acetylcarnitine

Small moleculeexperimental

Acetyl-L-carnitine, ALCAR or ALC, is an acetylated form of L-carnitine. It is naturally produced by the human body, and it is available as a dietary supplement. Acetylcarnitine is broken down in the blood by plasma esterases to carnitine which is used by the body to transport fatty acids into the mitochondria for breakdown and energy production. — Wikipedia

Clinical trial activity

37 trials · 54 clinical orgs · 0 marketing orgs

Phase 1
5
Phase 2
17
Phase 3
8
Phase 4
7

Earliest trial started Oct 1, 1997 (NCT01913964)

Timeline

2000s

  1. Jan 1, 2003

    Earliest Phase 2 Sponsor(trial)

  2. Jan 1, 2006

    Earliest Phase 1 Sponsor(trial)

  3. Jan 1, 2008

    Earliest Phase 3 Sponsor(trial)

Indications

Approved for

Mechanism of action

  • SLC33A1 activator

    L-Acetylcarnitine is an acetic acid ester of carnitine that facilitates movement of acetyl CoA into the matrices of mammalian mitochondria during the oxidation of fatty acids. In addition to its metabolic role, acetyl-L-carnitine posses unique neuroprotective, neuromodulatory, and neurotrophic properties that may play an important role in counteracting various disease processes. It is able to cross the bloodbrain barrier and enter the blood circulation in the brain. It shows a nicotinic action, principally at the neuromuscular junction, blocking the transmission. It has been demonstrated that acetate moieties of acetyl-L-carnitine play a role in increasing the potency of cholinergic and anticholinergic actions by reacting with the electrophilic or cationic site of the cholinergic receptor. It has also been reported that acetylcarnitine inhibits alcohol dehydrogenase competitively. (Acetylcarnitine competes with NAD+ (Ki = 135 mumol.L-1))

  • Unspecified targetOTHER

    Unknown

    L-Acetylcarnitine is an acetic acid ester of carnitine that facilitates movement of acetyl CoA into the matrices of mammalian mitochondria during the oxidation of fatty acids. In addition to its metabolic role, acetyl-L-carnitine posses unique neuroprotective, neuromodulatory, and neurotrophic properties that may play an important role in counteracting various disease processes. It is able to cross the bloodbrain barrier and enter the blood circulation in the brain. It shows a nicotinic action, principally at the neuromuscular junction, blocking the transmission. It has been demonstrated that acetate moieties of acetyl-L-carnitine play a role in increasing the potency of cholinergic and anticholinergic actions by reacting with the electrophilic or cationic site of the cholinergic receptor. It has also been reported that acetylcarnitine inhibits alcohol dehydrogenase competitively. (Acetylcarnitine competes with NAD+ (Ki = 135 mumol.L-1))

  • Unspecified targetUnknown

    Unknown

    L-Acetylcarnitine is an acetic acid ester of carnitine that facilitates movement of acetyl CoA into the matrices of mammalian mitochondria during the oxidation of fatty acids. In addition to its metabolic role, acetyl-L-carnitine posses unique neuroprotective, neuromodulatory, and neurotrophic properties that may play an important role in counteracting various disease processes. It is able to cross the bloodbrain barrier and enter the blood circulation in the brain. It shows a nicotinic action, principally at the neuromuscular junction, blocking the transmission. It has been demonstrated that acetate moieties of acetyl-L-carnitine play a role in increasing the potency of cholinergic and anticholinergic actions by reacting with the electrophilic or cationic site of the cholinergic receptor. It has also been reported that acetylcarnitine inhibits alcohol dehydrogenase competitively. (Acetylcarnitine competes with NAD+ (Ki = 135 mumol.L-1))

Chemistry & pharmacology

Loading structure…

SMILES

CC(=O)O[C@H](CC(=O)[O-])C[N+](C)(C)C
Mol. weight
203.24 g/mol
Lipinski Ro5
Pass
Rule of 3
No
Chirality
Single Stereoisomer
Inorganic
No
Polymer
No

