6,7,20,21-Tetramethoxy-4,13,13,18-tetramethyl-15-(2-methylprop-1-enyl)-12,26-dioxa-4,18-diazahexacyclo[12.12.0.02,11.05,10.016,25.019,24]hexacosa-2(11),5(10),6,8,16(25),19(24),20,22-octaene-3,17-dione

Details

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Internal ID 528f49f1-94cd-4724-93e1-5f56d935a24a
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Pyranoquinolines
IUPAC Name 6,7,20,21-tetramethoxy-4,13,13,18-tetramethyl-15-(2-methylprop-1-enyl)-12,26-dioxa-4,18-diazahexacyclo[12.12.0.02,11.05,10.016,25.019,24]hexacosa-2(11),5(10),6,8,16(25),19(24),20,22-octaene-3,17-dione
SMILES (Canonical) CC(=CC1C2C(C3=C(C4=C(C(=C(C=C4)OC)OC)N(C3=O)C)OC2(C)C)OC5=C1C(=O)N(C6=C5C=CC(=C6OC)OC)C)C
SMILES (Isomeric) CC(=CC1C2C(C3=C(C4=C(C(=C(C=C4)OC)OC)N(C3=O)C)OC2(C)C)OC5=C1C(=O)N(C6=C5C=CC(=C6OC)OC)C)C
InChI InChI=1S/C34H38N2O8/c1-16(2)15-19-22-27(17-11-13-20(39-7)29(41-9)25(17)35(5)32(22)37)43-31-23-28(44-34(3,4)24(19)31)18-12-14-21(40-8)30(42-10)26(18)36(6)33(23)38/h11-15,19,24,31H,1-10H3
InChI Key ATQCOFJCMNUDIH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H38N2O8
Molecular Weight 602.70 g/mol
Exact Mass 602.26281617 g/mol
Topological Polar Surface Area (TPSA) 96.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 5.40
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6,7,20,21-Tetramethoxy-4,13,13,18-tetramethyl-15-(2-methylprop-1-enyl)-12,26-dioxa-4,18-diazahexacyclo[12.12.0.02,11.05,10.016,25.019,24]hexacosa-2(11),5(10),6,8,16(25),19(24),20,22-octaene-3,17-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9492 94.92%
Caco-2 - 0.7254 72.54%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.5399 53.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8657 86.57%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9768 97.68%
P-glycoprotein inhibitior + 0.8911 89.11%
P-glycoprotein substrate - 0.6517 65.17%
CYP3A4 substrate + 0.6778 67.78%
CYP2C9 substrate - 0.7929 79.29%
CYP2D6 substrate - 0.8531 85.31%
CYP3A4 inhibition - 0.5278 52.78%
CYP2C9 inhibition - 0.5859 58.59%
CYP2C19 inhibition - 0.6570 65.70%
CYP2D6 inhibition - 0.9157 91.57%
CYP1A2 inhibition + 0.5824 58.24%
CYP2C8 inhibition - 0.5952 59.52%
CYP inhibitory promiscuity + 0.5628 56.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4345 43.45%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.8606 86.06%
Skin irritation - 0.8237 82.37%
Skin corrosion - 0.9461 94.61%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8376 83.76%
Micronuclear + 0.7400 74.00%
Hepatotoxicity - 0.5634 56.34%
skin sensitisation - 0.8884 88.84%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.4612 46.12%
Acute Oral Toxicity (c) III 0.6281 62.81%
Estrogen receptor binding + 0.8664 86.64%
Androgen receptor binding + 0.7566 75.66%
Thyroid receptor binding + 0.7222 72.22%
Glucocorticoid receptor binding + 0.8358 83.58%
Aromatase binding + 0.6548 65.48%
PPAR gamma + 0.7982 79.82%
Honey bee toxicity - 0.7041 70.41%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.8783 87.83%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.57% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.10% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.31% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.74% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.22% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.02% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.72% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.97% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.94% 86.33%
CHEMBL2581 P07339 Cathepsin D 87.26% 98.95%
CHEMBL1871 P10275 Androgen Receptor 86.94% 96.43%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.48% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.43% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.32% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.88% 82.38%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.45% 96.00%

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.
Vepris soyauxii

Cross-Links

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PubChem 102146899
LOTUS LTS0041993
wikiData Q104918594