Nhận Dạng Quốc Tế & Đặc Tính Hóa Học
Monoisotopic mass
821.075438294
InChI
InChI=1S/C26H40Cl4N5O10PS.ClH/c27-7-11-34(12-8-28)46(42,35(13-9-29)14-10-30)45-15-16-47(43,44)18-22(33-23(36)6-5-21(31)26(40)41)24(37)32-17-19-3-1-2-4-20(19)25(38)39;/h1-4,21-22H,5-18,31H2,(H,32,37)(H,33,36)(H,38,39)(H,40,41);1H
InChI Key
InChIKey=KCMFHEVIGACFOM-UHFFFAOYSA-N
IUPAC Name
2-{[2-(4-amino-4-carboxybutanamido)-3-{[2-({bis[bis(2-chloroethyl)amino]phosphoryl}oxy)ethane]sulfonyl}propanamido]methyl}benzoic acid hydrochloride
Traditional IUPAC Name
2-{[2-(4-amino-4-carboxybutanamido)-3-[2-({bis[bis(2-chloroethyl)amino]phosphoryl}oxy)ethanesulfonyl]propanamido]methyl}benzoic acid hydrochloride
SMILES
Cl.NC(CCC(=O)NC(CS(=O)(=O)CCOP(=O)(N(CCCl)CCCl)N(CCCl)CCCl)C(=O)NCC1=CC=CC=C1C(O)=O)C(O)=O
pKa (strongest acidic)
1.4
pKa (Strongest Basic)
8.91
Refractivity
177.19 m3·mol-1
Cơ Chế Tác Dụng :
Canfosfamide is an active agent in chemotherapy-resistant ovarian cancer.
S-transferase P1-1 (GST P1-1) is an enzyme overexpressed in many human cancer cells. High levels of GST P1-1 are associated with a poor prognosis and resistance to certain chemotherapeutics. The activation of canfosfamide occurs when GST P1-1 splits canfosfamide into two active fragments: a glutathione analog fragment and an active cytotoxic fragment. The cytotoxic fragment reacts with important cell components, including RNA, DNA and proteins, leading to cell death. The glutathione analog fragment of canfosfamide may remain bound to GST P1-1, which may limit the ability of GST P1-1 to inactivate other cancer drugs.
Dược Động Học :
▧ Half Life :
18 min
Độc Tính :
Canfosfamide-related toxicities included grade 1-2 nausea, vomiting, fatigue, transient microscopic hematuria, and anemia.
Chỉ Định :
Intended for the treatment of various forms of cancer.