(1R)-6,20,25-trimethoxy-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),14,18,20,22(33),24,26,31-tridecaen-21-ol

Details

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Internal ID f3f6e089-0f63-4783-9ed6-72aa97524814
Taxonomy Lignans, neolignans and related compounds
IUPAC Name (1R)-6,20,25-trimethoxy-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),14,18,20,22(33),24,26,31-tridecaen-21-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C35H34N2O6/c1-39-28-9-6-21-15-26-25-19-31(29(40-2)17-22(25)10-12-36-26)43-35-33-23(18-32(41-3)34(35)38)11-13-37-27(33)14-20-4-7-24(8-5-20)42-30(28)16-21/h4-9,16-19,26,36,38H,10-15H2,1-3H3/t26-/m1/s1
InChI Key DPHNKDUWFLOVNQ-AREMUKBSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C35H34N2O6
Molecular Weight 578.70 g/mol
Exact Mass 578.24168681 g/mol
Topological Polar Surface Area (TPSA) 90.80 Ų
XlogP 5.30
Atomic LogP (AlogP) 6.33
H-Bond Acceptor 8
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 (1R)-6,20,25-trimethoxy-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),14,18,20,22(33),24,26,31-tridecaen-21-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7949 79.49%
Caco-2 - 0.7094 70.94%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5587 55.87%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8762 87.62%
OATP1B3 inhibitior + 0.9466 94.66%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9950 99.50%
P-glycoprotein inhibitior + 0.9400 94.00%
P-glycoprotein substrate + 0.7452 74.52%
CYP3A4 substrate + 0.6955 69.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3753 37.53%
CYP3A4 inhibition - 0.6246 62.46%
CYP2C9 inhibition - 0.9079 90.79%
CYP2C19 inhibition - 0.8125 81.25%
CYP2D6 inhibition - 0.7272 72.72%
CYP1A2 inhibition - 0.7027 70.27%
CYP2C8 inhibition + 0.7515 75.15%
CYP inhibitory promiscuity - 0.9462 94.62%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6707 67.07%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.9518 95.18%
Skin irritation - 0.7553 75.53%
Skin corrosion - 0.9315 93.15%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9057 90.57%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.8476 84.76%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.6778 67.78%
Acute Oral Toxicity (c) III 0.5483 54.83%
Estrogen receptor binding + 0.8726 87.26%
Androgen receptor binding + 0.6470 64.70%
Thyroid receptor binding + 0.7509 75.09%
Glucocorticoid receptor binding + 0.8622 86.22%
Aromatase binding + 0.6396 63.96%
PPAR gamma + 0.7253 72.53%
Honey bee toxicity - 0.7731 77.31%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5851 58.51%
Fish aquatic toxicity - 0.6537 65.37%

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 98.95% 96.09%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 97.93% 96.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.59% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.56% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 94.09% 95.89%
CHEMBL2581 P07339 Cathepsin D 92.01% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.59% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.73% 93.99%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.67% 97.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 88.75% 95.78%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.08% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.92% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.89% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.43% 94.00%
CHEMBL2535 P11166 Glucose transporter 84.71% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.20% 86.33%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 83.23% 95.64%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 82.57% 89.44%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.54% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.79% 99.23%
CHEMBL2056 P21728 Dopamine D1 receptor 80.40% 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.
Alseodaphne paludosa

Cross-Links

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PubChem 44519222
LOTUS LTS0233513
wikiData Q104986504