| Weight | 412.914 g/mol |
|---|---|
| Formula | C20H29ClN2O5 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 7 |
Ultiva (132539-07-2)
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LabBot
- Le rmifentanil (Ultiva): plus qu'un morphinique de plus (Annales Francaises D Anesthesie Et De Reanimation, 1997)
- [Esterase-metabolized remifentanil hydrochloride opioid (Ultiva-TM), a new step towards the solution of the problem of regulation of analgetic components of general anesthesia]. (Journal of Clinical Gastroenterology, 2001)
- Direct Effect of Remifentanil and Glycine Contained in Ultiva on Nociceptive Transmission in the Spinal Cord: In Vivo and Slice Patch Clamp Analyses. (PLOS ONE, 2016)
- New Indications for Ultiva (Southern African Journal of Anaesthesia and Analgesia, 2003)
- 732 REMIFENTANIL HYDROCHLORIDE (ULTIVA) CHOICE OF ANALGESIA IN AMBULATORY URETERORENOSCOPY (European Journal of Pain, 2006)
- Direct actions of Ultiva on dorsal horn neurons in the rat spinal cord revealed by patch clamp analysis: 7AP1-4 (European Journal of Anaesthesiology, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC(=O)N(C1=CC=CC=C1)C2(CCN(CC2)CCC(=O)OC)C(=O)OC.Cl
-
InChIKeyWFBMIPUMYUHANP-UHFFFAOYSA-N
- Pubchem - Ultiva
- Wikipedia - remifentanil hydrochloride
Remifentanil is a potent, short-acting synthetic opioid analgesic drug. It is given to patients during surgery to relieve pain and as an adjunct to an anaesthetic. Remifentanil is used for sedation as well as combined with other medications for use in general anesthesia.
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