Piptamine

Details

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Internal ID 47750d60-608d-4a43-adb8-229323b80e6b
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylmethylamines
IUPAC Name N-benzyl-N-methylpentadecan-1-amine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H41N/c1-3-4-5-6-7-8-9-10-11-12-13-14-18-21-24(2)22-23-19-16-15-17-20-23/h15-17,19-20H,3-14,18,21-22H2,1-2H3
InChI Key YMMNFUJNCOWQRX-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C23H41N
Molecular Weight 331.60 g/mol
Exact Mass 331.323900312 g/mol
Topological Polar Surface Area (TPSA) 3.20 Ų
XlogP 9.00
Atomic LogP (AlogP) 7.21
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

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N-benzyl-N-methylpentadecan-1-amine
Piptamine
SCHEMBL15966133
CHEBI:66758
Q27135385

2D Structure

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2D Structure of Piptamine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9714 97.14%
Caco-2 + 0.7458 74.58%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.7110 71.10%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.8940 89.40%
OATP1B3 inhibitior + 0.9484 94.84%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.5986 59.86%
P-glycoprotein inhibitior - 0.7446 74.46%
P-glycoprotein substrate - 0.7129 71.29%
CYP3A4 substrate - 0.5599 55.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.7494 74.94%
CYP3A4 inhibition - 0.9658 96.58%
CYP2C9 inhibition - 0.9685 96.85%
CYP2C19 inhibition - 0.8540 85.40%
CYP2D6 inhibition + 0.5521 55.21%
CYP1A2 inhibition - 0.6064 60.64%
CYP2C8 inhibition - 0.8821 88.21%
CYP inhibitory promiscuity - 0.9275 92.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6924 69.24%
Eye corrosion + 0.5054 50.54%
Eye irritation - 0.6248 62.48%
Skin irritation + 0.7303 73.03%
Skin corrosion + 0.8912 89.12%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8578 85.78%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.7419 74.19%
skin sensitisation - 0.8349 83.49%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.5321 53.21%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.7438 74.38%
Acute Oral Toxicity (c) II 0.7373 73.73%
Estrogen receptor binding + 0.6874 68.74%
Androgen receptor binding - 0.8057 80.57%
Thyroid receptor binding + 0.6457 64.57%
Glucocorticoid receptor binding - 0.7892 78.92%
Aromatase binding - 0.5996 59.96%
PPAR gamma + 0.5713 57.13%
Honey bee toxicity - 0.9815 98.15%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.8600 86.00%
Fish aquatic toxicity + 0.9218 92.18%

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 98.72% 98.95%
CHEMBL240 Q12809 HERG 94.64% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.02% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.80% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 92.95% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.27% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 86.28% 87.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.19% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.18% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.55% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 83.93% 93.31%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.88% 93.81%
CHEMBL1781 P11387 DNA topoisomerase I 82.82% 97.00%

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 10664275
LOTUS LTS0049039
wikiData Q27135385