Warning!
Your browser does not support HTML5.
Display of the content may be incorrect. Please make sure that your browser supports HTML5 syntax.
Search for Small Molecules by SMILES, name, CAS, MFCD, ID, InChI Key
Search for Biologics by ID, Target name, CAS, Protein name, Gene ID, Clone ID, Source Organism
0
0.00 $
Currency
Home CSSS00000051173

Structure Info

Chemspace ID
CSSS00000051173 (In-Stock Screening Compounds)
CAS
184475-35-2
MFCD
MFCD04307832
IUPAC Name
N-(3-chloro-4-fluorophenyl)-7-methoxy-6-[3-(morpholin-4-yl)propoxy]quinazolin-4-amine
Mol formula
C22H24ClFN4O3
Mol weight
447 Da
Catalog Number(s)
10496, 13166, 21432, 101029, 306578, 34a_100015190902_100000748698, 37923, A109874, A8219, AA0039I6, AB52186, ACM184475352, ACM184475352-2, ACS-524, ADB92939001, AG0039KY, AJ52186, AOS0039KY, APB184475352, AR003A9Y, ArZ-UP080933, ArZ-UP480321, B0084-306578, BB4LS-EN300-123024, BBF-04570, BD131918, BG164498, BISN0101, CB14314, CD31002885, CFN90011, CSC000051173, CT1946, DZB66449, EN300-123024, F079438, F231003, FG10816, G0546, G304000, H018, HY-50895, J10250, J94474, KS-1204, LAN-B42345, LN00175798, LQT-B42422, M12848, OSSL_882918, R633575, S1025, SAB-025327, SC-18023, SM00066, STK621310, SY002154, SYN1042, T1181, YBD160510, Z1546610485, Z1551429741, ZX-AE020634, ZX-CY002097, scs-524

Properties

LogP
3.75
Heavy atoms count
31
Rotatable bond count
8
Number of rings
4
Carbon bond saturation, Fsp3
0.363
Polar surface area (Å)
69
Hydrogen bond acceptors count
7
Hydrogen bond donors count
1

SDS

Choose Language:

If you wish to request SDS before ordering, please contact us at [email protected]

C22H24ClFN4O3
Zoom the structure
CSSS00000051173
 

Items Overall 36 items from 8 suppliers

SupplierLead timeShips fromPurityPackPrice, $Qty
Enamine Ltd5 daysUkraine
To:
901 mg83
Go to cartEnquire
Enamine Ltd5 daysUkraine
To:
902 mg85
Go to cartEnquire
Enamine Ltd5 daysUkraine
To:
905 mg91
Go to cartEnquire
Enamine Ltd5 daysUkraine
To:
9010 mg102
Go to cartEnquire
Enamine Ltd5 daysUkraine
To:
9020 mg123
Go to cartEnquire
MedChemExpress10 daysUnited States
To:
99100 mg60
Go to cartEnquire
MedChemExpress10 daysUnited States
To:
99500 mg72
Go to cartEnquire
MedChemExpress10 daysUnited States
To:
991 g90
Go to cartEnquire
MedChemExpress10 daysUnited States
To:
995 g180
Go to cartEnquire
MedChemExpress10 daysUnited States
To:
9910mM/1mL66
Go to cartEnquire
Description: Names: Gefitinib; ZD1839; Product Description: Gefitinib (ZD1839) is a potent, selective and orally active EGFR tyrosine kinase inhibitor with an IC 50 of 33 nM. Gefitinib selectively inhibits EGF-stimulated tumor cell growth (IC 50 of 54 nM) and that blocks EGF-stimulated EGFR autophosphorylation in tumor cells. Gefitinib also induces autophagy and cell apoptosis , which can be used for cancer related research, such as Lung cancer and breast cancer .; Target: Apoptosis;Autophagy;EGFR; CAS: 184475-35-2
Apexbio Technology LLC10 daysUnited States
To:
99100 mg67
Go to cartEnquire
Apexbio Technology LLC10 daysUnited States
To:
99250 mg77
Go to cartEnquire
Apexbio Technology LLC10 daysUnited States
To:
9910mM (in 1mL DMSO)61
Go to cartEnquire
Description: Name: Gefitinib (ZD1839); Selective EGFR inhibitor; Format: a solid; CAS: 184475-35-2
Key Organics Limited (BIONET)10 daysUnited Kingdom
To:
971 mg61
Go to cartEnquire
Key Organics Limited (BIONET)10 daysUnited Kingdom
To:
975 mg92
Go to cartEnquire
Key Organics Limited (BIONET)10 daysUnited Kingdom
To:
9710 mg128
Go to cartEnquire
MedChemExpress EU10 daysSweden
To:
99100 mg63
Go to cartEnquire
MedChemExpress EU10 daysSweden
To:
99500 mg75
Go to cartEnquire
MedChemExpress EU10 daysSweden
To:
991 g95
Go to cartEnquire
MedChemExpress EU10 daysSweden
To:
995 g190
Go to cartEnquire
MedChemExpress EU10 daysSweden
To:
9910mM/1mL69
Go to cartEnquire
Description: Names: Gefitinib; ZD1839; Product Description: Gefitinib (ZD1839) is a potent, selective and orally active EGFR tyrosine kinase inhibitor with an IC50 of 33 nM. Gefitinib selectively inhibits EGF-stimulated tumor cell growth (IC50 of 54 nM) and that blocks EGF-stimulated EGFR autophosphorylation in tumor cells. Gefitinib also induces autophagy and cell apoptosis, which can be used for cancer related research, such as Lung cancer and breast cancer ; Target: Apoptosis;Autophagy;EGFR; CAS: 184475-35-2
Princeton Biomolecular Research10 daysUnited States
To:
901 mg88
Go to cartEnquire
Princeton Biomolecular Research10 daysUnited States
To:
902 mg94
Go to cartEnquire
Princeton Biomolecular Research10 daysUnited States
To:
905 mg99
Go to cartEnquire
Princeton Biomolecular Research10 daysUnited States
To:
9010 mg116
Go to cartEnquire
Princeton Biomolecular Research10 daysUnited States
To:
9015 mg132
Go to cartEnquire
Princeton Biomolecular Research10 daysUnited States
To:
9020 mg143
Go to cartEnquire
Princeton Biomolecular Research10 daysUnited States
To:
9050 mg231
Go to cartEnquire
Princeton Biomolecular Research10 daysUnited States
To:
90100 mg297
Go to cartEnquire
Princeton Biomolecular Research10 daysUnited States
To:
903 umol94
Go to cartEnquire
Princeton Biomolecular Research10 daysUnited States
To:
905 umol99
Go to cartEnquire
ChemFaces12 daysChina
To:
901 mg6
Go to cartEnquire
Description: CAS: 184475-35-2
Targetmol Chemicals Inc30 daysUnited States
To:
99100 mg50
Go to cartEnquire
Targetmol Chemicals Inc30 daysUnited States
To:
99500 mg57
Go to cartEnquire
Targetmol Chemicals Inc30 daysUnited States
To:
991 g74
Go to cartEnquire
Targetmol Chemicals Inc30 daysUnited States
To:
995 g148
Go to cartEnquire
Description: Gefitinib (ZD1839) is an EGFR first-generation inhibitor with oral activity that inhibits the EGFR 19 Del and L858R mutations. Gefitinib has antitumor activity and is used for the treatment of EGFR-mutated non-small-cell lung cancers. Gefitinib administration RESULTS in the development of the EGFR C797S resistance mutation.; CAS: 184475-35-2
For a custom pack size or bulk
please drop us a line:Enquire