2-Benzylbenzoic acid

Details

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Internal ID 1cd9612a-8f95-4d20-b2a0-33a5b302d263
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylmethanes
IUPAC Name 2-benzylbenzoic acid
SMILES (Canonical) C1=CC=C(C=C1)CC2=CC=CC=C2C(=O)O
SMILES (Isomeric) C1=CC=C(C=C1)CC2=CC=CC=C2C(=O)O
InChI InChI=1S/C14H12O2/c15-14(16)13-9-5-4-8-12(13)10-11-6-2-1-3-7-11/h1-9H,10H2,(H,15,16)
InChI Key FESDHLLVLYZNFY-UHFFFAOYSA-N
Popularity 45 references in papers

Physical and Chemical Properties

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Molecular Formula C14H12O2
Molecular Weight 212.24 g/mol
Exact Mass 212.083729621 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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612-35-1
alpha-Phenyl-o-toluic acid
o-Benzylbenzoic acid
2-(PHENYLMETHYL)BENZOIC ACID
UNII-XGQ9B53P0K
XGQ9B53P0K
CHEMBL1879588
EINECS 210-305-2
MFCD00002484
NSC-74872
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Benzylbenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.8519 85.19%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.8217 82.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9413 94.13%
OATP1B3 inhibitior + 0.9387 93.87%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7307 73.07%
P-glycoprotein inhibitior - 0.9699 96.99%
P-glycoprotein substrate - 0.9710 97.10%
CYP3A4 substrate - 0.8031 80.31%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.8825 88.25%
CYP3A4 inhibition - 0.9478 94.78%
CYP2C9 inhibition - 0.7563 75.63%
CYP2C19 inhibition - 0.8445 84.45%
CYP2D6 inhibition - 0.9275 92.75%
CYP1A2 inhibition - 0.6466 64.66%
CYP2C8 inhibition - 0.8450 84.50%
CYP inhibitory promiscuity - 0.7273 72.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5651 56.51%
Carcinogenicity (trinary) Non-required 0.7591 75.91%
Eye corrosion - 0.9489 94.89%
Eye irritation + 0.9171 91.71%
Skin irritation + 0.8242 82.42%
Skin corrosion - 0.8446 84.46%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8761 87.61%
Micronuclear - 0.7277 72.77%
Hepatotoxicity + 0.5949 59.49%
skin sensitisation + 0.6681 66.81%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7088 70.88%
Estrogen receptor binding + 0.6188 61.88%
Androgen receptor binding - 0.8401 84.01%
Thyroid receptor binding - 0.6439 64.39%
Glucocorticoid receptor binding + 0.6701 67.01%
Aromatase binding + 0.8468 84.68%
PPAR gamma + 0.8571 85.71%
Honey bee toxicity - 0.9284 92.84%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity + 0.9855 98.55%

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
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 94.00% 95.50%
CHEMBL2581 P07339 Cathepsin D 91.40% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.88% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.65% 96.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.60% 93.00%
CHEMBL221 P23219 Cyclooxygenase-1 83.61% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.11% 86.33%

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.
Erigeron canadensis
Populus tremuloides

Cross-Links

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PubChem 11924
NPASS NPC255676
LOTUS LTS0085290
wikiData Q27293838