(2S)-2-(ethylamino)-2-thiophen-2-ylcyclohexan-1-one

Details

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Internal ID 4f9d2c21-9d29-425c-81d3-fdde47c79e21
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Amines > Aralkylamines
IUPAC Name (2S)-2-(ethylamino)-2-thiophen-2-ylcyclohexan-1-one
SMILES (Canonical) CCNC1(CCCCC1=O)C2=CC=CS2
SMILES (Isomeric) CCN[C@]1(CCCCC1=O)C2=CC=CS2
InChI InChI=1S/C12H17NOS/c1-2-13-12(11-7-5-9-15-11)8-4-3-6-10(12)14/h5,7,9,13H,2-4,6,8H2,1H3/t12-/m0/s1
InChI Key QAXBVGVYDCAVLV-LBPRGKRZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H17NOS
Molecular Weight 223.34 g/mol
Exact Mass 223.10308534 g/mol
Topological Polar Surface Area (TPSA) 57.30 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.70
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-2-(ethylamino)-2-thiophen-2-ylcyclohexan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.8052 80.52%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4991 49.91%
OATP2B1 inhibitior - 0.8491 84.91%
OATP1B1 inhibitior + 0.8974 89.74%
OATP1B3 inhibitior + 0.9450 94.50%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.9123 91.23%
P-glycoprotein inhibitior - 0.9753 97.53%
P-glycoprotein substrate - 0.8935 89.35%
CYP3A4 substrate - 0.5777 57.77%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate + 0.4132 41.32%
CYP3A4 inhibition - 0.8310 83.10%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9025 90.25%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition - 0.8962 89.62%
CYP inhibitory promiscuity + 0.8240 82.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.6545 65.45%
Eye corrosion - 0.9734 97.34%
Eye irritation + 0.5364 53.64%
Skin irritation - 0.7073 70.73%
Skin corrosion - 0.8450 84.50%
Ames mutagenesis - 0.5337 53.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5563 55.63%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.5184 51.84%
skin sensitisation - 0.8114 81.14%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7989 79.89%
Acute Oral Toxicity (c) III 0.6423 64.23%
Estrogen receptor binding - 0.8146 81.46%
Androgen receptor binding - 0.8512 85.12%
Thyroid receptor binding - 0.6779 67.79%
Glucocorticoid receptor binding - 0.8070 80.70%
Aromatase binding - 0.8476 84.76%
PPAR gamma - 0.5122 51.22%
Honey bee toxicity - 0.9704 97.04%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.6947 69.47%

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
CHEMBL2581 P07339 Cathepsin D 96.40% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 95.69% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.48% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.05% 91.11%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 89.25% 85.30%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.30% 96.09%
CHEMBL4578 Q14680 Maternal embryonic leucine zipper kinase 82.65% 81.58%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.32% 93.03%
CHEMBL4072 P07858 Cathepsin B 82.23% 93.67%
CHEMBL2916 O14746 Telomerase reverse transcriptase 82.02% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.59% 95.50%
CHEMBL1937 Q92769 Histone deacetylase 2 81.32% 94.75%
CHEMBL1944 P08473 Neprilysin 80.81% 92.63%
CHEMBL5408 Q9UHD2 Serine/threonine-protein kinase TBK1 80.71% 90.48%

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.
Anemarrhena asphodeloides
Euphorbia royleana

Cross-Links

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PubChem 73416012
NPASS NPC154346