Isoadenolin F

Details

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Internal ID 29df07fb-2ed6-432f-b470-38c240326369
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name [(1S,2S,3S,5S,7R,8R,9S,10S,11R,16S,18R)-3,7,9,18-tetrahydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-10-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H34O8/c1-10-12-9-13(25)14-21-8-6-7-20(3,4)15(21)18(30-11(2)24)23(28,31-19(21)29-5)22(14,16(10)26)17(12)27/h12-19,25-28H,1,6-9H2,2-5H3/t12-,13-,14-,15+,16+,17+,18-,19-,21-,22-,23+/m0/s1
InChI Key LFLIJTKINZDKGG-OZSUYHPESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H34O8
Molecular Weight 438.50 g/mol
Exact Mass 438.22536804 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.71
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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CHEMBL1802171

2D Structure

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2D Structure of Isoadenolin F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9455 94.55%
Caco-2 - 0.7767 77.67%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5795 57.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8132 81.32%
OATP1B3 inhibitior + 0.8443 84.43%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7321 73.21%
BSEP inhibitior - 0.8839 88.39%
P-glycoprotein inhibitior - 0.6864 68.64%
P-glycoprotein substrate - 0.5833 58.33%
CYP3A4 substrate + 0.6898 68.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8643 86.43%
CYP3A4 inhibition - 0.6782 67.82%
CYP2C9 inhibition - 0.6774 67.74%
CYP2C19 inhibition - 0.6944 69.44%
CYP2D6 inhibition - 0.9125 91.25%
CYP1A2 inhibition - 0.7304 73.04%
CYP2C8 inhibition + 0.5542 55.42%
CYP inhibitory promiscuity - 0.9005 90.05%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6647 66.47%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.9134 91.34%
Skin irritation - 0.5456 54.56%
Skin corrosion - 0.9157 91.57%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6261 62.61%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5358 53.58%
skin sensitisation - 0.7901 79.01%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.6013 60.13%
Acute Oral Toxicity (c) I 0.3533 35.33%
Estrogen receptor binding + 0.7659 76.59%
Androgen receptor binding + 0.6977 69.77%
Thyroid receptor binding + 0.5493 54.93%
Glucocorticoid receptor binding + 0.5891 58.91%
Aromatase binding + 0.6196 61.96%
PPAR gamma + 0.6164 61.64%
Honey bee toxicity - 0.7160 71.60%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9551 95.51%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.29% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.07% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 90.91% 97.79%
CHEMBL2581 P07339 Cathepsin D 89.84% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 88.96% 91.19%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.84% 91.07%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.83% 95.50%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.82% 91.24%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 86.20% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.74% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.73% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.56% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.55% 97.25%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.42% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.91% 97.09%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.89% 97.28%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.88% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.85% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.66% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.85% 85.14%

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.
Isodon adenolomus

Cross-Links

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PubChem 56673382
LOTUS LTS0149850
wikiData Q105151062