Details
Stereochemistry | EPIMERIC |
Molecular Formula | C6H8O6.C4H6N4O3 |
Molecular Weight | 334.2396 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)NC1NC(=O)NC1=O.[H][C@@]2(OC(=O)C(O)=C2O)[C@@H](O)CO
InChI
InChIKey=BMZVXYKKNCVBBF-RXSVEWSESA-N
InChI=1S/C6H8O6.C4H6N4O3/c7-1-2(8)5-3(9)4(10)6(11)12-5;5-3(10)6-1-2(9)8-4(11)7-1/h2,5,7-10H,1H2;1H,(H3,5,6,10)(H2,7,8,9,11)/t2-,5+;/m0./s1
DescriptionSources: http://biotechnologia.pl/uploads/biotechnologia/product/leaflet/156476/info_20ALCLOXA.pdfhttp://www.rad-ar.or.jp/siori/english/kekka_plain.cgi?n=34714 | https://www.ncbi.nlm.nih.gov/pubmed/26620883Curator's Comment: description was created based on several sources, including:
http://tri-k.com/acloxa
Sources: http://biotechnologia.pl/uploads/biotechnologia/product/leaflet/156476/info_20ALCLOXA.pdfhttp://www.rad-ar.or.jp/siori/english/kekka_plain.cgi?n=34714 | https://www.ncbi.nlm.nih.gov/pubmed/26620883
Curator's Comment: description was created based on several sources, including:
http://tri-k.com/acloxa
Aldioxa is the generic name for the metal complex, dihydroxyaluminum allantoinate, which is hydrolyzed to allantoin and aluminium hydrate at the gastric mucosa. Aldioxa was approved in Japan to improve subjective symptoms or objective of gastric/duodenal ulcer and gastritis. It was discovered, that aldioxa ameliorates delayed gastric emptying through its antagonistic activity on the α-2 adrenergic receptor. The most commonly reported adverse reactions include constipation.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL1867 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26620883 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Preventing | BODYGLIDE FOR HER Approved Usehelps prevent and helps relieve chafed, chapped or cracked skin. helps protect from the drying effects of wind and cold weather. temporarily protects minor cuts, scrapes, burns. Launch Date2009 |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved Useprotects gastric / duodenal tissue mucosa and helps repair, thus improving gastric / duodenal ulcer and gastritis. It is usually used to improve subjective symptoms or objective of gastric/duodenal ulcer and gastritis. |
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Primary | Unknown Approved Useprotects gastric / duodenal tissue mucosa and helps repair, thus improving gastric / duodenal ulcer and gastritis. It is usually used to improve subjective symptoms or objective of gastric/duodenal ulcer and gastritis. |
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Primary | Unknown Approved Useprotects gastric / duodenal tissue mucosa and helps repair, thus improving gastric / duodenal ulcer and gastritis. It is usually used to improve subjective symptoms or objective of gastric/duodenal ulcer and gastritis. |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
6.43 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/9131540/ |
10 mg/kg 3 times / day steady-state, oral dose: 10 mg/kg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALLANTOIN plasma | Canis lupus population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
30 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/9131540/ |
10 mg/kg 3 times / day steady-state, oral dose: 10 mg/kg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALLANTOIN plasma | Canis lupus population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
2.69 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/9131540/ |
10 mg/kg 3 times / day steady-state, oral dose: 10 mg/kg route of administration: Oral experiment type: STEADY-STATE co-administered: |
ALLANTOIN plasma | Canis lupus population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
Sample Use Guides
Antiperspirants, deodorants: Creams, spray, lossions: 0.25-0.5%
Baby products: creams; powders: 0.2-0.5%
Route of Administration:
Topical
In vitro Alcloxa inhibited formation and bacterial decomposition of pulverized human epidermal scales. The scales were obtained from patient with exfoliative dermatitis, characterized by a great deal of exudation. The scales were were pulverized in a Wiley mill, defatted with ether and suspended in a 0,2% Alcloxa solution.
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67732897
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127941-88-2
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76WX3J5GER
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76WX3J5GER
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DTXSID90972924
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2559842
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57448-83-6
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260-739-1
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PARENT (SALT/SOLVATE)
SUBSTANCE RECORD