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Home CSSS06744480053

Structure Info


Chemspace ID
CSSS06744480053 (In-Stock Screening Compounds)
MFCD
MFCD09873271
IUPAC Name
7-{[3-({4-[(3-chloro-4-fluorophenyl)amino]-6-methoxyquinazolin-7-yl}oxy)propyl]amino}-N,N-dimethyl-2,1,3-benzoxadiazole-4-sulfonamide
Mol formula
C26H25ClFN7O5S
Mol weight
602 Da
Catalog Number(s)
AG02DHZU, BN88882, HY-152098, T75015

Properties

LogP
3.63
Heavy atoms count
41
Rotatable bond count
10
Number of rings
5
Carbon bond saturation, Fsp3
0.23
Polar surface area (Å)
145
Hydrogen bond acceptors count
10
Hydrogen bond donors count
2

SDS

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Items Overall 8 items from 2 suppliers

SupplierLead timeShips fromPurityPackPrice, €Qty
MedChemExpress10 daysUnited States
To:
995 mg368
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MedChemExpress10 daysUnited States
To:
9910 mg588
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MedChemExpress10 daysUnited States
To:
9925 mg1,176
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MedChemExpress10 daysUnited States
To:
9950 mg1,863
Go to cartEnquire
Description: Names: HX103; Product Description: HX103 is an epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI)-based fluorogenic probe. HX103 inhibits EGFR 19 del , EGFR L858R , EGFR wild type and EGFR T790M with IC 50 s of 1.3, 1.5, 4.0 and 977 nM, respectively. HX103 can be used for quantifying active-EGFR to predict agent sensitivity in NSCLC patients with EGFR-activating mutations .; Target: EGFR; CAS: 2566466-98-4
MedChemExpress EU10 daysSweden
To:
995 mg387
Go to cartEnquire
MedChemExpress EU10 daysSweden
To:
9910 mg620
Go to cartEnquire
MedChemExpress EU10 daysSweden
To:
9925 mg1,240
Go to cartEnquire
MedChemExpress EU10 daysSweden
To:
9950 mg1,963
Go to cartEnquire
Description: Names: HX103; Product Description: HX103 is an epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI)-based fluorogenic probe. HX103 inhibits EGFR 19 del, EGFR L858R, EGFR wild type and EGFR T790M with IC50s of 1.3, 1.5, 4.0 and 977 nM, respectively. HX103 can be used for quantifying active-EGFR to predict agent sensitivity in NSCLC patients with EGFR-activating mutations; Target: EGFR; CAS: 2566466-98-4
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