(R)-2-methyl-3-phenylpropanal

Details

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Internal ID d38183a8-68d1-46df-8df4-a05947ef2700
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name (2R)-2-methyl-3-phenylpropanal
SMILES (Canonical) CC(CC1=CC=CC=C1)C=O
SMILES (Isomeric) C[C@H](CC1=CC=CC=C1)C=O
InChI InChI=1S/C10H12O/c1-9(8-11)7-10-5-3-2-4-6-10/h2-6,8-9H,7H2,1H3/t9-/m1/s1
InChI Key HEPHYCJJLAUKSB-SECBINFHSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O
Molecular Weight 148.20 g/mol
Exact Mass 148.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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(R)-2-Benzylpropanal
SCHEMBL3484487
HEPHYCJJLAUKSB-SECBINFHSA-N

2D Structure

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2D Structure of (R)-2-methyl-3-phenylpropanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.9345 93.45%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.5494 54.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9271 92.71%
OATP1B3 inhibitior + 0.9646 96.46%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8924 89.24%
P-glycoprotein inhibitior - 0.9929 99.29%
P-glycoprotein substrate - 0.9604 96.04%
CYP3A4 substrate - 0.7506 75.06%
CYP2C9 substrate - 0.5824 58.24%
CYP2D6 substrate - 0.7235 72.35%
CYP3A4 inhibition - 0.9708 97.08%
CYP2C9 inhibition - 0.9588 95.88%
CYP2C19 inhibition - 0.9424 94.24%
CYP2D6 inhibition - 0.9516 95.16%
CYP1A2 inhibition - 0.5627 56.27%
CYP2C8 inhibition - 0.9752 97.52%
CYP inhibitory promiscuity - 0.8435 84.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5664 56.64%
Carcinogenicity (trinary) Non-required 0.6597 65.97%
Eye corrosion + 0.9892 98.92%
Eye irritation + 0.9235 92.35%
Skin irritation + 0.9437 94.37%
Skin corrosion + 0.6507 65.07%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6918 69.18%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.5012 50.12%
skin sensitisation + 0.9757 97.57%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6536 65.36%
Acute Oral Toxicity (c) III 0.9133 91.33%
Estrogen receptor binding - 0.9393 93.93%
Androgen receptor binding - 0.7646 76.46%
Thyroid receptor binding - 0.9088 90.88%
Glucocorticoid receptor binding - 0.8652 86.52%
Aromatase binding - 0.8342 83.42%
PPAR gamma - 0.8839 88.39%
Honey bee toxicity - 0.9476 94.76%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.8905 89.05%

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 98.21% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 95.54% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.15% 95.56%
CHEMBL3492 P49721 Proteasome Macropain subunit 90.12% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.20% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 87.95% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.59% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.30% 94.62%
CHEMBL4072 P07858 Cathepsin B 82.99% 93.67%
CHEMBL3891 P07384 Calpain 1 81.25% 93.04%

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.
Conioselinum anthriscoides
Ligusticum officinale
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 1549658
NPASS NPC44864