Meliatoosenin P

Details

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Internal ID f500fb86-c7bb-4dda-bfa0-27fea856492a
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name [(1R,2S,4R,5R,9R,10R,11R,12S,14R,15R,18R)-5-(furan-3-yl)-14-hydroxy-7,9,11,15-tetramethyl-10-(2-oxoethyl)-3,17-dioxapentacyclo[9.6.1.02,9.04,8.015,18]octadec-7-en-12-yl] (E)-2-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H40O7/c1-7-16(2)28(34)37-22-13-21(33)29(4)15-36-25-26(29)30(22,5)20(8-10-32)31(6)23-17(3)12-19(18-9-11-35-14-18)24(23)38-27(25)31/h7,9-11,14,19-22,24-27,33H,8,12-13,15H2,1-6H3/b16-7+/t19-,20-,21-,22+,24-,25-,26+,27-,29-,30+,31-/m1/s1
InChI Key DKAIPRHRXZMLHA-ZEVDDQGFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H40O7
Molecular Weight 524.60 g/mol
Exact Mass 524.27740361 g/mol
Topological Polar Surface Area (TPSA) 95.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 4.75
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Meliatoosenin P

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 - 0.6829 68.29%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8206 82.06%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.7302 73.02%
OATP1B3 inhibitior + 0.8275 82.75%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8114 81.14%
BSEP inhibitior + 0.9913 99.13%
P-glycoprotein inhibitior + 0.7606 76.06%
P-glycoprotein substrate + 0.6874 68.74%
CYP3A4 substrate + 0.7231 72.31%
CYP2C9 substrate - 0.7962 79.62%
CYP2D6 substrate - 0.8787 87.87%
CYP3A4 inhibition + 0.5456 54.56%
CYP2C9 inhibition - 0.6767 67.67%
CYP2C19 inhibition - 0.8779 87.79%
CYP2D6 inhibition - 0.9551 95.51%
CYP1A2 inhibition - 0.8855 88.55%
CYP2C8 inhibition + 0.7689 76.89%
CYP inhibitory promiscuity - 0.8089 80.89%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4544 45.44%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9328 93.28%
Skin irritation - 0.5781 57.81%
Skin corrosion - 0.9510 95.10%
Ames mutagenesis - 0.5064 50.64%
Human Ether-a-go-go-Related Gene inhibition + 0.8082 80.82%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.5668 56.68%
skin sensitisation - 0.8705 87.05%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5584 55.84%
Acute Oral Toxicity (c) I 0.6907 69.07%
Estrogen receptor binding + 0.7889 78.89%
Androgen receptor binding + 0.6591 65.91%
Thyroid receptor binding + 0.5780 57.80%
Glucocorticoid receptor binding + 0.8065 80.65%
Aromatase binding + 0.7175 71.75%
PPAR gamma + 0.7441 74.41%
Honey bee toxicity - 0.6544 65.44%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.68% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.20% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.33% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.19% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.52% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.78% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.74% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 92.67% 90.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.87% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 89.07% 94.73%
CHEMBL5028 O14672 ADAM10 87.58% 97.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.41% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.70% 94.00%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 83.38% 89.44%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.26% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.95% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.42% 95.50%

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.
Melia azedarach

Cross-Links

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PubChem 56950634
NPASS NPC44369