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Hycanthone

Hycanthone ??? ???
?? ??:
3105-97-3
???:
Hycanthone
???(??):
ETRENOL;hycanthon;nsc-134434;Win 249-33;HYCANTHONE;Etrenol(mesylate);lucanthonemetabolite;Hycanthone, 10 mM in DMSO;1-(2-diethylaminoethylamino)-4-methylol-thioxanthen-9-one;1-((2-(diethylamino)ethyl)amino)-4-(hydroxymethyl)thioxanthen-9-one
CBNumber:
CB9181533
???:
C20H24N2O2S
??? ??:
356.48
MOL ??:
3105-97-3.mol

Hycanthone ??

???
100.6-102.8°
?? ?
570.5±50.0 °C(Predicted)
??
1.1269 (rough estimate)
???
1.6000 (estimate)
?? ??
Keep in dark place,Sealed in dry,2-8°C
???
DMSO : 30 mg/mL (84.16 mM)
?? ?? (pKa)
pKa 3.40 (Uncertain)
??? ??
Solid
??
Yellow to orange
EPA
Hycanthone (3105-97-3)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? T
?? ???? ?? 45-46-20/21/22
????? 53-36/37/39-45
WGK ?? 3
RTECS ?? XO1590000
????(GHS): Exclamation Mark (GHS07)Health Hazard (GHS08)
?? ?: Danger
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H302 ??? ??? ?? ?? ?? - ?? ?? 4 ?? P264, P270, P301+P312, P330, P501
H312 ??? ???? ??? ?? ?? ?? - ?? ?? 4 ?? P280,P302+P352, P312, P322, P363,P501
H332 ???? ??? ?? ?? ?? ?? ?? 4 ?? P261, P271, P304+P340, P312
H350 ?? ??? ? ?? (????? ?? ???? ???? ???? ??? ?? ????? ??? ???? ??) ??? ?? ?? 1A, 1B ??
??????:
P261 ??·?·??·???·??·...·????? ??? ????.
P264 ?? ??? ?? ??? ????.
P264 ?? ??? ?? ??? ????.
P270 ? ??? ??? ??? ???, ???? ???? ???.
P271 ?? ?? ??? ? ?? ???? ?????.
P280 ????/???/???/?????? ?????.
P301+P312 ??? ???? ??? ????(??)? ??? ????.
P302+P352 ??? ??? ??? ?? ????.
P304+P340 ???? ??? ??? ?? ??? ??? ???? ?? ??? ??? ????.
P312 ???? ??? ????(??)? ??? ????.
P322 ?? ??(??? … ??)
P330 ?? ?????.
P363 ?? ??? ??? ??? ?????.
P501 ...? ??? / ??? ?? ???.

Hycanthone C??? ??, ??, ??

??

Hycanthone is the active metabolite of the anthelmintic prodrug Lucanthone (L473700), which is used in the treatment of schistosomiasis.

??

ChEBI: A thioxanthen-9-one compound having a hydroxymethyl substituent at the 1-position and a 2-[(diethylamino)ethyl]amino substituent at the 4-position. It was formerly used (particularly as the monomethanesulfonic acid salt) as a schistosomicide for individual or mass treatement of infection with Schistosoma haematobium and S. mansoni, but due to its toxicity and concern about possible carcinogenicity, it has been replaced by other drugs such as praziquantel.

?? ??

Odorless canary yellow to yellow-orange crystalline powder. Bitter taste.

??? ?? ??

1-[(2-[DIETHYLAMINO]ETHYL)AMINO]-4-[HYDROXYMETHYL]-9H-THIOXANTHEN-9-ONE may be sensitive to prolonged exposure to air and light. Highly soluble in water.

?? ???

1-[(2-[DIETHYLAMINO]ETHYL)AMINO]-4-[HYDROXYMETHYL]-9H-THIOXANTHEN-9-ONE is very sensitive to acid. .

????

Flash point data for 1-[(2-[DIETHYLAMINO]ETHYL)AMINO]-4-[HYDROXYMETHYL]-9H-THIOXANTHEN-9-ONE are not available; however, 1-[(2-[DIETHYLAMINO]ETHYL)AMINO]-4-[HYDROXYMETHYL]-9H-THIOXANTHEN-9-ONE is probably combustible.

Safety Profile

Poison by subcutaneous, intravenous, and intramuscular routes. Moderately toxic by ingestion. Experimental teratogenic effects. Human mutation data reported. Questionable carcinogen with experimental carcinogenic data. When heated to decomposition it emits very toxic fumes of NOx and SOx.

Hycanthone ?? ?? ? ???

???

?? ??


Hycanthone ?? ??

???( 44)?? ??
??? ?? ??? ?? ?? ? ??
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Hycanthone ?? ??:

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