(2R)-pterosin P

Details

Top
Internal ID eeeabcb7-a481-44be-9644-caebce631df2
Taxonomy Benzenoids > Indanes > Indanones
IUPAC Name (2R)-6-(2-hydroxyethyl)-5-(hydroxymethyl)-2,7-dimethyl-2,3-dihydroinden-1-one
SMILES (Canonical) CC1CC2=CC(=C(C(=C2C1=O)C)CCO)CO
SMILES (Isomeric) C[C@@H]1CC2=CC(=C(C(=C2C1=O)C)CCO)CO
InChI InChI=1S/C14H18O3/c1-8-5-10-6-11(7-16)12(3-4-15)9(2)13(10)14(8)17/h6,8,15-16H,3-5,7H2,1-2H3/t8-/m1/s1
InChI Key QDZJDGJEGHSXFF-MRVPVSSYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H18O3
Molecular Weight 234.29 g/mol
Exact Mass 234.125594432 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.40
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
CHEBI:69468
Q27137806

2D Structure

Top
2D Structure of (2R)-pterosin P

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.7853 78.53%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7938 79.38%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.8733 87.33%
OATP1B3 inhibitior + 0.9504 95.04%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.8088 80.88%
P-glycoprotein inhibitior - 0.9409 94.09%
P-glycoprotein substrate - 0.7928 79.28%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8047 80.47%
CYP3A4 inhibition - 0.7694 76.94%
CYP2C9 inhibition - 0.8438 84.38%
CYP2C19 inhibition - 0.8181 81.81%
CYP2D6 inhibition - 0.8966 89.66%
CYP1A2 inhibition + 0.5779 57.79%
CYP2C8 inhibition - 0.9457 94.57%
CYP inhibitory promiscuity - 0.8835 88.35%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.7078 70.78%
Eye corrosion - 0.9902 99.02%
Eye irritation + 0.7004 70.04%
Skin irritation - 0.6771 67.71%
Skin corrosion - 0.9614 96.14%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6508 65.08%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.7026 70.26%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7252 72.52%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8442 84.42%
Acute Oral Toxicity (c) III 0.6986 69.86%
Estrogen receptor binding - 0.8074 80.74%
Androgen receptor binding - 0.4841 48.41%
Thyroid receptor binding - 0.6547 65.47%
Glucocorticoid receptor binding - 0.6282 62.82%
Aromatase binding - 0.8476 84.76%
PPAR gamma - 0.7414 74.14%
Honey bee toxicity - 0.9353 93.53%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9434 94.34%

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
CHEMBL2581 P07339 Cathepsin D 96.17% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.86% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.38% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.19% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 86.76% 86.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.58% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.98% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.46% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.00% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.42% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.28% 90.71%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.70% 96.25%
CHEMBL4208 P20618 Proteasome component C5 81.65% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 81.43% 94.73%

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.
Acrostichum aureum
Anthocleista procera
Crepidiastrum denticulatum subsp. denticulatum
Pseudognaphalium oligandrum
Sideritis hirsuta
Wulfenia orientalis

Cross-Links

Top
PubChem 70698132
NPASS NPC183211
LOTUS LTS0092002
wikiData Q27137806