11beta-Hydroxykaur-16-en-15-one

Details

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Internal ID bc749b0d-6199-46b7-92e1-d6bee6d42ce1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name (1R,4R,9R,10S,11S,13S)-11-hydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one
SMILES (Canonical) CC1(CCCC2(C1CCC34C2C(CC(C3)C(=C)C4=O)O)C)C
SMILES (Isomeric) C[C@@]12CCCC([C@H]1CC[C@]34[C@H]2[C@H](C[C@H](C3)C(=C)C4=O)O)(C)C
InChI InChI=1S/C20H30O2/c1-12-13-10-14(21)16-19(4)8-5-7-18(2,3)15(19)6-9-20(16,11-13)17(12)22/h13-16,21H,1,5-11H2,2-4H3/t13-,14+,15-,16+,19-,20-/m1/s1
InChI Key CNFJKVOXPKJCBT-SPBSJPQISA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H30O2
Molecular Weight 302.50 g/mol
Exact Mass 302.224580195 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.13
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 11beta-Hydroxykaur-16-en-15-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.7137 71.37%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.5652 56.52%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.8305 83.05%
OATP1B3 inhibitior + 0.8432 84.32%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior - 0.6877 68.77%
P-glycoprotein inhibitior - 0.7984 79.84%
P-glycoprotein substrate - 0.8769 87.69%
CYP3A4 substrate + 0.6528 65.28%
CYP2C9 substrate - 0.7954 79.54%
CYP2D6 substrate - 0.7970 79.70%
CYP3A4 inhibition - 0.8670 86.70%
CYP2C9 inhibition - 0.8279 82.79%
CYP2C19 inhibition - 0.7029 70.29%
CYP2D6 inhibition - 0.9479 94.79%
CYP1A2 inhibition - 0.7880 78.80%
CYP2C8 inhibition - 0.7814 78.14%
CYP inhibitory promiscuity - 0.8554 85.54%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5711 57.11%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.8177 81.77%
Skin irritation + 0.6639 66.39%
Skin corrosion - 0.9591 95.91%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7577 75.77%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5931 59.31%
skin sensitisation + 0.5189 51.89%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.7118 71.18%
Acute Oral Toxicity (c) III 0.7888 78.88%
Estrogen receptor binding + 0.8186 81.86%
Androgen receptor binding + 0.6321 63.21%
Thyroid receptor binding + 0.6343 63.43%
Glucocorticoid receptor binding + 0.8476 84.76%
Aromatase binding + 0.6196 61.96%
PPAR gamma - 0.5717 57.17%
Honey bee toxicity - 0.8225 82.25%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9937 99.37%

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
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 94.17% 82.69%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.58% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.02% 91.11%
CHEMBL1902 P62942 FK506-binding protein 1A 91.64% 97.05%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 90.59% 96.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.46% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 87.05% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.64% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.62% 96.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.47% 93.04%
CHEMBL1871 P10275 Androgen Receptor 86.47% 96.43%
CHEMBL2581 P07339 Cathepsin D 85.94% 98.95%
CHEMBL259 P32245 Melanocortin receptor 4 85.90% 95.38%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.46% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.72% 94.45%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.53% 93.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.31% 95.89%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.21% 90.08%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.83% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.40% 99.23%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 80.97% 100.00%

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.
Jackiella javanica
Jungermannia exsertifolia
Jungermannia infusca
Jungermannia truncata
Liochlaena subulata

Cross-Links

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PubChem 101831563
LOTUS LTS0041663
wikiData Q104965716