Aristotelone

Details

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Internal ID 6143b90c-9d8d-445b-b753-237480d0ff06
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolines
IUPAC Name 2',2',7'-trimethylspiro[1H-indole-2,6'-3-azatricyclo[5.2.2.04,8]undecane]-3-one
SMILES (Canonical) CC1(C2CCC3(C(C2)C(N1)CC34C(=O)C5=CC=CC=C5N4)C)C
SMILES (Isomeric) CC1(C2CCC3(C(C2)C(N1)CC34C(=O)C5=CC=CC=C5N4)C)C
InChI InChI=1S/C20H26N2O/c1-18(2)12-8-9-19(3)14(10-12)16(21-18)11-20(19)17(23)13-6-4-5-7-15(13)22-20/h4-7,12,14,16,21-22H,8-11H2,1-3H3
InChI Key RDOJZOUKVJESIV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26N2O
Molecular Weight 310.40 g/mol
Exact Mass 310.204513457 g/mol
Topological Polar Surface Area (TPSA) 41.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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5222-85-5
DTXSID60966597
NSC286325
ARISTOTELONE B668273K007
NSC-286325
59863-01-3
3a,8,8-Trimethyl-1,2,3a,4,5,6,7,7a-octahydrospiro[1,6-(epiminomethano)indene-3,2'-indol]-3'(1'H)-one

2D Structure

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2D Structure of Aristotelone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.9379 93.79%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5714 57.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8992 89.92%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.5263 52.63%
P-glycoprotein inhibitior - 0.8387 83.87%
P-glycoprotein substrate - 0.6874 68.74%
CYP3A4 substrate + 0.6769 67.69%
CYP2C9 substrate - 0.5984 59.84%
CYP2D6 substrate - 0.7572 75.72%
CYP3A4 inhibition - 0.8373 83.73%
CYP2C9 inhibition - 0.7123 71.23%
CYP2C19 inhibition - 0.5693 56.93%
CYP2D6 inhibition - 0.7088 70.88%
CYP1A2 inhibition - 0.7523 75.23%
CYP2C8 inhibition - 0.5980 59.80%
CYP inhibitory promiscuity + 0.6020 60.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5996 59.96%
Eye corrosion - 0.9832 98.32%
Eye irritation - 0.9924 99.24%
Skin irritation - 0.7505 75.05%
Skin corrosion - 0.8733 87.33%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5088 50.88%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.5695 56.95%
skin sensitisation - 0.7935 79.35%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.5822 58.22%
Acute Oral Toxicity (c) III 0.6035 60.35%
Estrogen receptor binding + 0.6967 69.67%
Androgen receptor binding + 0.6834 68.34%
Thyroid receptor binding + 0.5729 57.29%
Glucocorticoid receptor binding - 0.6702 67.02%
Aromatase binding + 0.6960 69.60%
PPAR gamma + 0.6195 61.95%
Honey bee toxicity - 0.8174 81.74%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.8834 88.34%

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
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 98.56% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.45% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.84% 95.56%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 94.56% 94.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.24% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.57% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.43% 94.62%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.97% 93.40%
CHEMBL2581 P07339 Cathepsin D 90.44% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.33% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 89.60% 94.75%
CHEMBL221 P23219 Cyclooxygenase-1 89.42% 90.17%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 88.60% 94.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.56% 97.25%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 86.51% 88.84%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.42% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.16% 97.14%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.17% 92.67%

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.
Aristotelia chilensis

Cross-Links

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PubChem 323715
LOTUS LTS0090511
wikiData Q82949013