Sinefungin

Modify Date: 2024-01-04 10:40:14

Sinefungin Structure
Sinefungin structure
 Common Name Sinefungin
CAS Number 58944-73-3 Molecular Weight 381.39
Density 1.9±0.1 g/cm3 Boiling Point 783.2±70.0 °C at 760 mmHg
Molecular Formula C15H23N7O5 Melting Point N/A
MSDS Chinese USA Flash Point 427.5±35.7 °C
Symbol GHS07
GHS07		 Signal Word Warning

 Use of Sinefungin


Sinefungin is a potent inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2'-)-methyltransferase, and viral multiplication[1]. Sinefungin, a SET7/9 inhibitor, ameliorates renal fibrosis by inhibiting H3K4 methylation [2].

 Names

Name sinefungin
Synonym More Synonyms

 Sinefungin Biological Activity

Description Sinefungin is a potent inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2'-)-methyltransferase, and viral multiplication[1]. Sinefungin, a SET7/9 inhibitor, ameliorates renal fibrosis by inhibiting H3K4 methylation [2].
Related Catalog
References

[1]. Pugh CS, et al. Sinefungin, a potent inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2'-)-methyltransferase, and viral multiplication. J Biol Chem. 1978 Jun 25;253(12):4075-7.

[2]. Sasaki K, et al. Inhibition of SET Domain-Containing Lysine Methyltransferase 7/9 Ameliorates Renal Fibrosis. J Am Soc Nephrol. 2016 Jan;27(1):203-15.

 Chemical & Physical Properties

Density 1.9±0.1 g/cm3
Boiling Point 783.2±70.0 °C at 760 mmHg
Molecular Formula C15H23N7O5
Molecular Weight 381.39
Flash Point 427.5±35.7 °C
Exact Mass 381.176056
PSA 208.65000
LogP -1.33
Vapour Pressure 0.0±2.8 mmHg at 25°C
Index of Refraction 1.832

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
HE3140000
CHEMICAL NAME :
D-glycero-alpha-L-talo-Decofuranuronic acid, 6,9-diamino-1-(6-amino-9H-purin-9-yl)- 1,5,6,7,8,9-hexadeoxy-
CAS REGISTRY NUMBER :
58944-73-3
LAST UPDATED :
199612
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C15-H23-N7-O5
MOLECULAR WEIGHT :
381.45

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
85GDA2 "CRC Handbook of Antibiotic Compounds," Vols.1- , Berdy, J., Boca Raton, FL, CRC Press, 1980- Volume(issue)/page/year: 5,298,1981
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
185 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JANTAJ Journal of Antibiotics. (Japan Antibiotics Research Assoc., 2-20-8 Kamiosaki, Shinagawa-ku, Tokyo, 141, Japan) V.2-5, 1948-52; V.21- 1968- Volume(issue)/page/year: 26,463,1973

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xn
Risk Phrases R22
Safety Phrases S36
RIDADR NONH for all modes of transport
RTECS HE3140000

 Synthetic Route

 Articles7

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 Synonyms

(2S,5S)-2,5-Diamino-6-[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]hexanoic acid (non-preferred name)
Sinefungin
D-Glycero-α-L-talo-Decofuranuronic acid, 6,9-diamino-1- (6-amino-9H-purin-9-yl)-1,5,6,7,8,9-hexadeoxy-
6,9-Diamino-1-(6-amino-9H-purin-9-yl)-1,5,6,7,8,9-hexadeoxy-D-glycero-a-L-talo-decofuranuronic Acid
Antibiotic 32232RP
(5S)-5-Amino-6-[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]-L-norleucine
(5S)-5-Amino-6-[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydro-2-furanyl]-L-norleucine
UNII:W2U467CIIL
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