Triamcinolone hexacetonideProduct ingredient for Triamcinolone

Name
Triamcinolone hexacetonide
Drug Entry
Triamcinolone

Triamcinolone is a corticosteroid used to treat various inflammatory conditions in the body from allergic rhinitis to acute exacerbations of multiple sclerosis.13 Triamcinolone can be used as a one time adjunct treatment of osteoarthritic knee pain,16 or first line as a topical treatment of corticosteroid responsive dermatoses.11 Triamcinolone is more commonly seen in the forms triamcinolone hexacetonide, triamcinolone acetonide, and triamcinolone diacetate.10,11,12,13,14,15,16

Triamcinolone was granted FDA approval on 3 December 1957.9 In October 2021, a suspension of triamcinolone acetonide was approved for suprachoroidal injection - the first suprachoroidal injection to receive FDA approval19 - for the treatment of patients with macular edema associated with uveitis.18

Accession Number
DBSALT000861
Structure
Synonyms
Hexacetonido de triancinolona / Triamcinolone hexacetonide / Triamcinoloni hexacetonidum
External IDs
BRN 1413888 / CL 34433 / CL-34433
UNII
I7GT1U99Y9
CAS Number
5611-51-8
Weight
Average: 532.649
Monoisotopic: 532.283631823
Chemical Formula
C30H41FO7
InChI Key
TZIZWYVVGLXXFV-FLRHRWPCSA-N
InChI
InChI=1S/C30H41FO7/c1-25(2,3)15-24(35)36-16-22(34)30-23(37-26(4,5)38-30)13-20-19-9-8-17-12-18(32)10-11-27(17,6)29(19,31)21(33)14-28(20,30)7/h10-12,19-21,23,33H,8-9,13-16H2,1-7H3/t19-,20-,21-,23+,27-,28-,29-,30+/m0/s1
IUPAC Name
2-[(1S,2S,4R,8S,9S,11S,12R,13S)-12-fluoro-11-hydroxy-6,6,9,13-tetramethyl-16-oxo-5,7-dioxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosa-14,17-dien-8-yl]-2-oxoethyl 3,3-dimethylbutanoate
SMILES
[H][C@@]12C[C@H]3OC(C)(C)O[C@@]3(C(=O)COC(=O)CC(C)(C)C)[C@@]1(C)C[C@H](O)[C@@]1(F)[C@@]2([H])CCC2=CC(=O)C=C[C@]12C
KEGG Drug
D00985
KEGG Compound
C08185
PubChem Compound
21826
ChemSpider
20516
ChEBI
9670
ChEMBL
CHEMBL1200878
ZINC
ZINC000004097475
Wikipedia
Triamcinolone_hexacetonide
Predicted Properties
PropertyValueSource
Water Solubility0.00314 mg/mLALOGPS
logP3.9ALOGPS
logP4.12Chemaxon
logS-5.2ALOGPS
pKa (Strongest Acidic)13.63Chemaxon
pKa (Strongest Basic)-3.4Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count6Chemaxon
Hydrogen Donor Count1Chemaxon
Polar Surface Area99.13 Å2Chemaxon
Rotatable Bond Count6Chemaxon
Refractivity138.99 m3·mol-1Chemaxon
Polarizability56.04 Å3Chemaxon
Number of Rings5Chemaxon
Bioavailability1Chemaxon
Rule of FiveNoChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleYesChemaxon