| Compound Information | SONAR Target prediction |
| Name: | AZELAIC ACID |
| Unique Identifier: | SPE01500648 |
| MolClass: | Checkout models in ver1.5 and ver1.0 |
| Molecular Formula: | |
| Molecular Weight: | 172.094 g/mol |
| X log p: | -1.656 (online calculus) |
| Lipinksi Failures | 0 |
| TPSA | 34.14 |
| Hydrogen Bond Donor Count: | 0 |
| Hydrogen Bond Acceptors Count: | 4 |
| Rotatable Bond Count: | 8 |
| Canonical Smiles: | OC(=O)CCCCCCCC(O)=O |
| Class: | alkane |
| Source: | rancid fats and Lycopodium spp |
| Therapeutics: | antiacne, antiproliferative agent |
| Generic_name: | Azelaic Acid |
| Chemical_iupac_name: | nonanedioic acid |
| Drug_type: | Approved Drug |
| Pharmgkb_id: | PA448516 |
| Kegg_compound_id: | C08261 |
| Drugbank_id: | APRD00812 |
| Melting_point: | 106.5 oC |
| H2o_solubility: | 2400 mg/L (20°C) |
| Logp: | 1.646 |
| Isoelectric_point: | 4.55 |
| Cas_registry_number: | 123-99-9 |
| Mass_spectrum: | http://webbook.nist.gov/cgi/cbook.cgi?Spec=C123999&Index=0&Type=Mass&Large=on |
| Drug_category: | Antineoplastic Agents; Dermatologic Agents; ATC:D10AX03 |
| Indication: | For the topical treatment of mild-to-moderate inflammatory acne vulgaris. |
| Pharmacology: | Azelaic acid is a saturated dicarboxylic acid found naturally in wheat, rye, and barley. It is a natural substance that is produced by Malassezia furfur (also known as Pityrosporum ovale), a yeast that lives on normal skin. It is effective against a number of skin conditions, such as mild to moderate acne, when applied topically in a cream formulation of 20%. It works in part by stopping the growth of skin bacteria that cause acne, and by keeping skin pores clear. Azelaic acid-s antimicrobial action may be attributable to inhibition of microbial cellular protein synthesis. |
| Mechanism_of_action: | The exact mechanism of action of azelaic acid is not known. It is thought that azelaic acid manifests its antibacterial effects by inhibiting the synthesis of cellular protein in anaerobic and aerobic bacteria, especially Staphylococcus epidermidis and Propionibacterium acnes. In aerobic bacteria, azelaic acid reversibly inhibits several oxidoreductive enzymes including tyrosinase, mitochondrial enzymes of the respiratory chain, thioredoxin reductase, 5-alpha-reductase, and DNA polymerases. In anaerobic bacteria, azelaic acid impedes glycolysis. Along with these actions, azelaic acid also improves acne vulgaris by normalizing the keratin process and decreasing microcomedo formation. Azelaic acid may be effective against both inflamed and noninflamed lesions. Specifically, azelaic acid reduces the thickness of the stratum corneum, shrinks keratohyalin granules by reducing the amount and distribution of filaggrin (a component of keratohyalin) in epidermal layers, and lowers the number of keratohyalin granules. |
| Organisms_affected: | Various aerobic and anaerobic microorganisms |
| Found: 205 nonactive as graph: single | with analogs | [1] << Back 191 192 193 194 195 196 197 198 199 200 Next >> [205] |
| Species: | 4932 |
| Condition: | SWE1 |
| Replicates: | 2 |
| Raw OD Value: r im | 0.7864±0.00643467 |
| Normalized OD Score: sc h | 0.9917±0.00324933 |
| Z-Score: | -0.7145±0.0391468 |
| p-Value: | 0.475092 |
| Z-Factor: | -2.81955 |
| Fitness Defect: | 0.7442 |
| Bioactivity Statement: | Nonactive |
| ps |
| DBLink | Rows returned: 2052 | [1] << Back 1 2 3 4 5 6 7 8 9 10 Next >> [342] |
| 3893 | dodecanoic acid |
| 5192 | decanedioic acid |
| 5281 | octadecanoic acid |
| 6742 | 4-[(3R,5R,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tet radecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid |
| 7413 | cyclohexanecarboxylic acid |
| 7789 | 12-hydroxyoctadecanoic acid |
| internal high similarity DBLink | Rows returned: 29 | 1 2 3 4 5 Next >> |
| JFD 01238 | 0.9524 |
| SPE01500840 | 0.9524 |
| SPE01500837 | 0.9524 |
| SPE01500605 | 0.9524 |
| SPE01500225 | 0.9524 |
| SPE00270049 | 0.9524 |
| active | Cluster 13528 | Additional Members: 3 | Rows returned: 0 |
Service provided by the
Mike Tyers Laboratory