4,5,16-Trimethoxy-11-methyl-11-azatetracyclo[8.7.1.02,7.014,18]octadeca-1(18),2,4,6,14,16-hexaene-3,17-diol

Details

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Internal ID 12121cb4-d6be-4320-b819-5e82c40a4f88
Taxonomy Alkaloids and derivatives > Homoaporphines
IUPAC Name 4,5,16-trimethoxy-11-methyl-11-azatetracyclo[8.7.1.02,7.014,18]octadeca-1(18),2,4,6,14,16-hexaene-3,17-diol
SMILES (Canonical) CN1CCC2=CC(=C(C3=C2C1CCC4=CC(=C(C(=C43)O)OC)OC)O)OC
SMILES (Isomeric) CN1CCC2=CC(=C(C3=C2C1CCC4=CC(=C(C(=C43)O)OC)OC)O)OC
InChI InChI=1S/C21H25NO5/c1-22-8-7-12-9-14(25-2)19(23)18-16(12)13(22)6-5-11-10-15(26-3)21(27-4)20(24)17(11)18/h9-10,13,23-24H,5-8H2,1-4H3
InChI Key KSXDNYMXILTIFF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H25NO5
Molecular Weight 371.40 g/mol
Exact Mass 371.17327290 g/mol
Topological Polar Surface Area (TPSA) 71.40 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.27
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,5,16-Trimethoxy-11-methyl-11-azatetracyclo[8.7.1.02,7.014,18]octadeca-1(18),2,4,6,14,16-hexaene-3,17-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7484 74.84%
Caco-2 + 0.8154 81.54%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.4537 45.37%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.9219 92.19%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.4889 48.89%
P-glycoprotein inhibitior - 0.8059 80.59%
P-glycoprotein substrate - 0.5727 57.27%
CYP3A4 substrate + 0.6121 61.21%
CYP2C9 substrate + 0.7825 78.25%
CYP2D6 substrate + 0.8432 84.32%
CYP3A4 inhibition - 0.8863 88.63%
CYP2C9 inhibition - 0.9284 92.84%
CYP2C19 inhibition - 0.8895 88.95%
CYP2D6 inhibition + 0.5673 56.73%
CYP1A2 inhibition + 0.6903 69.03%
CYP2C8 inhibition - 0.5842 58.42%
CYP inhibitory promiscuity - 0.9572 95.72%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6949 69.49%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.9388 93.88%
Skin irritation - 0.7749 77.49%
Skin corrosion - 0.9342 93.42%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6452 64.52%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.8842 88.42%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.8863 88.63%
Acute Oral Toxicity (c) III 0.6174 61.74%
Estrogen receptor binding + 0.6732 67.32%
Androgen receptor binding + 0.5447 54.47%
Thyroid receptor binding + 0.6832 68.32%
Glucocorticoid receptor binding + 0.8489 84.89%
Aromatase binding + 0.5812 58.12%
PPAR gamma + 0.6896 68.96%
Honey bee toxicity - 0.8929 89.29%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9049 90.49%

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 98.97% 96.09%
CHEMBL217 P14416 Dopamine D2 receptor 96.18% 95.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.71% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.33% 85.14%
CHEMBL2056 P21728 Dopamine D1 receptor 91.61% 91.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 91.58% 95.89%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 90.33% 91.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.85% 95.56%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 89.72% 91.79%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.23% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.92% 95.89%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 86.60% 95.34%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.36% 93.40%
CHEMBL4208 P20618 Proteasome component C5 85.35% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.62% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.18% 93.99%
CHEMBL5203 P33316 dUTP pyrophosphatase 83.87% 99.18%
CHEMBL3438 Q05513 Protein kinase C zeta 81.89% 88.48%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 81.86% 96.86%
CHEMBL2581 P07339 Cathepsin D 81.73% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.59% 92.62%
CHEMBL3820 P35557 Hexokinase type IV 81.42% 91.96%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 80.88% 95.78%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.73% 89.00%

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.
Colchicum robustum
Gloriosa superba

Cross-Links

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PubChem 11810804
LOTUS LTS0265904
wikiData Q105145628