3,4-Dimethyl-5-phenyl-1,3-oxazolidine

Details

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Internal ID bcdc1c1b-45e3-4f52-b740-777dca6d97f9
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 3,4-dimethyl-5-phenyl-1,3-oxazolidine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H15NO/c1-9-11(13-8-12(9)2)10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3
InChI Key POZQVPIDBKNJTK-UHFFFAOYSA-N
Popularity 4 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) 12.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.04
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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66574-19-4
DTXSID10985172
RefChem:910641
DTXCID90960684
3,4-Dimethyl-5-phenyloxazolidine
NSC354436
SCHEMBL11157070
NSC354433
NSC354435
NSC-354433
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,4-Dimethyl-5-phenyl-1,3-oxazolidine

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 + 0.9456 94.56%
Blood Brain Barrier + 0.9320 93.20%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4909 49.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9299 92.99%
OATP1B3 inhibitior + 0.9440 94.40%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9370 93.70%
P-glycoprotein inhibitior - 0.9836 98.36%
P-glycoprotein substrate - 0.8906 89.06%
CYP3A4 substrate - 0.6424 64.24%
CYP2C9 substrate - 0.7957 79.57%
CYP2D6 substrate - 0.7356 73.56%
CYP3A4 inhibition - 0.9360 93.60%
CYP2C9 inhibition - 0.8677 86.77%
CYP2C19 inhibition - 0.6534 65.34%
CYP2D6 inhibition - 0.7586 75.86%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9338 93.38%
CYP inhibitory promiscuity - 0.6233 62.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5565 55.65%
Eye corrosion - 0.9693 96.93%
Eye irritation - 0.9456 94.56%
Skin irritation - 0.6412 64.12%
Skin corrosion - 0.8073 80.73%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4729 47.29%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5301 53.01%
skin sensitisation - 0.8355 83.55%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.8558 85.58%
Acute Oral Toxicity (c) III 0.4878 48.78%
Estrogen receptor binding - 0.8159 81.59%
Androgen receptor binding - 0.6570 65.70%
Thyroid receptor binding - 0.8699 86.99%
Glucocorticoid receptor binding - 0.9089 90.89%
Aromatase binding - 0.8943 89.43%
PPAR gamma - 0.8793 87.93%
Honey bee toxicity - 0.9487 94.87%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity - 0.6017 60.17%

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 91.87% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.27% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 90.19% 91.49%
CHEMBL2581 P07339 Cathepsin D 88.75% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.75% 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.
Ephedra sinica

Cross-Links

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PubChem 434666
NPASS NPC14757