Peniciaculin B

Details

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Internal ID 47b7a5b8-08f8-4432-b819-20b8150d65bd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [3-hydroxy-4-[(2S)-2-hydroxy-6-methylheptan-2-yl]phenyl]methyl 3-hydroxy-4-[(2S)-2-hydroxy-6-methylheptan-2-yl]benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H44O6/c1-20(2)9-7-15-29(5,34)24-13-11-22(17-26(24)31)19-36-28(33)23-12-14-25(27(32)18-23)30(6,35)16-8-10-21(3)4/h11-14,17-18,20-21,31-32,34-35H,7-10,15-16,19H2,1-6H3/t29-,30-/m0/s1
InChI Key KNIRNRYVMBOJSZ-KYJUHHDHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H44O6
Molecular Weight 500.70 g/mol
Exact Mass 500.31378912 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 7.50
Atomic LogP (AlogP) 6.52
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 13

Synonyms

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(3-hydroxy-4-((2S)-2-hydroxy-6-methylheptan-2-yl)phenyl)methyl 3-hydroxy-4-((2S)-2-hydroxy-6-methylheptan-2-yl)benzoate
[3-hydroxy-4-[(2S)-2-hydroxy-6-methylheptan-2-yl]phenyl]methyl 3-hydroxy-4-[(2S)-2-hydroxy-6-methylheptan-2-yl]benzoate
RefChem:170820
CHEMBL3577361
CHEBI:220177

2D Structure

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2D Structure of Peniciaculin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9738 97.38%
Caco-2 - 0.7153 71.53%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.9008 90.08%
OATP2B1 inhibitior - 0.7145 71.45%
OATP1B1 inhibitior + 0.9135 91.35%
OATP1B3 inhibitior + 0.8847 88.47%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9143 91.43%
P-glycoprotein inhibitior + 0.7649 76.49%
P-glycoprotein substrate - 0.5784 57.84%
CYP3A4 substrate + 0.5339 53.39%
CYP2C9 substrate - 0.5973 59.73%
CYP2D6 substrate - 0.8202 82.02%
CYP3A4 inhibition - 0.7922 79.22%
CYP2C9 inhibition + 0.7526 75.26%
CYP2C19 inhibition - 0.8199 81.99%
CYP2D6 inhibition - 0.9271 92.71%
CYP1A2 inhibition + 0.7175 71.75%
CYP2C8 inhibition + 0.6047 60.47%
CYP inhibitory promiscuity - 0.7583 75.83%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6119 61.19%
Eye corrosion - 0.9945 99.45%
Eye irritation - 0.8467 84.67%
Skin irritation - 0.7662 76.62%
Skin corrosion - 0.9584 95.84%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4799 47.99%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8063 80.63%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.8729 87.29%
Acute Oral Toxicity (c) III 0.7451 74.51%
Estrogen receptor binding + 0.7221 72.21%
Androgen receptor binding + 0.8225 82.25%
Thyroid receptor binding + 0.6842 68.42%
Glucocorticoid receptor binding + 0.6680 66.80%
Aromatase binding + 0.6164 61.64%
PPAR gamma + 0.6854 68.54%
Honey bee toxicity - 0.8737 87.37%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9920 99.20%

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
CHEMBL2179 P04062 Beta-glucocerebrosidase 99.08% 85.31%
CHEMBL2581 P07339 Cathepsin D 98.43% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.72% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 93.89% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.68% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.17% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 91.05% 94.73%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 90.53% 85.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.27% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.13% 90.71%
CHEMBL1951 P21397 Monoamine oxidase A 87.63% 91.49%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.40% 95.89%
CHEMBL2535 P11166 Glucose transporter 86.21% 98.75%
CHEMBL1907588 P02708 Acetylcholine receptor; alpha1/beta1/delta/gamma 85.89% 98.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.03% 96.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.00% 97.29%
CHEMBL236 P41143 Delta opioid receptor 83.46% 99.35%
CHEMBL3524 P56524 Histone deacetylase 4 83.46% 92.97%
CHEMBL3194 P02766 Transthyretin 82.56% 90.71%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.53% 97.21%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.38% 94.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.00% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.07% 95.56%
CHEMBL2039 P27338 Monoamine oxidase B 80.84% 92.51%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.24% 94.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.06% 93.56%

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 122177658
LOTUS LTS0158733
wikiData Q77504223