O-Methylcassyfiline

Details

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Internal ID b5b4a718-7a22-48c4-9402-5874996f1b25
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 7,16,17-trimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14,16,18-hexaene
SMILES (Canonical) COC1=C(C=C2C(=C1)CC3C4=C(CCN3)C(=C5C(=C24)OCO5)OC)OC
SMILES (Isomeric) COC1=C(C=C2C(=C1)CC3C4=C(CCN3)C(=C5C(=C24)OCO5)OC)OC
InChI InChI=1S/C20H21NO5/c1-22-14-7-10-6-13-16-11(4-5-21-13)18(24-3)20-19(25-9-26-20)17(16)12(10)8-15(14)23-2/h7-8,13,21H,4-6,9H2,1-3H3
InChI Key YYPGFVKLIUMIEL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H21NO5
Molecular Weight 355.40 g/mol
Exact Mass 355.14197277 g/mol
Topological Polar Surface Area (TPSA) 58.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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NP251

2D Structure

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2D Structure of O-Methylcassyfiline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9539 95.39%
Caco-2 + 0.9262 92.62%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.3770 37.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9167 91.67%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.7495 74.95%
P-glycoprotein inhibitior - 0.5741 57.41%
P-glycoprotein substrate - 0.5941 59.41%
CYP3A4 substrate + 0.5922 59.22%
CYP2C9 substrate - 0.8281 82.81%
CYP2D6 substrate + 0.6636 66.36%
CYP3A4 inhibition + 0.7041 70.41%
CYP2C9 inhibition - 0.7536 75.36%
CYP2C19 inhibition - 0.5714 57.14%
CYP2D6 inhibition - 0.5889 58.89%
CYP1A2 inhibition + 0.7016 70.16%
CYP2C8 inhibition - 0.5766 57.66%
CYP inhibitory promiscuity + 0.6879 68.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6100 61.00%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.8725 87.25%
Skin irritation - 0.7419 74.19%
Skin corrosion - 0.9386 93.86%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7522 75.22%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8365 83.65%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.4626 46.26%
Acute Oral Toxicity (c) III 0.4599 45.99%
Estrogen receptor binding + 0.7973 79.73%
Androgen receptor binding - 0.5462 54.62%
Thyroid receptor binding + 0.7805 78.05%
Glucocorticoid receptor binding + 0.7852 78.52%
Aromatase binding - 0.5086 50.86%
PPAR gamma + 0.6606 66.06%
Honey bee toxicity - 0.7996 79.96%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.3760 37.60%

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 96.03% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.71% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.37% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.53% 93.99%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.06% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.14% 92.94%
CHEMBL5747 Q92793 CREB-binding protein 90.90% 95.12%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 89.34% 82.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.21% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.49% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.31% 92.62%
CHEMBL261 P00915 Carbonic anhydrase I 87.19% 96.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.95% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.94% 93.40%
CHEMBL2535 P11166 Glucose transporter 86.60% 98.75%
CHEMBL2581 P07339 Cathepsin D 85.78% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.58% 90.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.44% 97.25%
CHEMBL3438 Q05513 Protein kinase C zeta 84.94% 88.48%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 83.98% 95.53%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.33% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.07% 94.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.89% 96.21%
CHEMBL2056 P21728 Dopamine D1 receptor 80.73% 91.00%

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.
Cassytha filiformis
Ocotea acutifolia
Ocotea velloziana
Thalictrum flavum

Cross-Links

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PubChem 3698033
LOTUS LTS0164316
wikiData Q104399696