Lanopylin B2

Details

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Internal ID 6c5490c3-2892-4a7b-9f7d-fe9a348ffbe7
Taxonomy Organoheterocyclic compounds > Pyrrolines
IUPAC Name (4E)-5-methyl-4-[(Z)-nonadec-12-enylidene]-2,3-dihydropyrrole
SMILES (Canonical) CCCCCCC=CCCCCCCCCCCC=C1CCN=C1C
SMILES (Isomeric) CCCCCC/C=C\CCCCCCCCCC/C=C/1\CCN=C1C
InChI InChI=1S/C24H43N/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-24-21-22-25-23(24)2/h8-9,20H,3-7,10-19,21-22H2,1-2H3/b9-8-,24-20+
InChI Key CTEOHBYQNVFMJZ-ZIKBOSLESA-N
Popularity 1 reference 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 9.00
Atomic LogP (AlogP) 8.21
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

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(4E)-5-methyl-4-[(Z)-nonadec-12-enylidene]-2,3-dihydropyrrole
679411-86-0
(4E)-5-methyl-4-((Z)-nonadec-12-enylidene)-2,3-dihydropyrrole
RefChem:152268
orb3024578
CHEBI:204498
HY-N14744

2D Structure

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2D Structure of Lanopylin B2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.6089 60.89%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.4409 44.09%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.9003 90.03%
OATP1B3 inhibitior + 0.9406 94.06%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.8169 81.69%
P-glycoprotein inhibitior - 0.6371 63.71%
P-glycoprotein substrate - 0.8639 86.39%
CYP3A4 substrate - 0.5105 51.05%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8530 85.30%
CYP3A4 inhibition - 0.9501 95.01%
CYP2C9 inhibition - 0.8034 80.34%
CYP2C19 inhibition - 0.7130 71.30%
CYP2D6 inhibition - 0.6984 69.84%
CYP1A2 inhibition + 0.5607 56.07%
CYP2C8 inhibition - 0.7741 77.41%
CYP inhibitory promiscuity - 0.6411 64.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5655 56.55%
Eye corrosion - 0.7269 72.69%
Eye irritation + 0.5936 59.36%
Skin irritation - 0.5142 51.42%
Skin corrosion + 0.5426 54.26%
Ames mutagenesis - 0.7837 78.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7289 72.89%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5342 53.42%
skin sensitisation - 0.5950 59.50%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7257 72.57%
Acute Oral Toxicity (c) III 0.5862 58.62%
Estrogen receptor binding + 0.5575 55.75%
Androgen receptor binding - 0.5501 55.01%
Thyroid receptor binding + 0.5523 55.23%
Glucocorticoid receptor binding - 0.6266 62.66%
Aromatase binding - 0.6006 60.06%
PPAR gamma + 0.6851 68.51%
Honey bee toxicity - 0.9832 98.32%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.9253 92.53%
Fish aquatic toxicity + 0.9638 96.38%

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 95.46% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.06% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 94.02% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.04% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.18% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.97% 91.81%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.87% 90.08%
CHEMBL2664 P23526 Adenosylhomocysteinase 83.03% 86.67%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.60% 100.00%
CHEMBL1781 P11387 DNA topoisomerase I 81.32% 97.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.84% 92.86%

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 11279421
LOTUS LTS0211319
wikiData Q77386228