Humulenol II

Details

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Internal ID e6865721-6845-454f-baad-0f9b2a2f72fc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4Z,8Z)-6,6,9-trimethyl-2-methylidenecycloundeca-4,8-dien-1-ol
SMILES (Canonical) CC1=CCC(C=CCC(=C)C(CC1)O)(C)C
SMILES (Isomeric) C/C/1=C/CC(/C=C\CC(=C)C(CC1)O)(C)C
InChI InChI=1S/C15H24O/c1-12-7-8-14(16)13(2)6-5-10-15(3,4)11-9-12/h5,9-10,14,16H,2,6-8,11H2,1,3-4H3/b10-5-,12-9-
InChI Key ZHCPVYWHSOILQL-CGBKSYCJSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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RefChem:1086732
(4Z,8Z)-6,6,9-TRIMETHYL-2-METHYLIDENECYCLOUNDECA-4,8-DIEN-1-OL
(+)-Humulenol II

2D Structure

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2D Structure of Humulenol II

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8253 82.53%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4482 44.82%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.9433 94.33%
OATP1B3 inhibitior + 0.8116 81.16%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8718 87.18%
P-glycoprotein inhibitior - 0.9368 93.68%
P-glycoprotein substrate - 0.8591 85.91%
CYP3A4 substrate + 0.5643 56.43%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.8195 81.95%
CYP2C9 inhibition - 0.8421 84.21%
CYP2C19 inhibition - 0.8499 84.99%
CYP2D6 inhibition - 0.9464 94.64%
CYP1A2 inhibition - 0.7913 79.13%
CYP2C8 inhibition - 0.8259 82.59%
CYP inhibitory promiscuity - 0.9081 90.81%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.6198 61.98%
Eye corrosion - 0.9383 93.83%
Eye irritation - 0.6087 60.87%
Skin irritation + 0.7198 71.98%
Skin corrosion - 0.9556 95.56%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7214 72.14%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.7912 79.12%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5149 51.49%
Acute Oral Toxicity (c) III 0.5939 59.39%
Estrogen receptor binding - 0.8380 83.80%
Androgen receptor binding - 0.8231 82.31%
Thyroid receptor binding - 0.6333 63.33%
Glucocorticoid receptor binding - 0.5852 58.52%
Aromatase binding - 0.6319 63.19%
PPAR gamma - 0.6337 63.37%
Honey bee toxicity - 0.9347 93.47%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9725 97.25%

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 93.31% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.54% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.76% 100.00%
CHEMBL1871 P10275 Androgen Receptor 86.72% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.47% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.57% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.55% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.43% 95.89%

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.
Humulus lupulus
Zingiber zerumbet

Cross-Links

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PubChem 102115341
LOTUS LTS0120166
wikiData Q104391247