2,3,4-Trimethyl-5-phenyloxazolidine

Details

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Internal ID 35213ade-3f4e-406c-8ecc-880f3f00484f
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 2,3,4-trimethyl-5-phenyl-1,3-oxazolidine
SMILES (Canonical) CC1C(OC(N1C)C)C2=CC=CC=C2
SMILES (Isomeric) CC1C(OC(N1C)C)C2=CC=CC=C2
InChI InChI=1S/C12H17NO/c1-9-12(14-10(2)13(9)3)11-7-5-4-6-8-11/h4-10,12H,1-3H3
InChI Key HHPJDYZRNRHFBT-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H17NO
Molecular Weight 191.27 g/mol
Exact Mass 191.131014166 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.42
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,3,4-Trimethyl-5-phenyloxazolidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9634 96.34%
Caco-2 + 0.8884 88.84%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5890 58.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9323 93.23%
OATP1B3 inhibitior + 0.9485 94.85%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8848 88.48%
BSEP inhibitior - 0.8749 87.49%
P-glycoprotein inhibitior - 0.9558 95.58%
P-glycoprotein substrate - 0.9433 94.33%
CYP3A4 substrate - 0.6798 67.98%
CYP2C9 substrate - 0.7957 79.57%
CYP2D6 substrate - 0.7356 73.56%
CYP3A4 inhibition - 0.9182 91.82%
CYP2C9 inhibition - 0.8302 83.02%
CYP2C19 inhibition - 0.6151 61.51%
CYP2D6 inhibition - 0.8186 81.86%
CYP1A2 inhibition + 0.5595 55.95%
CYP2C8 inhibition - 0.9463 94.63%
CYP inhibitory promiscuity + 0.6361 63.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.4694 46.94%
Eye corrosion - 0.9608 96.08%
Eye irritation - 0.8431 84.31%
Skin irritation - 0.6550 65.50%
Skin corrosion - 0.9114 91.14%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3936 39.36%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8817 88.17%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5837 58.37%
Nephrotoxicity - 0.6661 66.61%
Acute Oral Toxicity (c) III 0.6582 65.82%
Estrogen receptor binding - 0.7994 79.94%
Androgen receptor binding - 0.6337 63.37%
Thyroid receptor binding - 0.8013 80.13%
Glucocorticoid receptor binding - 0.9061 90.61%
Aromatase binding - 0.8243 82.43%
PPAR gamma - 0.8382 83.82%
Honey bee toxicity - 0.9562 95.62%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity - 0.8433 84.33%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.41% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.93% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.58% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.35% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 85.50% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 83.48% 91.49%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.41% 100.00%

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.
Angelica taiwaniana
Ephedra sinica

Cross-Links

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PubChem 5322112
NPASS NPC176790