Penicillar D

Details

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Internal ID 2dec36ff-8850-4c72-b806-34a11851e4c5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > C-glycosyl compounds
IUPAC Name (2R,3R,5R)-2-[(1E)-buta-1,3-dienyl]-5-methyloxolan-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H14O2/c1-3-4-5-9-8(10)6-7(2)11-9/h3-5,7-10H,1,6H2,2H3/b5-4+/t7-,8-,9-/m1/s1
InChI Key GUXAFFOQBHDGJZ-VARVQHAUSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O2
Molecular Weight 154.21 g/mol
Exact Mass 154.099379685 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.27
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Penicillar D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9896 98.96%
Caco-2 + 0.6900 69.00%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.4052 40.52%
OATP2B1 inhibitior - 0.8640 86.40%
OATP1B1 inhibitior + 0.9287 92.87%
OATP1B3 inhibitior + 0.9626 96.26%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9574 95.74%
P-glycoprotein inhibitior - 0.9811 98.11%
P-glycoprotein substrate - 0.9323 93.23%
CYP3A4 substrate - 0.5577 55.77%
CYP2C9 substrate - 0.8047 80.47%
CYP2D6 substrate - 0.7647 76.47%
CYP3A4 inhibition - 0.9769 97.69%
CYP2C9 inhibition - 0.9660 96.60%
CYP2C19 inhibition - 0.8504 85.04%
CYP2D6 inhibition - 0.9585 95.85%
CYP1A2 inhibition - 0.7630 76.30%
CYP2C8 inhibition - 0.9656 96.56%
CYP inhibitory promiscuity - 0.8819 88.19%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8435 84.35%
Carcinogenicity (trinary) Non-required 0.4220 42.20%
Eye corrosion - 0.5942 59.42%
Eye irritation - 0.5752 57.52%
Skin irritation + 0.6132 61.32%
Skin corrosion - 0.6442 64.42%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6929 69.29%
Micronuclear - 0.7068 70.68%
Hepatotoxicity + 0.7073 70.73%
skin sensitisation + 0.5407 54.07%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6023 60.23%
Estrogen receptor binding - 0.8817 88.17%
Androgen receptor binding - 0.9148 91.48%
Thyroid receptor binding - 0.6874 68.74%
Glucocorticoid receptor binding - 0.7829 78.29%
Aromatase binding - 0.8690 86.90%
PPAR gamma - 0.6416 64.16%
Honey bee toxicity - 0.6261 62.61%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.6854 68.54%

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
CHEMBL226 P30542 Adenosine A1 receptor 88.69% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.42% 96.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 85.09% 95.58%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.00% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.60% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.68% 89.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139588226
LOTUS LTS0250529
wikiData Q105107413