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Details

Stereochemistry ACHIRAL
Molecular Formula C8H14NO3.Na
Molecular Weight 195.1914
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACEXAMATE SODIUM

SMILES

[Na+].CC(=O)NCCCCCC([O-])=O

InChI

InChIKey=UIEHVVUIWRNUKL-UHFFFAOYSA-M
InChI=1S/C8H15NO3.Na/c1-7(10)9-6-4-2-3-5-8(11)12;/h2-6H2,1H3,(H,9,10)(H,11,12);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula C8H14NO3
Molecular Weight 172.2017
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: The description was created based on several sources, including https://www.drugs.com/international/acexamic-acid.html | https://www.ncbi.nlm.nih.gov/pubmed/18353035 | https://www.ncbi.nlm.nih.gov/pubmed/6159453 | https://www.ncbi.nlm.nih.gov/pubmed/19470000

Acexamic acid (N-acetyl-amino-6-hexanoic acid) is a drug used as a cicatrization helper. Some studies show that the acexamic acid prevents the formation the connective inflamed tissue and enables its healing. The association from acexamic acid with zinc, zinc acexamate, has been used in the treatment of gastric and duodenal ulcer and in the prevention of gastric ulcer induced by nonsteroidal anti-inflammatory drugs.

Originator

Sources: Zeitschrift fuer Naturforschung (1947), 2b, 182-4

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Acemin ointment

Approved Use

Long-lasting non-healing wounds, skin and mucous burns, chronic traumatic osteomyelitis, closed and long-lasting incomplete fractures of bones, prevention of hyper-scarring, acceleration of the formation of a postoperative cosmetic scar, acceleration of engraftment of auto- and homotransplants.
Curative
Acemin ointment

Approved Use

Long-lasting non-healing wounds, skin and mucous burns, chronic traumatic osteomyelitis, closed and long-lasting incomplete fractures of bones, prevention of hyper-scarring, acceleration of the formation of a postoperative cosmetic scar, acceleration of engraftment of auto- and homotransplants.
PubMed

PubMed

TitleDatePubMed
Increase in bone growth factors with healing rat fractures: the enhancing effect of zinc.
2001 Oct
Alteration in serum and bone component findings induced in streptozotocin-diabetic rats is restored by zinc acexamate.
2003 Dec
Great increase in bone 66 kDa protein and osteocalcin at later stages with healing rat fractures: effect of zinc treatment.
2003 Feb
Preventive effect of zinc acexamate administration in streptozotocin-diabetic rats: Restoration of bone loss.
2003 Nov
[Nickel and magnesium effects in the rat kidney, treated with acid retinoic. Comparative study].
2007 Jul-Sep
Pharmacokinetics and first-pass effects of epsilon-acetamidocaproic acid after administration of zinc acexamate in rats.
2010 Jul
Performance of human immunostimulating agents in the improvement of fish cytogenetic preparations.
2010 Sep 14
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: http://www.lsgeotar.ru/atsexamovaya-kislota.html
Outer: 5% ointment is applied to the disinfected wound surface daily. The course of treatment is from 10 to 30 days.
Route of Administration: Topical
The mouse fibroblast cell line (NCTC Clone L 929) was maintained as stock culture in a minimum essential medium (MEM) supplemented with 10% calf serum and 200 i.u./ml G penicillin and 100 pg/d streptomycin. Cultures for growth studies were established by inoculating 7 X l0^4 cells in 2 ml medium in 35-mm plastic tissue culture dishes. They were maintained for 24 h to obtain a good attachment, then incubated in 5% calf serum medium supplemented or not with the drugs tested. Acexamic acid increased the growth rate of L 929 when used at a concentration of 0.001%
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:15:12 UTC 2023
Edited
by admin
on Fri Dec 15 17:15:12 UTC 2023
Record UNII
ZNY360XK9J
Record Status Validated (UNII)
Record Version
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Name Type Language
ACEXAMATE SODIUM
Common Name English
Sodium acexamate [WHO-DD]
Common Name English
.EPSILON.-ACETAMIDOCAPROIC ACID SODIUM SALT [MI]
Common Name English
EPSILON-ACETAMIDOCAPROIC ACID SODIUM SALT
Common Name English
.EPSILON.-ACETAMIDOCAPROIC ACID SODIUM SALT
MI  
Common Name English
Code System Code Type Description
FDA UNII
ZNY360XK9J
Created by admin on Fri Dec 15 17:15:12 UTC 2023 , Edited by admin on Fri Dec 15 17:15:12 UTC 2023
PRIMARY
CAS
7234-48-2
Created by admin on Fri Dec 15 17:15:12 UTC 2023 , Edited by admin on Fri Dec 15 17:15:12 UTC 2023
PRIMARY
ECHA (EC/EINECS)
230-635-0
Created by admin on Fri Dec 15 17:15:12 UTC 2023 , Edited by admin on Fri Dec 15 17:15:12 UTC 2023
PRIMARY
SMS_ID
100000078811
Created by admin on Fri Dec 15 17:15:12 UTC 2023 , Edited by admin on Fri Dec 15 17:15:12 UTC 2023
PRIMARY
EVMPD
SUB00280MIG
Created by admin on Fri Dec 15 17:15:12 UTC 2023 , Edited by admin on Fri Dec 15 17:15:12 UTC 2023
PRIMARY
MERCK INDEX
m1316
Created by admin on Fri Dec 15 17:15:12 UTC 2023 , Edited by admin on Fri Dec 15 17:15:12 UTC 2023
PRIMARY Merck Index
PUBCHEM
23665999
Created by admin on Fri Dec 15 17:15:12 UTC 2023 , Edited by admin on Fri Dec 15 17:15:12 UTC 2023
PRIMARY
RXCUI
236526
Created by admin on Fri Dec 15 17:15:12 UTC 2023 , Edited by admin on Fri Dec 15 17:15:12 UTC 2023
PRIMARY RxNorm
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY