Humulane-1,6-dien-3-ol

Details

Top
Internal ID 7cc38438-7e28-4d63-a53b-52b1ea2ce1b5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2Z,8E)-3,7,7,10-tetramethylcycloundeca-2,8-dien-1-ol
SMILES (Canonical) CC1CC(C=C(CCCC(C=C1)(C)C)C)O
SMILES (Isomeric) CC\1CC(/C=C(\CCCC(/C=C1)(C)C)/C)O
InChI InChI=1S/C15H26O/c1-12-6-5-8-15(3,4)9-7-13(2)11-14(16)10-12/h7,9-10,13-14,16H,5-6,8,11H2,1-4H3/b9-7+,12-10-
InChI Key OLKBYNHEDMHHQA-IOIMVZBSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
OLKBYNHEDMHHQA-IOIMVZBSSA-N
3,7,7,10-Tetramethyl-2,8-cycloundecadien-1-ol
3,7,7,10-Tetramethyl-2,8-cycloundecadien-1-ol #

2D Structure

Top
2D Structure of Humulane-1,6-dien-3-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.9287 92.87%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5452 54.52%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.8579 85.79%
OATP1B3 inhibitior + 0.9638 96.38%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.5712 57.12%
P-glycoprotein inhibitior - 0.9392 93.92%
P-glycoprotein substrate - 0.8799 87.99%
CYP3A4 substrate + 0.5468 54.68%
CYP2C9 substrate - 0.6107 61.07%
CYP2D6 substrate - 0.7604 76.04%
CYP3A4 inhibition - 0.9008 90.08%
CYP2C9 inhibition - 0.7922 79.22%
CYP2C19 inhibition - 0.7639 76.39%
CYP2D6 inhibition - 0.9319 93.19%
CYP1A2 inhibition - 0.7386 73.86%
CYP2C8 inhibition - 0.8553 85.53%
CYP inhibitory promiscuity - 0.8760 87.60%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.6037 60.37%
Eye corrosion - 0.9099 90.99%
Eye irritation - 0.7273 72.73%
Skin irritation + 0.8242 82.42%
Skin corrosion - 0.8965 89.65%
Ames mutagenesis - 0.6464 64.64%
Human Ether-a-go-go-Related Gene inhibition - 0.5683 56.83%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5417 54.17%
skin sensitisation + 0.8240 82.40%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.8050 80.50%
Acute Oral Toxicity (c) III 0.8321 83.21%
Estrogen receptor binding - 0.8725 87.25%
Androgen receptor binding - 0.7580 75.80%
Thyroid receptor binding - 0.5291 52.91%
Glucocorticoid receptor binding - 0.7296 72.96%
Aromatase binding - 0.6770 67.70%
PPAR gamma - 0.7453 74.53%
Honey bee toxicity - 0.8865 88.65%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.7505 75.05%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.52% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.94% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.91% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.68% 97.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 87.62% 86.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.31% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.24% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.74% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.16% 92.94%

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.
Conioselinum anthriscoides
Ligusticum officinale

Cross-Links

Top
PubChem 5353015
NPASS NPC213244