15,16-Dihydro-15-methoxy-16-oxohardwickiic acid

Details

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Internal ID 066739a0-a550-4b75-9992-fada6f70f728
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name 5-[2-(2-methoxy-5-oxo-2H-furan-4-yl)ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid
SMILES (Canonical) CC1CCC2(C(C1(C)CCC3=CC(OC3=O)OC)CCC=C2C(=O)O)C
SMILES (Isomeric) CC1CCC2(C(C1(C)CCC3=CC(OC3=O)OC)CCC=C2C(=O)O)C
InChI InChI=1S/C21H30O5/c1-13-8-10-21(3)15(18(22)23)6-5-7-16(21)20(13,2)11-9-14-12-17(25-4)26-19(14)24/h6,12-13,16-17H,5,7-11H2,1-4H3,(H,22,23)
InChI Key LKCDRCCSEGFFNK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H30O5
Molecular Weight 362.50 g/mol
Exact Mass 362.20932405 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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AKOS032948229

2D Structure

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2D Structure of 15,16-Dihydro-15-methoxy-16-oxohardwickiic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9814 98.14%
Caco-2 + 0.6712 67.12%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6614 66.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8550 85.50%
OATP1B3 inhibitior + 0.8497 84.97%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6771 67.71%
BSEP inhibitior + 0.5648 56.48%
P-glycoprotein inhibitior - 0.5473 54.73%
P-glycoprotein substrate - 0.7914 79.14%
CYP3A4 substrate + 0.6389 63.89%
CYP2C9 substrate - 0.8047 80.47%
CYP2D6 substrate - 0.9049 90.49%
CYP3A4 inhibition - 0.7058 70.58%
CYP2C9 inhibition - 0.7529 75.29%
CYP2C19 inhibition - 0.8272 82.72%
CYP2D6 inhibition - 0.9354 93.54%
CYP1A2 inhibition + 0.5604 56.04%
CYP2C8 inhibition + 0.4575 45.75%
CYP inhibitory promiscuity - 0.7644 76.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5787 57.87%
Eye corrosion - 0.9853 98.53%
Eye irritation - 0.9307 93.07%
Skin irritation - 0.5300 53.00%
Skin corrosion - 0.9340 93.40%
Ames mutagenesis - 0.6554 65.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.5495 54.95%
skin sensitisation - 0.8062 80.62%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.5119 51.19%
Acute Oral Toxicity (c) III 0.4220 42.20%
Estrogen receptor binding + 0.8440 84.40%
Androgen receptor binding + 0.5493 54.93%
Thyroid receptor binding + 0.6742 67.42%
Glucocorticoid receptor binding + 0.7529 75.29%
Aromatase binding + 0.7866 78.66%
PPAR gamma + 0.6773 67.73%
Honey bee toxicity - 0.7798 77.98%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.26% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.15% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.46% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.61% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.84% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.81% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.45% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.14% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.73% 94.45%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.90% 93.00%
CHEMBL5028 O14672 ADAM10 81.74% 97.50%

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.
Nanuza plicata
Rydingia limbata

Cross-Links

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PubChem 72834591
LOTUS LTS0189468
wikiData Q105152972