Cycloacetylcuparene

Details

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Internal ID 443a820f-691c-4cf0-86f7-6b34a97a5817
Taxonomy Benzenoids > Indanes
IUPAC Name 1-(3a,6,8b-trimethyl-1,2,3,4-tetrahydrocyclopenta[a]inden-7-yl)ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O/c1-11-8-13-10-16(3)6-5-7-17(16,4)15(13)9-14(11)12(2)18/h8-9H,5-7,10H2,1-4H3
InChI Key MFCQMRORMOZNKH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O
Molecular Weight 242.36 g/mol
Exact Mass 242.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.20
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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MFCQMRORMOZNKH-UHFFFAOYSA-N
1-(3a,6,8a-Trimethyl-1,2,3,3a,8,8a-hexahydrocyclopenta[a]inden-5-yl)ethanone #

2D Structure

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2D Structure of Cycloacetylcuparene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9790 97.90%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.4261 42.61%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.8931 89.31%
OATP1B3 inhibitior + 0.9677 96.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.7589 75.89%
P-glycoprotein inhibitior - 0.9239 92.39%
P-glycoprotein substrate - 0.8405 84.05%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7979 79.79%
CYP3A4 inhibition - 0.8945 89.45%
CYP2C9 inhibition - 0.8360 83.60%
CYP2C19 inhibition - 0.7895 78.95%
CYP2D6 inhibition - 0.9419 94.19%
CYP1A2 inhibition - 0.5258 52.58%
CYP2C8 inhibition - 0.7917 79.17%
CYP inhibitory promiscuity - 0.7946 79.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5390 53.90%
Eye corrosion - 0.9291 92.91%
Eye irritation + 0.7958 79.58%
Skin irritation + 0.5758 57.58%
Skin corrosion - 0.9856 98.56%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3758 37.58%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6791 67.91%
skin sensitisation + 0.6899 68.99%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5545 55.45%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.5720 57.20%
Acute Oral Toxicity (c) IV 0.5425 54.25%
Estrogen receptor binding - 0.7194 71.94%
Androgen receptor binding - 0.5485 54.85%
Thyroid receptor binding - 0.5882 58.82%
Glucocorticoid receptor binding - 0.7238 72.38%
Aromatase binding - 0.5194 51.94%
PPAR gamma - 0.6657 66.57%
Honey bee toxicity - 0.9552 95.52%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9918 99.18%

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 94.16% 91.11%
CHEMBL4208 P20618 Proteasome component C5 91.98% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.42% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.41% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.63% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.13% 91.07%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 85.07% 91.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.71% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 83.62% 94.73%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.58% 93.03%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.79% 93.04%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.42% 95.50%

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.
Atractylodes lancea

Cross-Links

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PubChem 540090
NPASS NPC109970