Palmaerone A

Details

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Internal ID def94aae-91ef-4b55-98ea-dd59f94a91fd
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3R)-5-bromo-6-hydroxy-8-methoxy-3-methyl-3,4-dihydroisochromen-1-one
SMILES (Canonical) CC1CC2=C(C(=CC(=C2C(=O)O1)OC)O)Br
SMILES (Isomeric) C[C@@H]1CC2=C(C(=CC(=C2C(=O)O1)OC)O)Br
InChI InChI=1S/C11H11BrO4/c1-5-3-6-9(11(14)16-5)8(15-2)4-7(13)10(6)12/h4-5,13H,3H2,1-2H3/t5-/m1/s1
InChI Key YICQHMNUPQNDHP-RXMQYKEDSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H11BrO4
Molecular Weight 287.11 g/mol
Exact Mass 285.98407 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Palmaerone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9690 96.90%
Caco-2 + 0.7255 72.55%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.6227 62.27%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9194 91.94%
OATP1B3 inhibitior + 0.9649 96.49%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9514 95.14%
P-glycoprotein inhibitior - 0.9316 93.16%
P-glycoprotein substrate - 0.9067 90.67%
CYP3A4 substrate + 0.5071 50.71%
CYP2C9 substrate - 0.5871 58.71%
CYP2D6 substrate - 0.8122 81.22%
CYP3A4 inhibition + 0.5255 52.55%
CYP2C9 inhibition + 0.6654 66.54%
CYP2C19 inhibition - 0.7314 73.14%
CYP2D6 inhibition - 0.7473 74.73%
CYP1A2 inhibition - 0.5343 53.43%
CYP2C8 inhibition - 0.7710 77.10%
CYP inhibitory promiscuity - 0.5669 56.69%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8449 84.49%
Carcinogenicity (trinary) Danger 0.4828 48.28%
Eye corrosion - 0.9537 95.37%
Eye irritation + 0.9039 90.39%
Skin irritation - 0.7171 71.71%
Skin corrosion - 0.9653 96.53%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6200 62.00%
Micronuclear + 0.6348 63.48%
Hepatotoxicity + 0.6803 68.03%
skin sensitisation - 0.8751 87.51%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6179 61.79%
Acute Oral Toxicity (c) II 0.4117 41.17%
Estrogen receptor binding + 0.7140 71.40%
Androgen receptor binding - 0.5285 52.85%
Thyroid receptor binding - 0.6120 61.20%
Glucocorticoid receptor binding + 0.5469 54.69%
Aromatase binding - 0.7809 78.09%
PPAR gamma - 0.5697 56.97%
Honey bee toxicity - 0.8712 87.12%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9622 96.22%

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 98.49% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.40% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.06% 86.33%
CHEMBL2535 P11166 Glucose transporter 90.93% 98.75%
CHEMBL2581 P07339 Cathepsin D 89.91% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.61% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.78% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.65% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.51% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.20% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.20% 93.99%
CHEMBL4208 P20618 Proteasome component C5 82.89% 90.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.68% 93.40%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.07% 99.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.06% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.05% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.03% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.20% 85.14%

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.
There are no matching plants.

Cross-Links

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PubChem 139590923
LOTUS LTS0244238
wikiData Q105348761