| Weight | 244.294 g/mol |
|---|---|
| Formula | C14H16N2O2 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Etomidate (15301-65-2, 33125-97-2)
Ethomidate · Radenarkon · Hypnomidate
Score:
#108 in Neurology
,
#518 in Neuroscience
,
#2394 in Biology
,
#2969 in Chemistry
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- Inhibition of Adrenal Steroidogenesis by the Anesthetic Etomidate (The New England Journal of Medicine, 1984)
- The interaction of the general anesthetic etomidate with the gamma-aminobutyric acid type A receptor is influenced by a single amino acid. (Proceedings of the National Academy of Sciences of the United States of America, 1997)
- Sympathetic Responses to Induction of Anesthesia in Humans with Propofol or Etomidate (Anesthesiology, 1992)
- Etomidate versus ketamine for rapid sequence intubation in acutely ill patients: a multicentre randomised controlled trial (The Lancet, 2009)
- Identification of a GABAA Receptor Anesthetic Binding Site at Subunit Interfaces by Photolabeling with an Etomidate Analog (The Journal of Neuroscience, 2006)
- Adrenocortical function in critically ill patients 24 h after a single dose of etomidate. (Anaesthesia, 1999)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Ethomidate
- Radenarkon
- Hypnomidate
- R-26490
- R26490
- R 26490
-
SMILESCCOC(=O)C1=CN=CN1C(C)C2=CC=CC=C2
-
InChIKeyNPUKDXXFDDZOKR-UHFFFAOYSA-N
- Pubchem - Etomidate
- Wikipedia - etomidate
Etomidate (USAN, INN, BAN) (marketed as Amidate) is a short-acting intravenous anaesthetic agent used for the induction of general anaesthesia and sedation for short procedures such as reduction of dislocated joints, tracheal intubation, and cardioversion. It was developed at Janssen Pharmaceutica in 1964 and was introduced as an intravenous agent in 1972 in Europe and in 1983 in the United States.
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