4-(piperidin 1-yl)but-2-enoyl group.

in vitro

dacomitinib reduced the phosphorylation of her2, egfr, her4, akt, anderkin the majority of sensitive lines. dacomitinib exerted its antiproliferative effect through a combined g0–g1 arrest and an induction of apoptosis. dacomitinib inhibited growth in several her2-amplified lines with de novo and acquired resistance to trastuzumab. dacomitinib maintained a high activity in lines with acquired resistance to lapatinib. this study identifies her2-amplified breast cancer lines as most sensitive to the antiproliferative effect of dacomitinib and provides a strong rationale for its clinical testing in her2-amplified breast cancers resistant to trastuzumab and lapatinib [1].

in vivo

to evaluate the in vivo efficacy of pf00299804, the authors generated xenografts in nu/nu mice using hcc827 gfp and hcc827 del/t790m cells and treated the mice with pf00299804. pf00299804 effectively inhibited the growth of hcc827 gfp xenografts. pf00299804 treatment was substantially more effective at inhibiting growth of this xenograft model than gefinitib. thus, these preclinical models suggest that pf00299804 may be quite effective against lung cancers that become resistant to gefitinib or erlotinib via acquisition of a t790m mutation in egfr [2].

target

ErbB1

IC 50

6 nm (egfr); 45.7 nm (erbb2); 73.7 nm (erbb4)

storage

Store at +4°C

References

[1] kalous o, conklin d, desai aj, o'brien na, ginther c, anderson l, cohen dj, britten cd, taylor i, christensen jg, slamon dj, finn rs. dacomitinib (pf-00299804), an irreversible pan-her inhibitor, inhibits proliferation of her2-amplified breast cancer cell lines resistant to trastuzumab and lapatinib. mol cancer ther. 2012;11(9):1978-87.
[2] engelman ja, zejnullahu k, gale cm, lifshits e, gonzales aj, shimamura t, zhao f, vincent pw, naumov gn, bradner je, althaus iw, gandhi l, shapiro gi, nelson jm, heymach jv, meyerson m, wong kk, jfinne pa. pf00299804, an irreversible pan-erbb inhibitor, is effective in lung cancer models with egfr and erbb2 mutations that are resistant to gefitinib. cancer res. 2007;67(24):11924-32.

Dacomitinib (PF299804) Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 340)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Yanxi Chemical Co., Ltd.
+8617531190177 peter@yan-xi.com China 5993 58
shandong perfect biotechnology co.ltd
+86-53169958659; +8618596095638 sales@sdperfect.com China 294 58
Zibo Hangyu Biotechnology Development Co., Ltd
+86-0533-2185556 +8617865335152 Mandy@hangyubiotech.com China 11013 58
Anhui Ruihan Technology Co., Ltd
+8617756083858 daisy@anhuiruihan.com China 994 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Shanghai Bojing Chemical Co.,Ltd.
+86-86-02137122233 +8613795318958 bj1@bj-chem.com China 298 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9352 55
Nanjing Finetech Chemical Co., Ltd.
025-85710122 17714198479 sales@fine-chemtech.com CHINA 885 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58

Related articles

View Lastest Price from Dacomitinib (PF299804) manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Dacomitinib pictures 2024-03-12 Dacomitinib
1110813-31-4
US $0.00 / g 1g 98% HPLC 1kg shandong perfect biotechnology co.ltd
Dacomitinib (PF299804) pictures 2024-01-02 Dacomitinib (PF299804)
1110813-31-4
US $60.00-600.00 / kg 10kg 0.99 20tons Zibo Hangyu Biotechnology Development Co., Ltd
Dacomitinib pictures 2023-12-23 Dacomitinib
1110813-31-4
US $0.00-0.00 / kg 1kg 99%,single impurity<0.1 1 ton Nanjing Fred Technology Co., Ltd
  • Dacomitinib pictures
  • Dacomitinib
    1110813-31-4
  • US $0.00 / g
  • 98% HPLC
  • shandong perfect biotechnology co.ltd
  • Dacomitinib pictures
  • Dacomitinib
    1110813-31-4
  • US $0.00-0.00 / kg
  • 99%,single impurity<0.1
  • Nanjing Fred Technology Co., Ltd

Dacomitinib (PF299804) Spectrum

PF-00299804-03 PF-00299804 DacoMitinib (PF-00299804) DacoMitinib,PF299804 DacoMitinib (PF299804,PF-00299804) PF299804;DACOMITINIB DacoMitinib (PF299804, PF299) (E)-N-(4-((3-chloro-4-fluorophenyl)aMino)-7-Methoxyquizolin-6-yl)-4-(piperidin-1-yl)but-2-eMide dacomitinib (pan-HER inhibitor) (E)-N-[4-(3-chloro-4-fluoroanilino)-7-methoxyquinazolin-6-yl]-4-piperidin-1-ylbut-2-enamide Dacomitinib, >=98% 2-Butenamide,N-[4-[(3-chloro-4-fluorophenyl)amino]-7-methoxy-6-quinazolinyl]-4-(1-piperidinyl)-, (2E)- PF299 PF299804;(E)-N-(4-((3-CHLORO-4-FLUOROPHENYL)AMINO)-7-METHOXYQUINAZOLIN-6-YL)-4-(PIPERIDIN-1-YL)BUT-2-ENAMIDE (2E)-N-[4-[(3-Chloro-4-fluorophenyl)amino]-7-methoxy-6-quinazolinyl]-4-(1-piperidinyl)-2-butenamide PF299804 (Dacomitinib, PF299) PF299804, PF299) PF-299804 (Dacomitinib,PF-00299804) CS-168 PF299804; DACOMITINIB; PF-00299804;PF-299804;PF 299804 Dacomitinib, 98%, a potent irreversible ErbB inbibitor Dacomitinib (USAN/INN) Dacomitinib [USAN] Dacomitinib Dacomitinib Dacomitinib-D10 Dacomitinib (PF299804) USP/EP/BP Dacomitinib dihydrochloride salt Dacomitinib D10 dihydrochlorideQ: What is Dacomitinib D10 dihydrochloride Q: What is the CAS Number of Dacomitinib D10 dihydrochloride Dacomitinib D3 Dacomitinib D5 Dacomitinib (2E)-N-[4-[(3-Chloro-4-fluorophenyl)amino]-7-methoxy-6-quinazolinyl]-4-(1-piperidinyl)-2-butenamide Dacomitinib (PF299804, PF299) PF299804 (E)-N-(4-((3-chloro-4-fluorophenyl)aMino)-7-Methoxyquinazolin-6-yl)-4-(piperidin-1-yl)but-2-enaMide Dachtini Dacomitinib free base Dacomitinib / PF 00299804-03 Dakotinib dacatinib 1110813-31-4 C24H25ClFN5O2 Inhibitors Anti-cancer&immunity API API 1 APIs