Lanopylin B1

Details

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Internal ID c366cf00-57af-401f-99c5-f4b45d008fab
Taxonomy Organoheterocyclic compounds > Pyrrolines
IUPAC Name (4E)-4-heptadecylidene-5-methyl-2,3-dihydropyrrole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H41N/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-22-19-20-23-21(22)2/h18H,3-17,19-20H2,1-2H3/b22-18+
InChI Key YTIMJDBYTSJTGL-RELWKKBWSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C22H41N
Molecular Weight 319.60 g/mol
Exact Mass 319.323900312 g/mol
Topological Polar Surface Area (TPSA) 12.40 Ų
XlogP 8.80
Atomic LogP (AlogP) 7.65
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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(4E)-4-Heptadecylidene-5-methyl-2,3-dihydropyrrole

2D Structure

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2D Structure of Lanopylin B1

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 + 0.8064 80.64%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.4409 44.09%
OATP2B1 inhibitior - 0.8519 85.19%
OATP1B1 inhibitior + 0.9386 93.86%
OATP1B3 inhibitior + 0.9406 94.06%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.8358 83.58%
P-glycoprotein inhibitior - 0.7733 77.33%
P-glycoprotein substrate - 0.8881 88.81%
CYP3A4 substrate - 0.5469 54.69%
CYP2C9 substrate - 0.5986 59.86%
CYP2D6 substrate - 0.8566 85.66%
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 - 0.8047 80.47%
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 + 0.7313 73.13%
Skin irritation - 0.5142 51.42%
Skin corrosion + 0.5426 54.26%
Ames mutagenesis - 0.8537 85.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6811 68.11%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5408 54.08%
skin sensitisation - 0.5950 59.50%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6787 67.87%
Acute Oral Toxicity (c) III 0.5862 58.62%
Estrogen receptor binding - 0.5850 58.50%
Androgen receptor binding - 0.5943 59.43%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.7308 73.08%
Aromatase binding - 0.6015 60.15%
PPAR gamma + 0.5980 59.80%
Honey bee toxicity - 0.9865 98.65%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.8970 89.70%
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 95.82% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 93.58% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.04% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.92% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.18% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.81% 91.81%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.15% 90.08%
CHEMBL240 Q12809 HERG 83.33% 89.76%
CHEMBL2664 P23526 Adenosylhomocysteinase 83.03% 86.67%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.65% 92.86%

Plants that contains it

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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.
There are no matching plants.

Cross-Links

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PubChem 10087332
LOTUS LTS0051207
wikiData Q105361469