5-Fluorouracil
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5-Fluorouracil
structure -
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CAS No:
51-21-8
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Formula:
C4H3FN2O2
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Chemical Name:
5-Fluorouracil
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Synonyms:
2,4(1H,3H)-Pyrimidinedione,5-fluoro-;Uracil,5-fluoro-;5-Fluoro-2,4(1H,3H)-pyrimidinedione;NSC 19893;Ro 2-9757;5-Fluorouracil;Fluorouracil;2,4-Dioxo-5-fluoropyrimidine;Efudex;5-FU;Fluracil;Fluril;Fluoroplex;5-Fluoro-2,4-pyrimidinedione;Fluoroblastin;Phtoruracil;Phthoruracil;Fluracilum;Efurix;Queroplex;Arumel;Kecimeton;Adrucil;Efudix;Carzonal;Ulup;Ftoruracil;U 8953;Timazin;FU;Fluri;5-Fluoracyl;Carac;2,4-Dihydroxy-5-fluoropyrimidine;Fluracedyl;5-Fluoropyrimidine-2,4-diol;Flurablastin;DBL;5-Fluoro-1H-pyrimidine-2,4-dione;Fluorouracile Accord;5-Oncouracil;Sigma 03738;5-Fluoro-2,4-dihydroxypyrimidine;1004-03-1;4921-97-5;79108-01-3
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CAS No:
Description
White or almost white, crystalline powder Fluorouracil is a white crystalline solid. Practically odorless.
Characteristics
58.2
-0.8
white powder
1.4593 (estimate)
282 °C (decomp)
190-200°C/0.1mmHg
196.5ºC
1.542
H2O: 12.2 g/L 20 ºC
Storeat0-5
2.68X10-6 mm Hg at 25 deg C (est)
LD50 orally in Rabbit: 230 mg/kg
PRACTICALLY ODORLESS
8.02None
Safety Information
Ⅲ
6.1
UN 2811 6.1/PG 3
3
22-20/21/22-52-25
36-36/37-36/37/39-22-45-26
YR0350000
Xn,T,C,Xi
Irritant/Highly Toxic
Stable. Light sensitive. Combustible. Incompatible with strong oxidizing agents, strong bases.
P201, P202, P260, P264, P270, P281, P301+P310, P308+P313, P314, P321, P330, P405, P501
H301
5-Fluorouracil Use and Manufacturing
5-Fluoro Uracil is an active metabolite of Doxifluridine(D556750).
Computed Properties
Molecular Weight:130.08
XLogP3:-0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Exact Mass:130.01785550
Monoisotopic Mass:130.01785550
Topological Polar Surface Area:58.2
Heavy Atom Count:9
Complexity:199
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
This product is first converted into 5-fluoro-2-deoxyuridine nucleotide in the body, which inhibits thymine nucleotide synthetase, blocking the conversion of deoxyuridine nucleotide into deoxythymine nucleotide, thereby inhibiting DNA biosynthesis. In addition, by preventing uracil and orotic acid from incorporating into RNA, the effect of inhibiting RNA synthesis is achieved. This product is a cell cycle-specific drug that mainly inhibits S-phase cells.
Registered Holders
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Nantong Jinghua Pharmaceutical Co Ltd
Active
United States
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IMCD Switzerland AG
Active
Switzerland
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TAPI NL B.V.
Active
France
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