Kauren-19-ol

Details

Top
Internal ID 699075da-6ef5-42cb-8878-bc440c508b64
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name (5,9,14-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methanol
SMILES (Canonical) CC1CC23CCC4C(CCCC4(C2CCC1C3)C)(C)CO
SMILES (Isomeric) CC1CC23CCC4C(CCCC4(C2CCC1C3)C)(C)CO
InChI InChI=1S/C20H34O/c1-14-11-20-10-7-16-18(2,13-21)8-4-9-19(16,3)17(20)6-5-15(14)12-20/h14-17,21H,4-13H2,1-3H3
InChI Key YNHXWZNOUUQLCY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H34O
Molecular Weight 290.50 g/mol
Exact Mass 290.260965704 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.03
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
YNHXWZNOUUQLCY-UHFFFAOYSA-N

2D Structure

Top
2D Structure of Kauren-19-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.7413 74.13%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.8048 80.48%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.8832 88.32%
OATP1B3 inhibitior + 0.8860 88.60%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6942 69.42%
P-glycoprotein inhibitior - 0.8354 83.54%
P-glycoprotein substrate - 0.8293 82.93%
CYP3A4 substrate + 0.5934 59.34%
CYP2C9 substrate - 0.6107 61.07%
CYP2D6 substrate - 0.7282 72.82%
CYP3A4 inhibition - 0.8167 81.67%
CYP2C9 inhibition + 0.5979 59.79%
CYP2C19 inhibition - 0.6201 62.01%
CYP2D6 inhibition - 0.9039 90.39%
CYP1A2 inhibition - 0.6557 65.57%
CYP2C8 inhibition - 0.7234 72.34%
CYP inhibitory promiscuity - 0.7845 78.45%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6619 66.19%
Eye corrosion - 0.9284 92.84%
Eye irritation - 0.6787 67.87%
Skin irritation - 0.8507 85.07%
Skin corrosion - 0.9697 96.97%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5699 56.99%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6601 66.01%
skin sensitisation + 0.5164 51.64%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.8551 85.51%
Acute Oral Toxicity (c) III 0.7534 75.34%
Estrogen receptor binding + 0.7806 78.06%
Androgen receptor binding - 0.5474 54.74%
Thyroid receptor binding + 0.6543 65.43%
Glucocorticoid receptor binding + 0.5624 56.24%
Aromatase binding + 0.5240 52.40%
PPAR gamma - 0.7324 73.24%
Honey bee toxicity - 0.8922 89.22%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9728 97.28%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.97% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.95% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 90.40% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.29% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.13% 91.11%
CHEMBL237 P41145 Kappa opioid receptor 89.11% 98.10%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 88.38% 95.50%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.71% 82.69%
CHEMBL206 P03372 Estrogen receptor alpha 82.44% 97.64%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.21% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 81.90% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.88% 95.89%
CHEMBL259 P32245 Melanocortin receptor 4 80.70% 95.38%
CHEMBL3012 Q13946 Phosphodiesterase 7A 80.49% 99.29%

Plants that contains it

Top
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.
Disynaphia multicrenulata
Helichrysum aureum

Cross-Links

Top
PubChem 530420
LOTUS LTS0178280
wikiData Q104396568