1(10)E,5E-germacradiene-3,11-diol

Details

Top
Internal ID 5099f448-3fbb-4a42-8264-f0cb2828b3f2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name (1R,2R,3Z,5R,8Z)-5-(2-hydroxypropan-2-yl)-2,8-dimethylcyclodeca-3,8-dien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O2/c1-11-5-8-13(15(3,4)17)9-7-12(2)14(16)10-6-11/h6-7,9,12-14,16-17H,5,8,10H2,1-4H3/b9-7-,11-6-/t12-,13-,14-/m1/s1
InChI Key RBBWQOZTCXYKSH-NXIGSEQPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1(10)E,5E-germacradiene-3,11-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.7851 78.51%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.5810 58.10%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9430 94.30%
OATP1B3 inhibitior + 0.9681 96.81%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7593 75.93%
P-glycoprotein inhibitior - 0.9339 93.39%
P-glycoprotein substrate - 0.7856 78.56%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7880 78.80%
CYP2D6 substrate - 0.7641 76.41%
CYP3A4 inhibition - 0.7909 79.09%
CYP2C9 inhibition - 0.8589 85.89%
CYP2C19 inhibition - 0.7880 78.80%
CYP2D6 inhibition - 0.9377 93.77%
CYP1A2 inhibition - 0.7106 71.06%
CYP2C8 inhibition - 0.8471 84.71%
CYP inhibitory promiscuity - 0.8095 80.95%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.6088 60.88%
Eye corrosion - 0.9656 96.56%
Eye irritation - 0.8281 82.81%
Skin irritation + 0.6099 60.99%
Skin corrosion - 0.9638 96.38%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5297 52.97%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5821 58.21%
skin sensitisation + 0.7177 71.77%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.8216 82.16%
Acute Oral Toxicity (c) III 0.7722 77.22%
Estrogen receptor binding - 0.8212 82.12%
Androgen receptor binding - 0.8219 82.19%
Thyroid receptor binding - 0.5305 53.05%
Glucocorticoid receptor binding - 0.4705 47.05%
Aromatase binding - 0.8319 83.19%
PPAR gamma - 0.7727 77.27%
Honey bee toxicity - 0.9393 93.93%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9417 94.17%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.83% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.79% 97.25%
CHEMBL2581 P07339 Cathepsin D 85.61% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.74% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 83.65% 94.73%
CHEMBL1871 P10275 Androgen Receptor 82.72% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.10% 95.89%

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.
There are no matching plants.

Cross-Links

Top
PubChem 139586803
LOTUS LTS0206983
wikiData Q77514924