Atherospermidine

Details

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Internal ID a4bfa5f3-2ba7-4105-bde7-bf4e8e47928e
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 7-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),9,11,14,16,18-octaen-13-one
SMILES (Canonical) COC1=C2C(=C3C4=CC=CC=C4C(=O)C5=NC=CC1=C35)OCO2
SMILES (Isomeric) COC1=C2C(=C3C4=CC=CC=C4C(=O)C5=NC=CC1=C35)OCO2
InChI InChI=1S/C18H11NO4/c1-21-16-11-6-7-19-14-12(11)13(17-18(16)23-8-22-17)9-4-2-3-5-10(9)15(14)20/h2-7H,8H2,1H3
InChI Key MDFFNDBAEOHIDY-UHFFFAOYSA-N
Popularity 25 references in papers

Physical and Chemical Properties

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Molecular Formula C18H11NO4
Molecular Weight 305.30 g/mol
Exact Mass 305.06880783 g/mol
Topological Polar Surface Area (TPSA) 57.60 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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3912-57-0
Antherospermidine
Liriodenine, 3-methoxy-
E21QMO70E2
4-Methoxy-8H-[1,3]benzodioxolo[6,5,4-de]benzo[g]quinolin-8-one
Noraporphin-7-one, 4,5,6,6a-tetradehydro-3-methoxy-1,2-(methylenedioxy)-
NSC 93680
NSC-93680
4-methoxy-8H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-8-one
8H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-8-one, 4-methoxy-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Atherospermidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.7939 79.39%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6085 60.85%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9606 96.06%
OATP1B3 inhibitior + 0.9681 96.81%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6932 69.32%
P-glycoprotein inhibitior - 0.6789 67.89%
P-glycoprotein substrate - 0.8430 84.30%
CYP3A4 substrate + 0.5730 57.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7812 78.12%
CYP3A4 inhibition + 0.9177 91.77%
CYP2C9 inhibition - 0.5242 52.42%
CYP2C19 inhibition + 0.8236 82.36%
CYP2D6 inhibition - 0.5256 52.56%
CYP1A2 inhibition + 0.9424 94.24%
CYP2C8 inhibition - 0.6932 69.32%
CYP inhibitory promiscuity + 0.9189 91.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5169 51.69%
Eye corrosion - 0.9804 98.04%
Eye irritation - 0.5339 53.39%
Skin irritation - 0.7873 78.73%
Skin corrosion - 0.9649 96.49%
Ames mutagenesis + 0.7436 74.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5448 54.48%
Micronuclear + 0.7474 74.74%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.7872 78.72%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.4728 47.28%
Acute Oral Toxicity (c) III 0.7343 73.43%
Estrogen receptor binding + 0.8126 81.26%
Androgen receptor binding + 0.6137 61.37%
Thyroid receptor binding + 0.6782 67.82%
Glucocorticoid receptor binding + 0.8969 89.69%
Aromatase binding + 0.6202 62.02%
PPAR gamma + 0.6899 68.99%
Honey bee toxicity - 0.8056 80.56%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.5374 53.74%

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
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.17% 89.00%
CHEMBL2581 P07339 Cathepsin D 95.31% 98.95%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 94.47% 96.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.80% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.40% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.18% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.05% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.14% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.68% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.97% 96.77%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.66% 85.14%
CHEMBL2535 P11166 Glucose transporter 88.76% 98.75%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 88.34% 96.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.53% 94.03%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 84.02% 82.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.99% 96.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.00% 95.17%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.73% 100.00%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 82.63% 95.83%
CHEMBL5747 Q92793 CREB-binding protein 81.96% 95.12%
CHEMBL2094121 P14867 GABA-A receptor; alpha-1/beta-3/gamma-2 81.15% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 80.84% 94.73%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.73% 93.10%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 80.59% 80.96%

Cross-Links

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PubChem 77514
NPASS NPC280291
LOTUS LTS0215280
wikiData Q27103894