N-(2-(4-(((2E)-5-(3,3-Dimethyl-2-oxiranyl)-4-hydroxy-3-methyl-2-penten-1-yl)oxy)phenyl)ethyl)benzamide

Details

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Internal ID 69f92fc9-86cd-4fa7-8bfc-ac6b2d7049a0
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzamides
IUPAC Name N-[2-[4-[(E)-5-(3,3-dimethyloxiran-2-yl)-4-hydroxy-3-methylpent-2-enoxy]phenyl]ethyl]benzamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H31NO4/c1-18(22(27)17-23-25(2,3)30-23)14-16-29-21-11-9-19(10-12-21)13-15-26-24(28)20-7-5-4-6-8-20/h4-12,14,22-23,27H,13,15-17H2,1-3H3,(H,26,28)/b18-14+
InChI Key QQKKFVXSQXUHPI-NBVRZTHBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H31NO4
Molecular Weight 409.50 g/mol
Exact Mass 409.22530847 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.91
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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DTXSID701112661
N-(2-(4-(((2E)-5-(3,3-Dimethyl-2-oxiranyl)-4-hydroxy-3-methyl-2-penten-1-yl)oxy)phenyl)ethyl)benzamide
N-[2-[4-[[(2E)-5-(3,3-Dimethyl-2-oxiranyl)-4-hydroxy-3-methyl-2-penten-1-yl]oxy]phenyl]ethyl]benzamide
RefChem:1090930
DTXCID701544266
Severin
Severine
Acidissiminol epoxide
N-[2-[4-[(E)-5-(3,3-dimethyloxiran-2-yl)-4-hydroxy-3-methylpent-2-enoxy]phenyl]ethyl]benzamide
Severinia
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of N-(2-(4-(((2E)-5-(3,3-Dimethyl-2-oxiranyl)-4-hydroxy-3-methyl-2-penten-1-yl)oxy)phenyl)ethyl)benzamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9796 97.96%
Caco-2 - 0.7524 75.24%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7419 74.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9037 90.37%
OATP1B3 inhibitior + 0.9372 93.72%
MATE1 inhibitior - 0.8654 86.54%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9607 96.07%
P-glycoprotein inhibitior + 0.7881 78.81%
P-glycoprotein substrate + 0.6794 67.94%
CYP3A4 substrate + 0.6677 66.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7990 79.90%
CYP3A4 inhibition + 0.5441 54.41%
CYP2C9 inhibition - 0.6966 69.66%
CYP2C19 inhibition - 0.6512 65.12%
CYP2D6 inhibition - 0.7755 77.55%
CYP1A2 inhibition - 0.7120 71.20%
CYP2C8 inhibition + 0.7936 79.36%
CYP inhibitory promiscuity + 0.5390 53.90%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8628 86.28%
Carcinogenicity (trinary) Non-required 0.5836 58.36%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.9603 96.03%
Skin irritation - 0.7560 75.60%
Skin corrosion - 0.9334 93.34%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8945 89.45%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8059 80.59%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.7681 76.81%
Acute Oral Toxicity (c) III 0.6132 61.32%
Estrogen receptor binding + 0.6971 69.71%
Androgen receptor binding + 0.6938 69.38%
Thyroid receptor binding + 0.5801 58.01%
Glucocorticoid receptor binding + 0.6234 62.34%
Aromatase binding + 0.5460 54.60%
PPAR gamma + 0.7192 71.92%
Honey bee toxicity - 0.7790 77.90%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.8837 88.37%

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 96.05% 96.09%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 95.70% 89.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.44% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 93.55% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.52% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.24% 94.73%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 93.00% 87.67%
CHEMBL240 Q12809 HERG 92.86% 89.76%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 92.22% 96.67%
CHEMBL2039 P27338 Monoamine oxidase B 91.76% 92.51%
CHEMBL2581 P07339 Cathepsin D 91.34% 98.95%
CHEMBL2179 P04062 Beta-glucocerebrosidase 90.48% 85.31%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.01% 94.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.75% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.63% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.00% 95.56%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 87.39% 89.67%
CHEMBL4208 P20618 Proteasome component C5 85.52% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.59% 96.00%
CHEMBL2535 P11166 Glucose transporter 84.43% 98.75%
CHEMBL3902 P09211 Glutathione S-transferase Pi 83.59% 93.81%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.77% 94.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.39% 81.11%

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.
Fritillaria sewerzowi

Cross-Links

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PubChem 5363185
LOTUS LTS0108634
wikiData Q105225891