Lachnanthocarpone

Details

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Internal ID 00bbe2c5-44a1-4812-bb10-d5652751eb42
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 2,6-dihydroxy-9-phenylphenalen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H12O3/c20-15-9-6-12-10-16(21)19(22)18-13(7-8-14(15)17(12)18)11-4-2-1-3-5-11/h1-10,20-21H
InChI Key WROAYZGOYIUREA-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C19H12O3
Molecular Weight 288.30 g/mol
Exact Mass 288.078644241 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.31
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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2,6-Dihydroxy-9-phenyl-1H-phenalen-1-one
RefChem:924455
28241-21-6
5,6-dihydroxy-7-phenylphenalen-1-one
orb1696647
AKOS040752375
T32523

2D Structure

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2D Structure of Lachnanthocarpone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.6472 64.72%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8051 80.51%
OATP2B1 inhibitior - 0.7032 70.32%
OATP1B1 inhibitior + 0.9367 93.67%
OATP1B3 inhibitior + 0.8332 83.32%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.5553 55.53%
P-glycoprotein inhibitior - 0.8485 84.85%
P-glycoprotein substrate - 0.8794 87.94%
CYP3A4 substrate - 0.5326 53.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7901 79.01%
CYP3A4 inhibition - 0.7284 72.84%
CYP2C9 inhibition + 0.9468 94.68%
CYP2C19 inhibition + 0.6431 64.31%
CYP2D6 inhibition - 0.8555 85.55%
CYP1A2 inhibition + 0.8486 84.86%
CYP2C8 inhibition + 0.4706 47.06%
CYP inhibitory promiscuity + 0.8768 87.68%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Warning 0.4624 46.24%
Eye corrosion - 0.9902 99.02%
Eye irritation + 0.9834 98.34%
Skin irritation + 0.7443 74.43%
Skin corrosion - 0.9762 97.62%
Ames mutagenesis + 0.7382 73.82%
Human Ether-a-go-go-Related Gene inhibition - 0.8817 88.17%
Micronuclear + 0.6959 69.59%
Hepatotoxicity + 0.6553 65.53%
skin sensitisation + 0.7186 71.86%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.6281 62.81%
Acute Oral Toxicity (c) III 0.4481 44.81%
Estrogen receptor binding + 0.9140 91.40%
Androgen receptor binding + 0.9270 92.70%
Thyroid receptor binding + 0.7166 71.66%
Glucocorticoid receptor binding + 0.9730 97.30%
Aromatase binding + 0.8817 88.17%
PPAR gamma + 0.9178 91.78%
Honey bee toxicity - 0.8454 84.54%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9944 99.44%

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
CHEMBL1951 P21397 Monoamine oxidase A 99.80% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.71% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.99% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.96% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.40% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.13% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.00% 96.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.39% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.93% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 80.99% 90.17%

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.
Lachnanthes caroliniana
Wachendorfia paniculata

Cross-Links

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PubChem 137321736
LOTUS LTS0045364
wikiData Q105311439