1,9,10-Trimethoxy-2,3-methylenedioxynoraporphine

Details

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Internal ID 83c5a832-128c-43f4-abb6-033786ba7130
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 2,16,17-trimethoxy-4,6-dioxa-11-azapentacyclo[10.7.1.03,7.08,20.014,19]icosa-1,3(7),8(20),14,16,18-hexaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H21NO5/c1-22-14-7-10-6-13-16-11(4-5-21-13)18-20(26-9-25-18)19(24-3)17(16)12(10)8-15(14)23-2/h7-8,13,21H,4-6,9H2,1-3H3
InChI Key SZMVKWFJCYTPOI-UHFFFAOYSA-N
Popularity 3 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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There are no found synonyms.

2D Structure

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2D Structure of 1,9,10-Trimethoxy-2,3-methylenedioxynoraporphine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9689 96.89%
Caco-2 + 0.8839 88.39%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.3824 38.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9128 91.28%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.7983 79.83%
P-glycoprotein inhibitior - 0.4511 45.11%
P-glycoprotein substrate - 0.6000 60.00%
CYP3A4 substrate + 0.5978 59.78%
CYP2C9 substrate - 0.8281 82.81%
CYP2D6 substrate + 0.6636 66.36%
CYP3A4 inhibition + 0.6544 65.44%
CYP2C9 inhibition - 0.7626 76.26%
CYP2C19 inhibition - 0.6278 62.78%
CYP2D6 inhibition - 0.5059 50.59%
CYP1A2 inhibition + 0.7054 70.54%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.6903 69.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6123 61.23%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.8988 89.88%
Skin irritation - 0.7380 73.80%
Skin corrosion - 0.9397 93.97%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8118 81.18%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8313 83.13%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.4630 46.30%
Acute Oral Toxicity (c) III 0.4692 46.92%
Estrogen receptor binding + 0.7564 75.64%
Androgen receptor binding - 0.5462 54.62%
Thyroid receptor binding + 0.7426 74.26%
Glucocorticoid receptor binding + 0.7603 76.03%
Aromatase binding - 0.5215 52.15%
PPAR gamma + 0.7021 70.21%
Honey bee toxicity - 0.7647 76.47%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.4057 40.57%

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 94.28% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.15% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.04% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.81% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.37% 92.94%
CHEMBL2535 P11166 Glucose transporter 90.39% 98.75%
CHEMBL5747 Q92793 CREB-binding protein 89.91% 95.12%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.82% 96.77%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 89.30% 82.67%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.10% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.35% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.21% 93.99%
CHEMBL3438 Q05513 Protein kinase C zeta 86.40% 88.48%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.42% 95.56%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 85.10% 96.21%
CHEMBL4208 P20618 Proteasome component C5 84.07% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.35% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.75% 94.00%
CHEMBL213 P08588 Beta-1 adrenergic receptor 81.61% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.48% 97.25%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 81.31% 95.55%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.27% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.27% 99.17%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 80.64% 91.79%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 80.63% 96.39%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.57% 89.00%
CHEMBL2056 P21728 Dopamine D1 receptor 80.23% 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.
Thalictrum baicalense

Cross-Links

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PubChem 13647315
LOTUS LTS0108721
wikiData Q105264262