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
  • (S)-N-Methylquinuclidin-3-aminedihydrochloride
  • 8-(2-Chloro-4-fluorophenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amine
  • 1-(Benzylamino)cyclobutane-1-carboxylic acid
  • 2-(3-Bromobenzyl)-3-methylnaphthalene-1,4-dione
  • 5-(aminomethyl)-N,N-diethylpyridin-2-amine dihydrochloride
  • O-Ethyl-L-tyrosine methyl ester HCl
  • (2-Methoxyethyl)({[1-(2-methoxyethyl)cyclopentyl]methyl})amine
  • 2-(Octan-2-yloxy)ethane-1-sulfonyl chloride
  • 1-((Chloromethyl)sulfonyl)-N,N-dimethylpiperidin-3-amine
  • 1-(cyclopropylmethoxy)butan-2-amine
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