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经验公式(希尔记法):
C15H22FN3O6
化学文摘社编号:
分子量:
359.35
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
产品名称
卡培他滨, ≥98% (HPLC)
Quality Segment
assay
≥98% (HPLC)
form
powder
optical activity
[α]/D +80 to +100°, c = 0.5 in methanol
color
white to beige
solubility
H2O: 10 mg/mL, clear (warmed)
storage temp.
2-8°C
SMILES string
O[C@H]1[C@@H](O)[C@H](N2C(N=C(NC(OCCCCC)=O)C(F)=C2)=O)O[C@@H]1C
InChI
1S/C15H22FN3O6/c1-3-4-5-6-24-15(23)18-12-9(16)7-19(14(22)17-12)13-11(21)10(20)8(2)25-13/h7-8,10-11,13,20-21H,3-6H2,1-2H3,(H,17,18,22,23)/t8-,10-,11-,13-/m1/s1
InChI key
GAGWJHPBXLXJQN-UORFTKCHSA-N
Gene Information
human ... TYMS(7298)
Application
Capecitabine has been used:
- in combination with gemcitabine to achieve glutamine deprivation by enhancing the sensitivity of expression in pancreatic ductal adenocarcinoma (PDAC) cells to inhibitors of glutamine metabolism and study its effect on PDAC cell survival
- to study the drug metabolic function in a two-organ microfluidic system
- as an anti-cancer agent to study its cytotoxic activity alone or in combination with B87 on cancer cells
Biochem/physiol Actions
卡培他滨是一种抗癌药物,是去氧氟尿苷的前药,在肿瘤部位代谢为5-氟尿嘧啶。
卡培他滨是一种抗癌药物,是去氧氟尿苷的前药,在肿瘤部位代谢为5-氟尿嘧啶。 卡培他滨的激活遵循具有三个酶促步骤和两个中间代谢物5′-脱氧-5-氟胞苷(5′-DFCR)和5′-脱氧-5-氟尿苷(5′-DFUR)的途径,形成5-氟尿嘧啶。
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signalword
Danger
hcodes
Hazard Classifications
Carc. 1B - Muta. 2 - Repr. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
