Cassialactone

Details

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Internal ID 52206b4f-8240-446e-a183-af04e4ebc9e6
Taxonomy Organoheterocyclic compounds > Benzoxepines
IUPAC Name 4,10,11-trihydroxy-8-methoxy-4-methyl-3,5-dihydrobenzo[h][2]benzoxepin-1-one
SMILES (Canonical) CC1(CC2=CC3=CC(=CC(=C3C(=C2C(=O)OC1)O)O)OC)O
SMILES (Isomeric) CC1(CC2=CC3=CC(=CC(=C3C(=C2C(=O)OC1)O)O)OC)O
InChI InChI=1S/C16H16O6/c1-16(20)6-9-3-8-4-10(21-2)5-11(17)12(8)14(18)13(9)15(19)22-7-16/h3-5,17-18,20H,6-7H2,1-2H3
InChI Key SOTIRKODYDVBCJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O6
Molecular Weight 304.29 g/mol
Exact Mass 304.09468823 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.72
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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SOTIRKODYDVBCJ-UHFFFAOYSA-N
4,10,11-Trihydroxy-8-methoxy-4-methyl-4,5-dihydronaphtho[2,3-c]oxepin-1(3H)-one #
80489-64-1

2D Structure

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2D Structure of Cassialactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9261 92.61%
Caco-2 + 0.8114 81.14%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5157 51.57%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8937 89.37%
OATP1B3 inhibitior + 0.9177 91.77%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7695 76.95%
P-glycoprotein inhibitior - 0.8682 86.82%
P-glycoprotein substrate - 0.7925 79.25%
CYP3A4 substrate + 0.5787 57.87%
CYP2C9 substrate + 0.6290 62.90%
CYP2D6 substrate - 0.8293 82.93%
CYP3A4 inhibition - 0.6462 64.62%
CYP2C9 inhibition - 0.7883 78.83%
CYP2C19 inhibition - 0.7858 78.58%
CYP2D6 inhibition - 0.7388 73.88%
CYP1A2 inhibition - 0.6469 64.69%
CYP2C8 inhibition - 0.6174 61.74%
CYP inhibitory promiscuity - 0.8285 82.85%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5893 58.93%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.4882 48.82%
Skin irritation - 0.7893 78.93%
Skin corrosion - 0.9464 94.64%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6725 67.25%
Micronuclear + 0.5774 57.74%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8479 84.79%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.7541 75.41%
Acute Oral Toxicity (c) III 0.5169 51.69%
Estrogen receptor binding + 0.8763 87.63%
Androgen receptor binding + 0.6902 69.02%
Thyroid receptor binding + 0.5189 51.89%
Glucocorticoid receptor binding + 0.8199 81.99%
Aromatase binding + 0.7724 77.24%
PPAR gamma + 0.8442 84.42%
Honey bee toxicity - 0.8792 87.92%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8780 87.80%

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 99.80% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.05% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.60% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.55% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.30% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.12% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.05% 94.00%
CHEMBL2581 P07339 Cathepsin D 92.99% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.10% 86.33%
CHEMBL4208 P20618 Proteasome component C5 91.04% 90.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 90.23% 91.07%
CHEMBL230 P35354 Cyclooxygenase-2 89.15% 89.63%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 88.61% 80.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.38% 99.23%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 87.89% 92.68%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.11% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 84.76% 94.75%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 83.49% 81.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.45% 92.94%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.49% 95.50%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.86% 97.36%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.85% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 80.47% 94.73%

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.
Senna obtusifolia
Senna tora

Cross-Links

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PubChem 627638
NPASS NPC182472
LOTUS LTS0172797
wikiData Q105257184