Austricin

Details

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Internal ID 8add9b1c-da38-452a-9645-bfd6bc06def4
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3S,3aR,4S,9aS,9bR)-4-hydroxy-3,6,9-trimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2,7-dione
SMILES (Canonical) CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)O
SMILES (Isomeric) C[C@H]1[C@@H]2[C@H](CC(=C3[C@@H]([C@H]2OC1=O)C(=CC3=O)C)C)O
InChI InChI=1S/C15H18O4/c1-6-4-10(17)13-8(3)15(18)19-14(13)12-7(2)5-9(16)11(6)12/h5,8,10,12-14,17H,4H2,1-3H3/t8-,10-,12-,13+,14+/m0/s1
InChI Key YMUOZXZDDBRJEP-XUNJKSNWSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O4
Molecular Weight 262.30 g/mol
Exact Mass 262.12050905 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.39
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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Desacetylmatricarin
Hydroxyachillin
10180-88-8
Matricarin, deacetyl-
Deacetylmatricarin
8-Deacetylmatricarin
8P8G4SWG5Y
NSC 180030
NSC-180030
(3S,3aR,4S,9aS,9bR)-4-hydroxy-3,6,9-trimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2,7-dione
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Austricin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9898 98.98%
Caco-2 + 0.5247 52.47%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5333 53.33%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.9413 94.13%
OATP1B3 inhibitior + 0.9563 95.63%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9304 93.04%
P-glycoprotein inhibitior - 0.9166 91.66%
P-glycoprotein substrate - 0.8122 81.22%
CYP3A4 substrate + 0.5189 51.89%
CYP2C9 substrate - 0.7791 77.91%
CYP2D6 substrate - 0.8897 88.97%
CYP3A4 inhibition - 0.8705 87.05%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9256 92.56%
CYP2D6 inhibition - 0.9593 95.93%
CYP1A2 inhibition - 0.7028 70.28%
CYP2C8 inhibition - 0.9303 93.03%
CYP inhibitory promiscuity - 0.9617 96.17%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Danger 0.4320 43.20%
Eye corrosion - 0.9486 94.86%
Eye irritation - 0.6674 66.74%
Skin irritation - 0.5342 53.42%
Skin corrosion - 0.8918 89.18%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6525 65.25%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.6587 65.87%
skin sensitisation - 0.7302 73.02%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.6645 66.45%
Acute Oral Toxicity (c) II 0.3903 39.03%
Estrogen receptor binding - 0.7810 78.10%
Androgen receptor binding + 0.5715 57.15%
Thyroid receptor binding - 0.6070 60.70%
Glucocorticoid receptor binding - 0.6527 65.27%
Aromatase binding - 0.9064 90.64%
PPAR gamma - 0.8415 84.15%
Honey bee toxicity - 0.8628 86.28%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.8782 87.82%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.46% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.41% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.91% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.58% 94.80%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.86% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 87.36% 86.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.78% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.00% 90.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.53% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.34% 96.09%

Cross-Links

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PubChem 6713966
NPASS NPC165287
LOTUS LTS0257722
wikiData Q27164845