Palmarumycin B6

Details

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Internal ID 1428d17d-ff7d-4604-bee6-e9d0cb8dfe68
Taxonomy Benzenoids > Tetralins
IUPAC Name 5-chloro-8-hydroxyspiro[2,3-dihydronaphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H13ClO4/c21-12-7-8-13(22)18-14(23)9-10-20(19(12)18)24-15-5-1-3-11-4-2-6-16(25-20)17(11)15/h1-8,22H,9-10H2
InChI Key YWUWMXDEUDNGHC-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H13ClO4
Molecular Weight 352.80 g/mol
Exact Mass 352.0502366 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.80
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEMBL3342637

2D Structure

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2D Structure of Palmarumycin B6

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9469 94.69%
Caco-2 + 0.7050 70.50%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6997 69.97%
OATP2B1 inhibitior - 0.8591 85.91%
OATP1B1 inhibitior + 0.9209 92.09%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8319 83.19%
P-glycoprotein inhibitior - 0.6953 69.53%
P-glycoprotein substrate - 0.9690 96.90%
CYP3A4 substrate + 0.5536 55.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8276 82.76%
CYP3A4 inhibition - 0.7929 79.29%
CYP2C9 inhibition + 0.6488 64.88%
CYP2C19 inhibition - 0.6481 64.81%
CYP2D6 inhibition - 0.8768 87.68%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.6897 68.97%
CYP inhibitory promiscuity - 0.8642 86.42%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8276 82.76%
Carcinogenicity (trinary) Danger 0.4285 42.85%
Eye corrosion - 0.9735 97.35%
Eye irritation - 0.4929 49.29%
Skin irritation - 0.6218 62.18%
Skin corrosion - 0.9481 94.81%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5836 58.36%
Micronuclear - 0.5267 52.67%
Hepatotoxicity + 0.6209 62.09%
skin sensitisation - 0.7639 76.39%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.7967 79.67%
Acute Oral Toxicity (c) I 0.4519 45.19%
Estrogen receptor binding + 0.9128 91.28%
Androgen receptor binding + 0.7162 71.62%
Thyroid receptor binding - 0.4916 49.16%
Glucocorticoid receptor binding + 0.5919 59.19%
Aromatase binding + 0.5427 54.27%
PPAR gamma + 0.9068 90.68%
Honey bee toxicity - 0.8966 89.66%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.8925 89.25%

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 99.49% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.78% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.36% 95.56%
CHEMBL240 Q12809 HERG 92.40% 89.76%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.53% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.72% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.01% 93.99%
CHEMBL2581 P07339 Cathepsin D 86.67% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.62% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 84.22% 94.75%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.09% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 83.85% 94.73%
CHEMBL4208 P20618 Proteasome component C5 82.84% 90.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.72% 96.61%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.42% 93.40%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.26% 85.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101888374
LOTUS LTS0179067
wikiData Q77377316