2,2-bis(1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl)acetaldehyde

Details

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Internal ID f37cf2ae-9ef2-417d-9838-d43d123adaf3
Taxonomy Alkaloids and derivatives > Benzophenanthridine alkaloids > Dihydrobenzophenanthridine alkaloids
IUPAC Name 2,2-bis(1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl)acetaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C44H38N2O9/c1-45-39-26(9-7-22-15-33-35(17-28(22)39)54-20-52-33)24-11-13-31(48-3)43(50-5)37(24)41(45)30(19-47)42-38-25(12-14-32(49-4)44(38)51-6)27-10-8-23-16-34-36(55-21-53-34)18-29(23)40(27)46(42)2/h7-19,30,41-42H,20-21H2,1-6H3
InChI Key YYKYNNGISDNCMR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C44H38N2O9
Molecular Weight 738.80 g/mol
Exact Mass 738.25773079 g/mol
Topological Polar Surface Area (TPSA) 97.40 Ų
XlogP 7.80
Atomic LogP (AlogP) 8.32
H-Bond Acceptor 11
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,2-bis(1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl)acetaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9020 90.20%
Caco-2 - 0.6461 64.61%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.4709 47.09%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.9088 90.88%
OATP1B3 inhibitior + 0.9456 94.56%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9909 99.09%
P-glycoprotein inhibitior + 0.9290 92.90%
P-glycoprotein substrate + 0.5350 53.50%
CYP3A4 substrate + 0.5977 59.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3694 36.94%
CYP3A4 inhibition + 0.8116 81.16%
CYP2C9 inhibition - 0.5337 53.37%
CYP2C19 inhibition + 0.8993 89.93%
CYP2D6 inhibition + 0.5976 59.76%
CYP1A2 inhibition + 0.7498 74.98%
CYP2C8 inhibition + 0.4788 47.88%
CYP inhibitory promiscuity + 0.8983 89.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4022 40.22%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9181 91.81%
Skin irritation - 0.8179 81.79%
Skin corrosion - 0.9561 95.61%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9394 93.94%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.5659 56.59%
skin sensitisation - 0.8789 87.89%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8489 84.89%
Acute Oral Toxicity (c) III 0.7258 72.58%
Estrogen receptor binding + 0.8564 85.64%
Androgen receptor binding + 0.8127 81.27%
Thyroid receptor binding + 0.6569 65.69%
Glucocorticoid receptor binding + 0.8603 86.03%
Aromatase binding + 0.5918 59.18%
PPAR gamma + 0.7500 75.00%
Honey bee toxicity - 0.7481 74.81%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8992 89.92%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.93% 96.77%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 95.22% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.55% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.08% 96.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 94.06% 92.62%
CHEMBL2581 P07339 Cathepsin D 91.93% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.21% 86.33%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 91.06% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.76% 96.00%
CHEMBL4208 P20618 Proteasome component C5 89.18% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 88.46% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.39% 89.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 88.07% 90.24%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.59% 94.00%
CHEMBL2535 P11166 Glucose transporter 85.21% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.07% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.46% 99.17%
CHEMBL5747 Q92793 CREB-binding protein 84.18% 95.12%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 83.64% 97.31%
CHEMBL1907 P15144 Aminopeptidase N 82.32% 93.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.01% 91.11%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.64% 80.78%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.06% 100.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.93% 89.50%

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.
Zanthoxylum spinosum

Cross-Links

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PubChem 13946327
LOTUS LTS0028151
wikiData Q105368709