Oral

No

Parenteral

No

Topical

No

Sources

Also known as

  • acetylcarnitine
  • acetylcarnitine
  • acetylcarnitine
  • acetylcarnitine
  • acetylcarnitine
  • acetylcarnitine
  • acetylcarnitine
  • acetylcarnitine
  • acetyl l-carnitine
  • acetyl l-carnitine
  • acetyl-l-carnitine
  • acetyl-l-carnitine
  • acetyl-l-carnitine
  • acetyl-l-carnitine
  • acetyl-l-carnitine hydrochloride
  • l acetyl carnitine
  • l acetyl carnitine
  • l-acetylcarnitine
  • l-acetylcarnitine
  • l-acetylcarnitine
  • l-acetyl carnitine
  • l-acetyl carnitine
  • levocarnitine acetyl
  • nicetile
  • nicetile
  • o-acetylcarnitine
  • o-acetylcarnitine
  • o-acetylcarnitine
  • o-acetyl-l-carnitine
  • o-acetyl-l-carnitine

Clinical trials

NCT IDPhaseStart dateSponsor(s)
NCT06126315Phase 2/Phase 3 (Phase 3)Jan 31, 2024FightMND, Mario Negri Institute, University of Sydney
NCT05653895N/ADec 7, 2022Khyber Medical University Peshawar, Khyber Medical University Peshawer
NCT05601479Phase 2Nov 1, 2022Southern Medical University
NCT05616000Phase 2Aug 6, 2022Khyber Medical University Peshawar
NCT05355311Phase 1Jun 30, 2022Brown University, Colorado State University, National Institute on Alcohol Abuse and Alcoholism (NIAAA), Rhode Island Hospital
NCT04623619N/ADec 15, 2020University of Palermo
NCT04509258Phase 4Oct 31, 2020Ain Shams University, Cairo University
NCT04113889Phase 4Oct 31, 2019Khyber Medical University Peshawar
NCT02971878N/ANov 1, 2016Fertilitetscentrum AB, Vitrolife
NCT02955706Phase 4Apr 1, 2016Dong-A Pharmaceutical, Konkuk University
NCT04346862Phase 4Jan 26, 2016Hanmi Pharmaceutical
NCT02141035Phase 2/Phase 3 (Phase 3)Sep 1, 2015University of Alberta
NCT02538146Early Phase 1 (Phase 1)Aug 1, 2015University of Kentucky
NCT01921868N/AAug 1, 2013University of South Florida
NCT01695317Phase 4Apr 1, 2013Norwegian National Headache Centre, Norwegian University of Science and Technology
NCT01492920Phase 3Apr 1, 2012Gynecologic Oncology Group, National Cancer Institute (NCI)
NCT01524861Phase 4Dec 1, 2011University of Campania Luigi Vanvitelli
NCT01379976Phase 3Apr 1, 2011Mario Negri Institute, University of Perugia
NCT01381354Phase 1Oct 1, 2010DJO Incorporated, Pinnaclife Inc., TZ Press, LLC, University of Iowa
NCT01537549Phase 1/Phase 2 (Phase 2)Sep 14, 2010Cornell University
Showing 20 of 37 trials
Page 1 / 2

Organizations

Research & Development (54)

OrganizationOrg typeTrialsAs lead sponsorPhasesEarliest year
University of CataniaAcademic/Hospital6631997
Khyber Medical University PeshawarAcademic/Hospital3332019
Mario Negri InstituteAcademic/Hospital3322004
National Cancer Institute (NCI)Government2012009
Ain Shams UniversityAcademic/Hospital1012020
BayerFor profit1112008
Bristol-Myers SquibbFor profit1012003
Brown UniversityAcademic/Hospital1112022
Cairo UniversityAcademic/Hospital1112020
Colorado State UniversityAcademic/Hospital1012022
Cornell UniversityAcademic/Hospital1112010
DJO IncorporatedFor profit1012010
Dong-A PharmaceuticalFor profit1112016
Fertilitetscentrum ABAcademic/Hospital1112016
FightMNDAcademic/Hospital1012024
Gynecologic Oncology GroupAcademic/Hospital1112012
Hanmi PharmaceuticalFor profit1112016
Indiana UniversityAcademic/Hospital1112009
Jiao Tong UniversityAcademic/Hospital1012008
Khyber Medical University PeshawerAcademic/Hospital1012022
54 organizations
Page 1 / 3