Pseudomerucathine

Details

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Internal ID 90c3ef35-426c-4ce2-9c32-4af693d0bee1
Taxonomy Phenylpropanoids and polyketides > Cinnamyl alcohols
IUPAC Name (E,3S,4S)-4-amino-1-phenylpent-1-en-3-ol
SMILES (Canonical) CC(C(C=CC1=CC=CC=C1)O)N
SMILES (Isomeric) C[C@@H]([C@H](/C=C/C1=CC=CC=C1)O)N
InChI InChI=1S/C11H15NO/c1-9(12)11(13)8-7-10-5-3-2-4-6-10/h2-9,11,13H,12H2,1H3/b8-7+/t9-,11-/m0/s1
InChI Key MSCXFOZFDVCLHC-QARYBLBWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H15NO
Molecular Weight 177.24 g/mol
Exact Mass 177.115364102 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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(-)-Pseudomerucathine
96861-89-1

2D Structure

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2D Structure of Pseudomerucathine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.8550 85.50%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.6956 69.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9250 92.50%
OATP1B3 inhibitior + 0.9672 96.72%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9096 90.96%
P-glycoprotein inhibitior - 0.9785 97.85%
P-glycoprotein substrate - 0.9401 94.01%
CYP3A4 substrate - 0.7720 77.20%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate + 0.4029 40.29%
CYP3A4 inhibition - 0.8941 89.41%
CYP2C9 inhibition - 0.8397 83.97%
CYP2C19 inhibition - 0.8379 83.79%
CYP2D6 inhibition - 0.9068 90.68%
CYP1A2 inhibition - 0.8493 84.93%
CYP2C8 inhibition - 0.9068 90.68%
CYP inhibitory promiscuity - 0.8199 81.99%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.5089 50.89%
Carcinogenicity (trinary) Non-required 0.6771 67.71%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.8651 86.51%
Skin irritation - 0.6166 61.66%
Skin corrosion + 0.5637 56.37%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7389 73.89%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5633 56.33%
skin sensitisation - 0.5301 53.01%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.8191 81.91%
Acute Oral Toxicity (c) III 0.8942 89.42%
Estrogen receptor binding - 0.8655 86.55%
Androgen receptor binding - 0.8125 81.25%
Thyroid receptor binding - 0.7410 74.10%
Glucocorticoid receptor binding - 0.5595 55.95%
Aromatase binding - 0.8443 84.43%
PPAR gamma - 0.8490 84.90%
Honey bee toxicity - 0.9523 95.23%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.6659 66.59%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.86% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.50% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.33% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.75% 94.62%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.73% 94.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.73% 96.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 89.52% 90.24%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.92% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.11% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 84.33% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 82.09% 94.73%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.79% 93.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.53% 95.50%

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.
Catha edulis

Cross-Links

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PubChem 5459036
LOTUS LTS0073962
wikiData Q104394042