Tribenzylamine

Details

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Internal ID 66ce7bdc-5045-4e45-a54d-5a216e5c4c3c
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylmethylamines
IUPAC Name N,N-dibenzyl-1-phenylmethanamine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H21N/c1-4-10-19(11-5-1)16-22(17-20-12-6-2-7-13-20)18-21-14-8-3-9-15-21/h1-15H,16-18H2
InChI Key MXHTZQSKTCCMFG-UHFFFAOYSA-N
Popularity 322 references in papers

Physical and Chemical Properties

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Molecular Formula C21H21N
Molecular Weight 287.40 g/mol
Exact Mass 287.167399674 g/mol
Topological Polar Surface Area (TPSA) 3.20 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.89
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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620-40-6
N,N-dibenzyl-1-phenylmethanamine
Benzenemethanamine, N,N-bis(phenylmethyl)-
DTXSID5047031
HZ10O1931J
DTXCID3027031
RefChem:190887
210-638-3
MFCD00004773
N,N-Bis(phenylmethyl)benzenemethanamine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Tribenzylamine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9440 94.40%
Caco-2 + 0.9607 96.07%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.5068 50.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9522 95.22%
OATP1B3 inhibitior + 0.9499 94.99%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior + 0.5879 58.79%
P-glycoprotein inhibitior - 0.9472 94.72%
P-glycoprotein substrate - 0.9722 97.22%
CYP3A4 substrate - 0.7813 78.13%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.7019 70.19%
CYP3A4 inhibition - 0.8879 88.79%
CYP2C9 inhibition - 0.8256 82.56%
CYP2C19 inhibition + 0.7525 75.25%
CYP2D6 inhibition - 0.7268 72.68%
CYP1A2 inhibition + 0.5818 58.18%
CYP2C8 inhibition - 0.9038 90.38%
CYP inhibitory promiscuity + 0.8125 81.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.5136 51.36%
Eye corrosion + 0.7542 75.42%
Eye irritation + 0.9775 97.75%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.6262 62.62%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5067 50.67%
Micronuclear - 0.7232 72.32%
Hepatotoxicity + 0.5483 54.83%
skin sensitisation + 0.5409 54.09%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6032 60.32%
Acute Oral Toxicity (c) III 0.6644 66.44%
Estrogen receptor binding + 0.5591 55.91%
Androgen receptor binding - 0.7977 79.77%
Thyroid receptor binding - 0.6129 61.29%
Glucocorticoid receptor binding - 0.7861 78.61%
Aromatase binding + 0.8113 81.13%
PPAR gamma + 0.8161 81.61%
Honey bee toxicity - 0.9293 92.93%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.8550 85.50%

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
CHEMBL221 P23219 Cyclooxygenase-1 95.31% 90.17%
CHEMBL2581 P07339 Cathepsin D 92.48% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.96% 94.62%
CHEMBL3902 P09211 Glutathione S-transferase Pi 86.92% 93.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.05% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.61% 95.56%

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.
Humulus lupulus

Cross-Links

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PubChem 24321
LOTUS LTS0093308
wikiData Q4462936