Nakorone

Details

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Internal ID df732a03-118e-437c-a9c7-30fe589853a5
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name (3S,5aS,7aS,10bS)-3-hydroxy-4,4,7a,10b-tetramethyl-2,3,5a,6,7,9,10,10a-octahydro-1H-indeno[5,4-b]oxepin-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H28O3/c1-15(2)12(18)7-9-17(4)11-5-6-13(19)16(11,3)10-8-14(17)20-15/h11-12,14,18H,5-10H2,1-4H3/t11?,12-,14-,16-,17-/m0/s1
InChI Key GJHHOLCPYDZIHD-DOXOUGHASA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28O3
Molecular Weight 280.40 g/mol
Exact Mass 280.20384475 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.20
Atomic LogP (AlogP) 3.09
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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(3S,5aS,7aS,10bS)-3-hydroxy-4,4,7a,10b-tetramethyl-2,3,5a,6,7,9,10,10a-octahydro-1H-indeno[5,4-b]oxepin-8-one

2D Structure

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2D Structure of Nakorone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.7592 75.92%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6714 67.14%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.9599 95.99%
OATP1B3 inhibitior + 0.9723 97.23%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8392 83.92%
P-glycoprotein inhibitior - 0.8290 82.90%
P-glycoprotein substrate - 0.9282 92.82%
CYP3A4 substrate + 0.6038 60.38%
CYP2C9 substrate + 0.5319 53.19%
CYP2D6 substrate - 0.7587 75.87%
CYP3A4 inhibition - 0.8167 81.67%
CYP2C9 inhibition - 0.8078 80.78%
CYP2C19 inhibition - 0.8615 86.15%
CYP2D6 inhibition - 0.9641 96.41%
CYP1A2 inhibition - 0.7337 73.37%
CYP2C8 inhibition - 0.8823 88.23%
CYP inhibitory promiscuity - 0.9825 98.25%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6731 67.31%
Eye corrosion - 0.9805 98.05%
Eye irritation - 0.8697 86.97%
Skin irritation + 0.5523 55.23%
Skin corrosion - 0.8883 88.83%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5470 54.70%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.5968 59.68%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6531 65.31%
Acute Oral Toxicity (c) III 0.4939 49.39%
Estrogen receptor binding + 0.7413 74.13%
Androgen receptor binding - 0.4900 49.00%
Thyroid receptor binding + 0.6811 68.11%
Glucocorticoid receptor binding + 0.6908 69.08%
Aromatase binding + 0.6076 60.76%
PPAR gamma - 0.5993 59.93%
Honey bee toxicity - 0.9063 90.63%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8600 86.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.16% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.33% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.41% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.97% 93.04%
CHEMBL1937 Q92769 Histone deacetylase 2 85.49% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.24% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.31% 97.09%
CHEMBL2581 P07339 Cathepsin D 83.82% 98.95%
CHEMBL1871 P10275 Androgen Receptor 83.62% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.61% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.93% 82.69%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 21775361
LOTUS LTS0016162
wikiData Q105009389