(+)-alpha-Pinguisene

Details

Top
Internal ID 722ffc43-c0f6-4767-bedf-0fd8732325ba
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,3aS,4R,7aS)-5-ethenyl-1,3a,4,7a-tetramethyl-2,3,4,7-tetrahydro-1H-indene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-6-13-8-10-14(4)11(2)7-9-15(14,5)12(13)3/h6,8,11-12H,1,7,9-10H2,2-5H3/t11-,12-,14+,15+/m1/s1
InChI Key PFLVCUHFTYXGSL-UXOAXIEHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
LMPR0103520001
(1R,3aS,4R,7aS)-5-ethenyl-1,3a,4,7a-tetramethyl-2,3,4,7-tetrahydro-1H-indene

2D Structure

Top
2D Structure of (+)-alpha-Pinguisene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.8384 83.84%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.8176 81.76%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9335 93.35%
OATP1B3 inhibitior + 0.8528 85.28%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9417 94.17%
P-glycoprotein inhibitior - 0.9389 93.89%
P-glycoprotein substrate - 0.8476 84.76%
CYP3A4 substrate - 0.5166 51.66%
CYP2C9 substrate - 0.7985 79.85%
CYP2D6 substrate - 0.7625 76.25%
CYP3A4 inhibition - 0.8028 80.28%
CYP2C9 inhibition - 0.8184 81.84%
CYP2C19 inhibition - 0.7452 74.52%
CYP2D6 inhibition - 0.9449 94.49%
CYP1A2 inhibition - 0.7462 74.62%
CYP2C8 inhibition - 0.8195 81.95%
CYP inhibitory promiscuity - 0.6671 66.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Warning 0.4713 47.13%
Eye corrosion - 0.9345 93.45%
Eye irritation + 0.5621 56.21%
Skin irritation + 0.5285 52.85%
Skin corrosion - 0.9808 98.08%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5320 53.20%
skin sensitisation + 0.8485 84.85%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7281 72.81%
Acute Oral Toxicity (c) III 0.7465 74.65%
Estrogen receptor binding - 0.8329 83.29%
Androgen receptor binding - 0.5844 58.44%
Thyroid receptor binding - 0.7794 77.94%
Glucocorticoid receptor binding - 0.9001 90.01%
Aromatase binding - 0.7506 75.06%
PPAR gamma - 0.8316 83.16%
Honey bee toxicity - 0.8364 83.64%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 1.0000 100.00%

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 95.70% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.61% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.34% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.05% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.89% 97.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 89.37% 86.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.95% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.19% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.09% 95.56%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.35% 90.24%
CHEMBL1937 Q92769 Histone deacetylase 2 81.51% 94.75%

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.
Porella canariensis
Porella vernicosa

Cross-Links

Top
PubChem 10104368
LOTUS LTS0136018
wikiData Q76415121