Stigmalactam

Details

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Internal ID 2cb0b5f3-6479-4f50-b85a-8e2490d1c7b0
Taxonomy Alkaloids and derivatives > Aristolactams
IUPAC Name 4-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=CC(=CC4=C31)O)NC2=O)OC)OC
SMILES (Isomeric) COC1=C(C(=C2C3=C(C=C4C=CC(=CC4=C31)O)NC2=O)OC)OC
InChI InChI=1S/C18H15NO5/c1-22-15-12-10-7-9(20)5-4-8(10)6-11-13(12)14(18(21)19-11)16(23-2)17(15)24-3/h4-7,20H,1-3H3,(H,19,21)
InChI Key GHYWNOWXFZMSSL-UHFFFAOYSA-N
Popularity 5 references 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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CHEMBL486789
AKOS040735133
4-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

2D Structure

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2D Structure of Stigmalactam

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 + 0.8214 82.14%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6060 60.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8534 85.34%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.5929 59.29%
P-glycoprotein inhibitior - 0.5991 59.91%
P-glycoprotein substrate - 0.7415 74.15%
CYP3A4 substrate + 0.5706 57.06%
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 + 0.6000 60.00%
CYP inhibitory promiscuity + 0.5298 52.98%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4580 45.80%
Eye corrosion - 0.9935 99.35%
Eye irritation - 0.6268 62.68%
Skin irritation - 0.8634 86.34%
Skin corrosion - 0.9739 97.39%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5569 55.69%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.5947 59.47%
skin sensitisation - 0.9392 93.92%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.7300 73.00%
Acute Oral Toxicity (c) III 0.4359 43.59%
Estrogen receptor binding + 0.7363 73.63%
Androgen receptor binding + 0.7251 72.51%
Thyroid receptor binding + 0.7408 74.08%
Glucocorticoid receptor binding + 0.7852 78.52%
Aromatase binding + 0.5669 56.69%
PPAR gamma + 0.8031 80.31%
Honey bee toxicity - 0.9374 93.74%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5600 56.00%
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 98.60% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.42% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.76% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.91% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 91.29% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.59% 86.33%
CHEMBL2535 P11166 Glucose transporter 89.04% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.82% 99.23%
CHEMBL4208 P20618 Proteasome component C5 86.78% 90.00%
CHEMBL2581 P07339 Cathepsin D 86.31% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.01% 99.15%
CHEMBL5491 P30291 Serine/threonine-protein kinase WEE1 85.97% 97.46%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.76% 96.09%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 83.16% 94.97%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.77% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 81.94% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.44% 91.71%

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 balansae
Fissistigma oldhamii

Cross-Links

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PubChem 10314215
NPASS NPC180253
LOTUS LTS0022955
wikiData Q105008814