Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C18H23N5O3.ClH |
Molecular Weight | 393.868 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.C[C@H](NCCN1C=NC2=C1C(=O)N(C)C(=O)N2C)[C@H](O)C3=CC=CC=C3
InChI
InChIKey=UTTZHZDGHMJDPM-NXCSSKFKSA-N
InChI=1S/C18H23N5O3.ClH/c1-12(15(24)13-7-5-4-6-8-13)19-9-10-23-11-20-16-14(23)17(25)22(3)18(26)21(16)2;/h4-8,11-12,15,19,24H,9-10H2,1-3H3;1H/t12-,15-;/m0./s1
Cafedrine, also known as norephedrinoethyltheophylline, is a chemical linkage of norephedrine and theophylline and is a cardiac stimulant used to increase blood pressure in people with hypotension. There are few data available for cafedrine. Cafedrine has a half-life of 60 min following both oral and intravenous administration Cafedrine is metabolized to norephedrine and several minor metabolites, but nearly 90% of the administered norephedrine is excreted via the kidneys, mostly unchanged, within 24 h. The effects of cafedrine on cardiac output are believed to be mediated via β- adrenoceptors. Cafedrine has a positive inotropic effect in humans, and this can be abolished by administration of the non-selective β-adrenoceptor antagonist propranolol. A combination of cafedrine and theodrenaline called Akrinor® is used for the treatment of hypotension in adults that occurs during emergency situations, general anesthesia, and regional anesthesia, especially during cesarean sections. Cafedrine/theodrenaline may have advantages over other vasopressor drugs. For example, it can be administered via bolus while catecholamines normally need to be diluted and administered via syringe pumps. Bolus injection is faster, which may be beneficial in emergency situations, plus it is more cost efficient with respect to the disposables. Cafedrine/theodrenaline has been widely used in Germany since 1963
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
[Spinal anesthesia for cesarean section]. | 2001 Jan |
|
[Mydriasis not reacting to light during an uneventful esophagectomy--drug-related side effect of Akrinor?]. | 2003 Mar |
|
Anesthetic management of a patient with histiocytosis X and pulmonary complications during Caesarean section. | 2004 Nov |
|
How to distinguish between ischemic and nonischemic postsystolic thickening: a strain rate imaging study. | 2006 Jan |
|
[Ephedrine as alternative to Akrinor in regional obstetric anesthesia]. | 2006 Jul |
|
[Old drugs and new approval procedures: Akrinor remains marketable and an application for reapproval of Arginin Vasopressin has been made]. | 2006 Jun |
|
Akrinor-induced relaxation of pig coronary artery in vitro is transformed into alpha1-adrenoreceptor-mediated contraction by pretreatment with propranolol. | 2006 Mar |
|
[Preoperative administration of angiotensin-converting enzyme inhibitors]. | 2007 Jun |
|
Glioblastoma cells express functional cell membrane receptors activated by daily used medical drugs. | 2009 Dec |
|
Clinical efficacy of beta1 selective adrenergic blockers in the treatment of neurocardiogenic syncope - a meta-analysis. | 2010 |
|
Impact of cafedrine/theodrenaline (Akrinor® ) on therapy of maternal hypotension during spinal anesthesia for Cesarean delivery: a retrospective study. | 2010 Dec |
Patents
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
5492688
Created by
admin on Fri Dec 15 17:34:14 GMT 2023 , Edited by admin on Fri Dec 15 17:34:14 GMT 2023
|
PRIMARY | |||
|
100000088420
Created by
admin on Fri Dec 15 17:34:14 GMT 2023 , Edited by admin on Fri Dec 15 17:34:14 GMT 2023
|
PRIMARY | |||
|
SUB00934MIG
Created by
admin on Fri Dec 15 17:34:14 GMT 2023 , Edited by admin on Fri Dec 15 17:34:14 GMT 2023
|
PRIMARY | |||
|
DTXSID20952734
Created by
admin on Fri Dec 15 17:34:14 GMT 2023 , Edited by admin on Fri Dec 15 17:34:14 GMT 2023
|
PRIMARY | |||
|
221-243-0
Created by
admin on Fri Dec 15 17:34:14 GMT 2023 , Edited by admin on Fri Dec 15 17:34:14 GMT 2023
|
PRIMARY | |||
|
L0N3M64B9R
Created by
admin on Fri Dec 15 17:34:14 GMT 2023 , Edited by admin on Fri Dec 15 17:34:14 GMT 2023
|
PRIMARY | |||
|
3039-97-2
Created by
admin on Fri Dec 15 17:34:14 GMT 2023 , Edited by admin on Fri Dec 15 17:34:14 GMT 2023
|
PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD