Atractylenolactam

Details

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Internal ID 3be425a6-ac73-40a4-8189-02747144cbc5
Taxonomy Organoheterocyclic compounds > Indoles and derivatives
IUPAC Name (4aS,8aS)-3,8a-dimethyl-5-methylidene-1,4,4a,6,7,8-hexahydrobenzo[f]indol-2-one
SMILES (Canonical) CC1=C2CC3C(=C)CCCC3(C=C2NC1=O)C
SMILES (Isomeric) CC1=C2C[C@H]3C(=C)CCC[C@@]3(C=C2NC1=O)C
InChI InChI=1S/C15H19NO/c1-9-5-4-6-15(3)8-13-11(7-12(9)15)10(2)14(17)16-13/h8,12H,1,4-7H2,2-3H3,(H,16,17)/t12-,15+/m0/s1
InChI Key RXTVBISZHPGQKT-SWLSCSKDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H19NO
Molecular Weight 229.32 g/mol
Exact Mass 229.146664230 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.08
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Atractylenolactam

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.8337 83.37%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.3779 37.79%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.8872 88.72%
OATP1B3 inhibitior + 0.9295 92.95%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.8788 87.88%
P-glycoprotein inhibitior - 0.9271 92.71%
P-glycoprotein substrate - 0.7431 74.31%
CYP3A4 substrate + 0.5368 53.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9019 90.19%
CYP3A4 inhibition - 0.7015 70.15%
CYP2C9 inhibition + 0.5207 52.07%
CYP2C19 inhibition + 0.5753 57.53%
CYP2D6 inhibition - 0.8658 86.58%
CYP1A2 inhibition - 0.6043 60.43%
CYP2C8 inhibition - 0.8862 88.62%
CYP inhibitory promiscuity + 0.6503 65.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4859 48.59%
Eye corrosion - 0.9786 97.86%
Eye irritation - 0.8885 88.85%
Skin irritation - 0.7489 74.89%
Skin corrosion - 0.9289 92.89%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7378 73.78%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.8500 85.00%
skin sensitisation - 0.7719 77.19%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4708 47.08%
Acute Oral Toxicity (c) III 0.5977 59.77%
Estrogen receptor binding - 0.6000 60.00%
Androgen receptor binding + 0.5378 53.78%
Thyroid receptor binding - 0.5053 50.53%
Glucocorticoid receptor binding + 0.6028 60.28%
Aromatase binding - 0.7107 71.07%
PPAR gamma - 0.5802 58.02%
Honey bee toxicity - 0.8885 88.85%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9926 99.26%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.48% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.98% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.41% 91.11%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 91.57% 93.03%
CHEMBL2581 P07339 Cathepsin D 89.97% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.08% 97.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.05% 96.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.47% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.29% 85.14%
CHEMBL1937 Q92769 Histone deacetylase 2 85.07% 94.75%
CHEMBL5408 Q9UHD2 Serine/threonine-protein kinase TBK1 84.80% 90.48%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.95% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.03% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.99% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.97% 100.00%

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
Atractylodes macrocephala

Cross-Links

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PubChem 101707484
NPASS NPC173421
LOTUS LTS0102990
wikiData Q105247284