Ponapensin

Details

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Internal ID 4ad6a290-91bb-450a-bcc4-51a31b7b2f11
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name [(1R,9R,10S,11R,12S)-1,12-dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-11-yl]-[(2S)-2-methoxypyrrolidin-1-yl]methanone
SMILES (Canonical) COC1CCCN1C(=O)C2C(C3(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C5=CC=C(C=C5)OC)C6=CC=CC=C6
SMILES (Isomeric) CO[C@H]1CCCN1C(=O)[C@@H]2[C@H]([C@]3([C@H]([C@@]2(C4=C(O3)C=C(C=C4OC)OC)O)O)C5=CC=C(C=C5)OC)C6=CC=CC=C6
InChI InChI=1S/C32H35NO8/c1-37-21-14-12-20(13-15-21)32-26(19-9-6-5-7-10-19)28(29(34)33-16-8-11-25(33)40-4)31(36,30(32)35)27-23(39-3)17-22(38-2)18-24(27)41-32/h5-7,9-10,12-15,17-18,25-26,28,30,35-36H,8,11,16H2,1-4H3/t25-,26+,28-,30-,31-,32-/m0/s1
InChI Key OLDQJFAOLFTZIG-QEQDXXSVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C32H35NO8
Molecular Weight 561.60 g/mol
Exact Mass 561.23626707 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.56
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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CHEMBL396241
CCG-261720

2D Structure

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2D Structure of Ponapensin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7759 77.59%
Caco-2 - 0.6562 65.62%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.6077 60.77%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.8739 87.39%
OATP1B3 inhibitior + 0.9428 94.28%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9575 95.75%
P-glycoprotein inhibitior + 0.8858 88.58%
P-glycoprotein substrate - 0.5716 57.16%
CYP3A4 substrate + 0.6909 69.09%
CYP2C9 substrate - 0.5833 58.33%
CYP2D6 substrate - 0.7795 77.95%
CYP3A4 inhibition - 0.8290 82.90%
CYP2C9 inhibition - 0.8413 84.13%
CYP2C19 inhibition - 0.7967 79.67%
CYP2D6 inhibition - 0.8521 85.21%
CYP1A2 inhibition - 0.8439 84.39%
CYP2C8 inhibition + 0.6991 69.91%
CYP inhibitory promiscuity - 0.9517 95.17%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6154 61.54%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9374 93.74%
Skin irritation - 0.8089 80.89%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis - 0.7070 70.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5633 56.33%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.5219 52.19%
skin sensitisation - 0.8770 87.70%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.4648 46.48%
Acute Oral Toxicity (c) III 0.5779 57.79%
Estrogen receptor binding + 0.5946 59.46%
Androgen receptor binding + 0.7998 79.98%
Thyroid receptor binding + 0.5564 55.64%
Glucocorticoid receptor binding + 0.7751 77.51%
Aromatase binding + 0.5505 55.05%
PPAR gamma + 0.5535 55.35%
Honey bee toxicity - 0.8770 87.70%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.8056 80.56%

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 98.54% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.74% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.66% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.43% 93.99%
CHEMBL5203 P33316 dUTP pyrophosphatase 95.76% 99.18%
CHEMBL2581 P07339 Cathepsin D 95.44% 98.95%
CHEMBL4208 P20618 Proteasome component C5 94.20% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 94.02% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.35% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 90.63% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 88.56% 91.19%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.09% 85.14%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.95% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.61% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.18% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.94% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.70% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.82% 94.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.79% 93.00%
CHEMBL240 Q12809 HERG 84.03% 89.76%
CHEMBL1902 P62942 FK506-binding protein 1A 83.89% 97.05%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 83.80% 100.00%
CHEMBL5028 O14672 ADAM10 82.57% 97.50%
CHEMBL1907599 P05556 Integrin alpha-4/beta-1 82.52% 92.86%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.06% 96.00%
CHEMBL221 P23219 Cyclooxygenase-1 80.89% 90.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.75% 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.
Aglaia mariannensis
Carallia brachiata
Cistus × incanus
Erythroxylum novogranatense
Excoecaria agallocha
Koompassia malaccensis
Osyris alba
Quercus glauca
Quercus miyagii
Rhizophora stylosa

Cross-Links

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PubChem 44430502
LOTUS LTS0059499
wikiData Q105203426