Lanopylin A2

Details

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Internal ID e2580a72-34b5-4951-bf63-e9d98de80b13
Taxonomy Organoheterocyclic compounds > Pyrrolines
IUPAC Name (4E)-5-methyl-4-[(Z)-17-methyloctadec-12-enylidene]-2,3-dihydropyrrole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H43N/c1-22(2)18-16-14-12-10-8-6-4-5-7-9-11-13-15-17-19-24-20-21-25-23(24)3/h10,12,19,22H,4-9,11,13-18,20-21H2,1-3H3/b12-10-,24-19+
InChI Key SHGBXBWAMDQWFA-XKZRXXLSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H43N
Molecular Weight 345.60 g/mol
Exact Mass 345.339550376 g/mol
Topological Polar Surface Area (TPSA) 12.40 Ų
XlogP 8.70
Atomic LogP (AlogP) 8.06
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Lanopylin A2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9858 98.58%
Caco-2 + 0.6343 63.43%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.3680 36.80%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9402 94.02%
OATP1B3 inhibitior + 0.9323 93.23%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior + 0.8695 86.95%
P-glycoprotein inhibitior - 0.6365 63.65%
P-glycoprotein substrate - 0.7794 77.94%
CYP3A4 substrate + 0.5220 52.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8622 86.22%
CYP3A4 inhibition - 0.9575 95.75%
CYP2C9 inhibition - 0.8141 81.41%
CYP2C19 inhibition - 0.7500 75.00%
CYP2D6 inhibition - 0.7454 74.54%
CYP1A2 inhibition - 0.5739 57.39%
CYP2C8 inhibition - 0.9119 91.19%
CYP inhibitory promiscuity - 0.7825 78.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5445 54.45%
Eye corrosion - 0.8035 80.35%
Eye irritation - 0.6265 62.65%
Skin irritation + 0.5079 50.79%
Skin corrosion + 0.6153 61.53%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7725 77.25%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.5842 58.42%
skin sensitisation - 0.5776 57.76%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8305 83.05%
Acute Oral Toxicity (c) III 0.6397 63.97%
Estrogen receptor binding - 0.6039 60.39%
Androgen receptor binding - 0.6337 63.37%
Thyroid receptor binding + 0.6695 66.95%
Glucocorticoid receptor binding - 0.4838 48.38%
Aromatase binding - 0.6608 66.08%
PPAR gamma + 0.7295 72.95%
Honey bee toxicity - 0.9612 96.12%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9559 95.59%

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
CHEMBL2581 P07339 Cathepsin D 95.43% 98.95%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 94.26% 92.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.29% 99.17%
CHEMBL5103 Q969S8 Histone deacetylase 10 90.71% 90.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.24% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.46% 93.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.24% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 83.32% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.15% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.90% 93.99%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.72% 98.33%
CHEMBL1937 Q92769 Histone deacetylase 2 80.94% 94.75%
CHEMBL4302 P08183 P-glycoprotein 1 80.72% 92.98%
CHEMBL1907 P15144 Aminopeptidase N 80.30% 93.31%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.21% 96.47%

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 11427950
LOTUS LTS0205587
wikiData Q77495467