Aspidospermidin-17-ol, 19,21-epoxy-15,16-dimethoxy-1-(1-oxopropyl)-

Details

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Internal ID e8c8ef8d-c43f-4e2a-94a2-f1599b1a33a9
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 1-(7-hydroxy-8,9-dimethoxy-17-oxa-5,15-diazahexacyclo[13.4.3.01,16.04,12.06,11.012,16]docosa-6,8,10-trien-5-yl)propan-1-one
SMILES (Canonical) CCC(=O)N1C2CCC34CCCN5C3(C2(CC5)C6=CC(=C(C(=C61)O)OC)OC)OCC4
SMILES (Isomeric) CCC(=O)N1C2CCC34CCCN5C3(C2(CC5)C6=CC(=C(C(=C61)O)OC)OC)OCC4
InChI InChI=1S/C24H32N2O5/c1-4-18(27)26-17-6-8-22-7-5-11-25-12-9-23(17,24(22,25)31-13-10-22)15-14-16(29-2)21(30-3)20(28)19(15)26/h14,17,28H,4-13H2,1-3H3
InChI Key BJYVZJQGRUSSBS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H32N2O5
Molecular Weight 428.50 g/mol
Exact Mass 428.23112213 g/mol
Topological Polar Surface Area (TPSA) 71.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.17
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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Aspidospermidin-17-ol, 19,21-epoxy-15,16-dimethoxy-1-(1-oxopropyl)-

2D Structure

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2D Structure of Aspidospermidin-17-ol, 19,21-epoxy-15,16-dimethoxy-1-(1-oxopropyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9554 95.54%
Caco-2 + 0.6732 67.32%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6654 66.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8478 84.78%
OATP1B3 inhibitior + 0.9416 94.16%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.7261 72.61%
P-glycoprotein inhibitior - 0.6573 65.73%
P-glycoprotein substrate + 0.5547 55.47%
CYP3A4 substrate + 0.6591 65.91%
CYP2C9 substrate - 0.5976 59.76%
CYP2D6 substrate - 0.7713 77.13%
CYP3A4 inhibition + 0.5823 58.23%
CYP2C9 inhibition - 0.8568 85.68%
CYP2C19 inhibition - 0.7458 74.58%
CYP2D6 inhibition - 0.7790 77.90%
CYP1A2 inhibition - 0.9406 94.06%
CYP2C8 inhibition + 0.6851 68.51%
CYP inhibitory promiscuity - 0.7810 78.10%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6140 61.40%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9226 92.26%
Skin irritation - 0.8320 83.20%
Skin corrosion - 0.9500 95.00%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4356 43.56%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8795 87.95%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.9218 92.18%
Acute Oral Toxicity (c) III 0.7027 70.27%
Estrogen receptor binding + 0.7605 76.05%
Androgen receptor binding + 0.7551 75.51%
Thyroid receptor binding + 0.5368 53.68%
Glucocorticoid receptor binding + 0.6559 65.59%
Aromatase binding + 0.6970 69.70%
PPAR gamma + 0.6247 62.47%
Honey bee toxicity - 0.8790 87.90%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6104 61.04%
Fish aquatic toxicity - 0.4583 45.83%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.44% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.81% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.45% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.13% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.65% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.90% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.71% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.90% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.61% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.13% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.90% 92.62%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.49% 90.71%
CHEMBL2413 P32246 C-C chemokine receptor type 1 85.22% 89.50%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 84.50% 90.24%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.83% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.72% 95.56%
CHEMBL5028 O14672 ADAM10 80.22% 97.50%

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.
Aspidosperma desmanthum
Aspidosperma megalocarpon

Cross-Links

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PubChem 586857
LOTUS LTS0116301
wikiData Q103816803