Furagin

Modify Date: 2024-01-09 01:27:12

Furagin Structure
Furagin structure
Common Name Furagin
CAS Number 1672-88-4 Molecular Weight 264.194
Density 1.6±0.1 g/cm3 Boiling Point N/A
Molecular Formula C10H8N4O5 Melting Point 267-270ºC (dec.)
MSDS N/A Flash Point N/A

 Use of Furagin


Furagin, nitrofurantoin analog, is an anti-bacterial agent. Furagin is 2-substituted 5-nitrofuran, chemically and structurally similar to well-known antibacterial compound nitrofurantoin.IC50 Value: Target: Antibacterialin vitro: The furagin concentrations in serum remain several hours above the MIC concentrations of many pathogenic bacteria. Despite the high concentrations in serum, the urine levels of furagin were generally lower than those of nitrofurantoin. The 24 hr recoveries in urine were 8--13% for furagin and about 36% for nitrofurantoin [1].in vivo: A time-independent increase in SCE frequency was found in lymphocytes of children treated with furagin. Total CA frequency did not differ significantly between groups of children with various duration of furagin treatment [2]. Women were randomised into two groups receiving either ciprofloxacin 250mg twice a day for 3 days (n=13) or furagin 100mg three times a day for 7 days (n=14). Median lengths of follow-up were 4 days and 5 days in the ciprofloxacin and furagin groups, respectively [3].

 Names

Name 1-[(E)-[(E)-3-(5-nitrofuran-2-yl)prop-2-enylidene]amino]imidazolidine-2,4-dione
Synonym More Synonyms

 Furagin Biological Activity

Description Furagin, nitrofurantoin analog, is an anti-bacterial agent. Furagin is 2-substituted 5-nitrofuran, chemically and structurally similar to well-known antibacterial compound nitrofurantoin.IC50 Value: Target: Antibacterialin vitro: The furagin concentrations in serum remain several hours above the MIC concentrations of many pathogenic bacteria. Despite the high concentrations in serum, the urine levels of furagin were generally lower than those of nitrofurantoin. The 24 hr recoveries in urine were 8--13% for furagin and about 36% for nitrofurantoin [1].in vivo: A time-independent increase in SCE frequency was found in lymphocytes of children treated with furagin. Total CA frequency did not differ significantly between groups of children with various duration of furagin treatment [2]. Women were randomised into two groups receiving either ciprofloxacin 250mg twice a day for 3 days (n=13) or furagin 100mg three times a day for 7 days (n=14). Median lengths of follow-up were 4 days and 5 days in the ciprofloxacin and furagin groups, respectively [3].
Related Catalog
References

[1]. Mannisto P, et al. Pharmacokinetics of furagin, a new nitrofurantoin congener, on human volunteers. Int J Clin Pharmacol Biopharm. 1979 Jun;17(6):264-70.

[2]. Slapsyte G, et al. Cytogenetic analysis of children under long-term antibacterial therapy with nitroheterocyclic compound furagin. Mutat Res. 2001 Apr 5;491(1-2):25-30.

[3]. Dybowski B, et al. Ciprofloxacin and furagin in acute cystitis: comparison of early immune and microbiological results. Int J Antimicrob Agents. 2008 Feb;31(2):130-4.

 Chemical & Physical Properties

Density 1.6±0.1 g/cm3
Melting Point 267-270ºC (dec.)
Molecular Formula C10H8N4O5
Molecular Weight 264.194
Exact Mass 264.049469
PSA 120.73000
LogP 0.81
Index of Refraction 1.689
Storage condition Refrigerator

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
MU3870000
CHEMICAL NAME :
Hydantoin, 1-((3-(5-nitro-2-furyl)allylidene)amino)-
CAS REGISTRY NUMBER :
1672-88-4
BEILSTEIN REFERENCE NO. :
0307076
LAST UPDATED :
199612
DATA ITEMS CITED :
4
MOLECULAR FORMULA :
C10-H8-N4-O5
MOLECULAR WEIGHT :
264.22
WISWESSER LINE NOTATION :
T5OJ BNW E1U2UN- AT5NVMV EHJ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Phage inhibition capacity
TEST SYSTEM :
Bacteria - Escherichia coli
DOSE/DURATION :
3 mg/L
REFERENCE :
CJMIAZ Canadian Journal of Microbiology. (National Research Council of Canada, Publication Sales and Distribution, Ottawa ON K1A OR6, Canada) V.1- 1954- Volume(issue)/page/year: 10,932,1964

 Safety Information

HS Code 2934999090

 Synthetic Route

~%

Furagin Structure

Furagin

CAS#:1672-88-4

Literature: Yakugaku Zasshi, , vol. 75, p. 117,119, 120 Chem.Abstr., , p. 1782

 Precursor & DownStream

Precursor  2

DownStream  0

 Customs

HS Code 2934999090
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Synonyms

1-((3-(5-Nitro-2-furyl)allylidene)amino)-hydantoin
Furagin
MFCD00431319
1-{[(1E,2E)-3-(5-Nitro-2-furyl)prop-2-en-1-ylidene]amino}imidazolidine-2,4-dione
1-{(E)-[(2E)-3-(5-Nitro-2-furyl)-2-propen-1-ylidene]amino}-2,4-imidazolidinedione
1-[3-(5-Nitro-[2]furyl)-allylidenamino]-imidazolidin-2,4-dion
Furazidin
2,4-Imidazolidinedione, 1-[[(1E,2E)-3-(5-nitro-2-furanyl)-2-propen-1-ylidene]amino]-
Akritoin
Furazidine
1-[3-(5-nitro-[2]furyl)-allylidenamino]-imidazolidine-2,4-dione
NF 416
1-((3-(5-Nitrofuran-2-yl)allylidene)amino)imidazolidine-2,4-dione
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