Phenmetrazine

Details

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Internal ID 8b06505d-e4a7-4fb3-8bc1-72f7527603c0
Taxonomy Organoheterocyclic compounds > Oxazinanes > Morpholines > Phenylmorpholines
IUPAC Name 3-methyl-2-phenylmorpholine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H15NO/c1-9-11(13-8-7-12-9)10-5-3-2-4-6-10/h2-6,9,11-12H,7-8H2,1H3
InChI Key OOBHFESNSZDWIU-UHFFFAOYSA-N
Popularity 0 references 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) 21.30 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.74
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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3-Methyl-2-phenylmorpholine
Oxazimedrine
Phenmetrazin
2-Phenyl-3-methylmorpholine
Psychamine A 66
Probese-P
134-49-6
Fenmetrazin
Fenmetrazina
Defenmetrazin
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phenmetrazine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.8875 88.75%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.6181 61.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9457 94.57%
OATP1B3 inhibitior + 0.9464 94.64%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9767 97.67%
P-glycoprotein inhibitior - 0.9829 98.29%
P-glycoprotein substrate - 0.9101 91.01%
CYP3A4 substrate - 0.6688 66.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5143 51.43%
CYP3A4 inhibition - 0.8524 85.24%
CYP2C9 inhibition - 0.9188 91.88%
CYP2C19 inhibition - 0.7002 70.02%
CYP2D6 inhibition - 0.6846 68.46%
CYP1A2 inhibition - 0.6065 60.65%
CYP2C8 inhibition - 0.8068 80.68%
CYP inhibitory promiscuity - 0.7188 71.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6373 63.73%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9554 95.54%
Skin irritation - 0.5512 55.12%
Skin corrosion - 0.5697 56.97%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4802 48.02%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8643 86.43%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7510 75.10%
Acute Oral Toxicity (c) II 0.7451 74.51%
Estrogen receptor binding - 0.9239 92.39%
Androgen receptor binding - 0.7822 78.22%
Thyroid receptor binding - 0.8470 84.70%
Glucocorticoid receptor binding - 0.9565 95.65%
Aromatase binding - 0.9028 90.28%
PPAR gamma - 0.8322 83.22%
Honey bee toxicity - 0.9581 95.81%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.9639 96.39%

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
CHEMBL1951 P21397 Monoamine oxidase A 92.33% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.25% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.92% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.69% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.60% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.06% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.29% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.56% 97.25%
CHEMBL5028 O14672 ADAM10 80.08% 97.50%

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.
Marsdenia roylei

Cross-Links

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PubChem 4762
LOTUS LTS0045071
wikiData Q3329406