4-[2-[(1S,2R,4aS,8aR)-4a-(hydroxymethyl)-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-2H-furan-5-one

Details

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Internal ID 56faaf31-84f9-437c-8791-6e95918de508
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name 4-[2-[(1S,2R,4aS,8aR)-4a-(hydroxymethyl)-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O3/c1-14-7-11-20(13-21)15(2)5-4-6-17(20)19(14,3)10-8-16-9-12-23-18(16)22/h5,9,14,17,21H,4,6-8,10-13H2,1-3H3/t14-,17-,19+,20-/m1/s1
InChI Key SJXNVMMRISEMQM-SIKIZQCASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O3
Molecular Weight 318.40 g/mol
Exact Mass 318.21949481 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.02
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-[2-[(1S,2R,4aS,8aR)-4a-(hydroxymethyl)-1,2,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-2H-furan-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.8577 85.77%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6504 65.04%
OATP2B1 inhibitior - 0.8635 86.35%
OATP1B1 inhibitior + 0.8823 88.23%
OATP1B3 inhibitior + 0.9239 92.39%
MATE1 inhibitior - 0.7812 78.12%
OCT2 inhibitior + 0.5898 58.98%
BSEP inhibitior + 0.8226 82.26%
P-glycoprotein inhibitior - 0.7619 76.19%
P-glycoprotein substrate - 0.7989 79.89%
CYP3A4 substrate + 0.6285 62.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8876 88.76%
CYP3A4 inhibition - 0.5566 55.66%
CYP2C9 inhibition - 0.6925 69.25%
CYP2C19 inhibition - 0.6645 66.45%
CYP2D6 inhibition - 0.8968 89.68%
CYP1A2 inhibition - 0.7192 71.92%
CYP2C8 inhibition - 0.6707 67.07%
CYP inhibitory promiscuity - 0.7682 76.82%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5742 57.42%
Eye corrosion - 0.9843 98.43%
Eye irritation - 0.8831 88.31%
Skin irritation - 0.6402 64.02%
Skin corrosion - 0.9549 95.49%
Ames mutagenesis - 0.6470 64.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7561 75.61%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5906 59.06%
skin sensitisation - 0.8008 80.08%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.5328 53.28%
Acute Oral Toxicity (c) III 0.6277 62.77%
Estrogen receptor binding + 0.6715 67.15%
Androgen receptor binding + 0.6548 65.48%
Thyroid receptor binding + 0.6731 67.31%
Glucocorticoid receptor binding + 0.6938 69.38%
Aromatase binding + 0.5819 58.19%
PPAR gamma + 0.5400 54.00%
Honey bee toxicity - 0.8937 89.37%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9952 99.52%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.52% 97.25%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 94.78% 83.57%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.60% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.26% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.24% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.32% 96.61%
CHEMBL2581 P07339 Cathepsin D 88.56% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.89% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.70% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.25% 86.33%
CHEMBL230 P35354 Cyclooxygenase-2 83.00% 89.63%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.20% 94.80%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.14% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.42% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 81.03% 94.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Hoffmannia strigillosa

Cross-Links

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PubChem 14707560
LOTUS LTS0047845
wikiData Q105254625