5,6-Dehydroeurycomalactone

Details

Top
Internal ID 1eef5d48-6304-440d-a379-71cad5b14bac
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones
IUPAC Name (1S,2R,9S,10R,11R,12R,13R,16R)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.02,11.05,10]hexadeca-4,6-diene-3,8,15-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H22O6/c1-7-5-10(20)16(23)18(3)9(7)6-11(21)19(4)12-8(2)14(25-17(12)24)13(22)15(18)19/h5-6,8,12-16,22-23H,1-4H3/t8-,12-,13+,14-,15-,16-,18+,19+/m1/s1
InChI Key PKCDREAJEQQORV-FMXIYLAGSA-N
Popularity 5 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H22O6
Molecular Weight 346.40 g/mol
Exact Mass 346.14163842 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.57
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

Top
CHEMBL1081240
SCHEMBL29361746

2D Structure

Top
2D Structure of 5,6-Dehydroeurycomalactone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9864 98.64%
Caco-2 - 0.7888 78.88%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7246 72.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8537 85.37%
OATP1B3 inhibitior + 0.9286 92.86%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8699 86.99%
P-glycoprotein inhibitior - 0.7774 77.74%
P-glycoprotein substrate - 0.6863 68.63%
CYP3A4 substrate + 0.6155 61.55%
CYP2C9 substrate - 0.7828 78.28%
CYP2D6 substrate - 0.8976 89.76%
CYP3A4 inhibition - 0.8254 82.54%
CYP2C9 inhibition - 0.8459 84.59%
CYP2C19 inhibition - 0.9115 91.15%
CYP2D6 inhibition - 0.9211 92.11%
CYP1A2 inhibition - 0.7029 70.29%
CYP2C8 inhibition - 0.8329 83.29%
CYP inhibitory promiscuity - 0.6721 67.21%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Danger 0.5326 53.26%
Eye corrosion - 0.9774 97.74%
Eye irritation - 0.9026 90.26%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9116 91.16%
Ames mutagenesis - 0.5970 59.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6300 63.00%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.5815 58.15%
skin sensitisation - 0.7119 71.19%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6641 66.41%
Acute Oral Toxicity (c) III 0.5250 52.50%
Estrogen receptor binding + 0.7736 77.36%
Androgen receptor binding + 0.6263 62.63%
Thyroid receptor binding - 0.5084 50.84%
Glucocorticoid receptor binding + 0.5733 57.33%
Aromatase binding - 0.6279 62.79%
PPAR gamma - 0.5898 58.98%
Honey bee toxicity - 0.8287 82.87%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9722 97.22%

Targets

Top

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.78% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.77% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.87% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.66% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.75% 99.23%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.26% 86.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.75% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.56% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.97% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 80.52% 94.73%

Cross-Links

Top
PubChem 15173195
NPASS NPC210005
ChEMBL CHEMBL1081240
LOTUS LTS0198988
wikiData Q105210306