(1S,2R,17R)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,15,19(28),20,22,24-nonaene-13,27-dione

Details

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Internal ID 42e3fdd4-1b57-49d1-a994-581d2d383e32
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Pyranoquinolines
IUPAC Name (1S,2R,17R)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,15,19(28),20,22,24-nonaene-13,27-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H28N2O4/c1-29(2)24-18(22-25(35-29)16-10-6-8-12-20(16)31(4)27(22)33)14-30(3)15-19(24)23-26(36-30)17-11-7-9-13-21(17)32(5)28(23)34/h6-14,19,24H,15H2,1-5H3/t19-,24+,30+/m1/s1
InChI Key GOMYFBXXKAFFLM-WEWKHQNJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H28N2O4
Molecular Weight 480.60 g/mol
Exact Mass 480.20490738 g/mol
Topological Polar Surface Area (TPSA) 59.10 Ų
XlogP 3.00
Atomic LogP (AlogP) 4.90
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,2R,17R)-3,3,12,17,26-pentamethyl-4,18-dioxa-12,26-diazaheptacyclo[15.11.1.02,15.05,14.06,11.019,28.020,25]nonacosa-5(14),6,8,10,15,19(28),20,22,24-nonaene-13,27-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9771 97.71%
Caco-2 - 0.5550 55.50%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6133 61.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8979 89.79%
OATP1B3 inhibitior + 0.9470 94.70%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9138 91.38%
P-glycoprotein inhibitior + 0.8427 84.27%
P-glycoprotein substrate - 0.6055 60.55%
CYP3A4 substrate + 0.7047 70.47%
CYP2C9 substrate - 0.6070 60.70%
CYP2D6 substrate - 0.8271 82.71%
CYP3A4 inhibition - 0.6456 64.56%
CYP2C9 inhibition - 0.5782 57.82%
CYP2C19 inhibition - 0.6177 61.77%
CYP2D6 inhibition - 0.8377 83.77%
CYP1A2 inhibition - 0.5331 53.31%
CYP2C8 inhibition - 0.6930 69.30%
CYP inhibitory promiscuity - 0.6605 66.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.4224 42.24%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.8748 87.48%
Skin irritation - 0.8029 80.29%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8847 88.47%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.5159 51.59%
skin sensitisation - 0.8590 85.90%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5611 56.11%
Estrogen receptor binding + 0.8820 88.20%
Androgen receptor binding + 0.7894 78.94%
Thyroid receptor binding + 0.6933 69.33%
Glucocorticoid receptor binding + 0.8495 84.95%
Aromatase binding + 0.6036 60.36%
PPAR gamma + 0.7840 78.40%
Honey bee toxicity - 0.8373 83.73%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 0.9240 92.40%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.11% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.09% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.67% 89.00%
CHEMBL255 P29275 Adenosine A2b receptor 95.48% 98.59%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.87% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.84% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.60% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 91.29% 91.49%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.23% 85.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.80% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.60% 97.25%
CHEMBL240 Q12809 HERG 85.37% 89.76%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.95% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.44% 94.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.40% 96.25%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.60% 97.14%
CHEMBL3384 Q16512 Protein kinase N1 82.05% 80.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.94% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 81.28% 94.75%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 81.26% 85.11%
CHEMBL3524 P56524 Histone deacetylase 4 80.66% 92.97%

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.
Euxylophora paraensis

Cross-Links

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PubChem 162844130
LOTUS LTS0212306
wikiData Q105014259