16-O-acetylgitoxin

Names

[ CAS No. ]:
7242-07-1

[ Name ]:
16-O-acetylgitoxin

[Synonym ]:
16-acetyl-gitoxin
29 Na 4
gitoxin 16-acetate
Einecs 230-646-0
ACETYLGITOXIN,16
16-ACETYLGITOXIN
336 N
acetyl-16-gitoxine

Chemical & Physical Properties

[ Density]:
1.34g/cm3

[ Boiling Point ]:
359.8ºC at 760 mmHg

[ Molecular Formula ]:
C43H66O15

[ Molecular Weight ]:
822.97500

[ Flash Point ]:
171.4ºC

[ Exact Mass ]:
822.44000

[ PSA ]:
209.13000

[ LogP ]:
2.78890

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
LZ0875000
CHEMICAL NAME :
Gitoxin, 16-acetate
CAS REGISTRY NUMBER :
7242-07-1
LAST UPDATED :
199109
DATA ITEMS CITED :
7
MOLECULAR FORMULA :
C43-H66-O15
MOLECULAR WEIGHT :
823.09
WISWESSER LINE NOTATION :
L E5 B666TJ A1 E1 GQ IOV1 F- DT5OV EHJ& OO- FT6OTJ B1 DQ CO- FT6OTJ B1 DQ CO- FT6OTJ B1 CQ DQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
16500 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
AIPTAK Archives Internationales de Pharmacodynamie et de Therapie. (Heymans Institute of Pharmacology, De Pintelaan 185, B-9000 Ghent, Belgium) V.4- 1898- Volume(issue)/page/year: 155,165,1965
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
6800 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
AIPTAK Archives Internationales de Pharmacodynamie et de Therapie. (Heymans Institute of Pharmacology, De Pintelaan 185, B-9000 Ghent, Belgium) V.4- 1898- Volume(issue)/page/year: 155,165,1965
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Mammal - cat
DOSE/DURATION :
120 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
AIPTAK Archives Internationales de Pharmacodynamie et de Therapie. (Heymans Institute of Pharmacology, De Pintelaan 185, B-9000 Ghent, Belgium) V.4- 1898- Volume(issue)/page/year: 159,1,1966
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Mammal - cat
DOSE/DURATION :
148 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
AIPTAK Archives Internationales de Pharmacodynamie et de Therapie. (Heymans Institute of Pharmacology, De Pintelaan 185, B-9000 Ghent, Belgium) V.4- 1898- Volume(issue)/page/year: 155,165,1965
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Mammal - cat
DOSE/DURATION :
610 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
85ELDJ "Die Herzwirksamen Glykoside," Baumgarten, G., and W. Forster, Leipzig, Ger. Dem. Rep., VEB Georg Thieme, 1963 Volume(issue)/page/year: -,187,1963
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - guinea pig
DOSE/DURATION :
2500 ug/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
AIPTAK Archives Internationales de Pharmacodynamie et de Therapie. (Heymans Institute of Pharmacology, De Pintelaan 185, B-9000 Ghent, Belgium) V.4- 1898- Volume(issue)/page/year: 159,1,1966 *** REVIEWS *** TOXICOLOGY REVIEW 85ELDJ "Die Herzwirksamen Glykoside," Baumgarten, G., and W. Forster, Leipzig, Ger. Dem. Rep., VEB Georg Thieme, 1963 Volume(issue)/page/year: -,187,1963

Synthetic Route

Precursor & DownStream

Precursor

  • gitoxin 3''',4'''-cyclocarbonate
  • GITOXIN

DownStream


Related Compounds

  • 16-O-Acetylvindoline
  • 16-O-Acetylpolyporenic acid C
  • 16-O-Methylcafestol
  • 16-o-acetyldarutigenol
  • 16-O-deacetylfusidic acid
  • 16-O-Methyl-14,15-didehydroisovincanol
  • Benzyl 2-(2-fluoro-5-methoxyphenyl)-2-hydroxy-7-azaspiro[3.5]nonane-7-carboxylate
  • 2-(Difluoromethyl)-4-methoxy-6-methylpyridine-3-acetonitrile
  • 7-(3-Methoxy-4-nitrophenyl)-2-methyl-2,7-diazaspiro[3.5]nonane
  • Tert-butyl 9-(2-chloro-5-methoxy-4-nitrophenyl)-3,9-diazaspiro[5.5]undecane-3-carboxylate
  • 3-(2-Fluoro-5-methoxy-4-nitrophenyl)-9-methyl-3,9-diazaspiro[5.5]undecane
  • 3-(4-Methoxy-5-nitro-2-pyridinyl)-9-methyl-3,9-diazaspiro[5.5]undecane
  • 2,5-Dichloro-N-[2-(dimethylphosphinyl)-6-fluorophenyl]-4-pyrimidinamine
  • 4-Methoxy-6-(9-methyl-3,9-diazaspiro[5.5]undec-3-yl)-3-pyridinamine
  • 4-(Difluoromethyl)-5-iodo-2-methylpyridine
  • 1-(2-Ethylphenyl)-1,5,6,7-tetrahydro-3,6,6-trimethyl-4H-indazol-4-one
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