Oldhamactam

Details

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Internal ID 84911456-9ba3-46dd-a51e-6f5dd5140367
Taxonomy Alkaloids and derivatives > Aristolactams
IUPAC Name 6-hydroxy-13,14,15-trimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one
SMILES (Canonical) COC1=C(C(=C2C3=C(C=C4C(=C31)C=CC=C4O)NC2=O)OC)OC
SMILES (Isomeric) COC1=C(C(=C2C3=C(C=C4C(=C31)C=CC=C4O)NC2=O)OC)OC
InChI InChI=1S/C18H15NO5/c1-22-15-12-8-5-4-6-11(20)9(8)7-10-13(12)14(18(21)19-10)16(23-2)17(15)24-3/h4-7,20H,1-3H3,(H,19,21)
InChI Key XPAJKJNXGTXSLZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H15NO5
Molecular Weight 325.30 g/mol
Exact Mass 325.09502258 g/mol
Topological Polar Surface Area (TPSA) 77.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.29
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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CHEMBL412823

2D Structure

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2D Structure of Oldhamactam

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9868 98.68%
Caco-2 + 0.8539 85.39%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.6060 60.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9273 92.73%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6469 64.69%
P-glycoprotein inhibitior - 0.6176 61.76%
P-glycoprotein substrate - 0.8472 84.72%
CYP3A4 substrate + 0.6161 61.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8343 83.43%
CYP3A4 inhibition - 0.5962 59.62%
CYP2C9 inhibition - 0.9211 92.11%
CYP2C19 inhibition - 0.8505 85.05%
CYP2D6 inhibition - 0.8397 83.97%
CYP1A2 inhibition + 0.7746 77.46%
CYP2C8 inhibition + 0.5063 50.63%
CYP inhibitory promiscuity + 0.5298 52.98%
UGT catelyzed - 0.7638 76.38%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4580 45.80%
Eye corrosion - 0.9935 99.35%
Eye irritation - 0.6362 63.62%
Skin irritation - 0.8634 86.34%
Skin corrosion - 0.9739 97.39%
Ames mutagenesis + 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6330 63.30%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.6178 61.78%
skin sensitisation - 0.9392 93.92%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.7201 72.01%
Acute Oral Toxicity (c) III 0.4359 43.59%
Estrogen receptor binding + 0.8456 84.56%
Androgen receptor binding + 0.6624 66.24%
Thyroid receptor binding + 0.7624 76.24%
Glucocorticoid receptor binding + 0.8073 80.73%
Aromatase binding + 0.5823 58.23%
PPAR gamma + 0.8271 82.71%
Honey bee toxicity - 0.9324 93.24%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.7955 79.55%

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 99.27% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.34% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.80% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.65% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.41% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.73% 85.14%
CHEMBL2535 P11166 Glucose transporter 92.64% 98.75%
CHEMBL1937 Q92769 Histone deacetylase 2 92.27% 94.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.05% 99.15%
CHEMBL2581 P07339 Cathepsin D 89.38% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.15% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.05% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.49% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 87.45% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 87.11% 91.71%
CHEMBL4208 P20618 Proteasome component C5 86.51% 90.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.21% 93.03%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.12% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 83.01% 93.31%

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.
Annona squamosa
Fissistigma oldhamii

Cross-Links

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PubChem 44422603
NPASS NPC219170
ChEMBL CHEMBL412823
LOTUS LTS0080839
wikiData Q105338069