Chaetospirolactone

Details

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Internal ID a7fa5db8-8293-4259-96b0-b8732108b19a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha-acyloxy carbonyl compounds > Alpha-acyloxy ketones
IUPAC Name (3R,5R)-3-hydroxy-7,8-bis[(E)-prop-1-enyl]-1-oxaspiro[4.4]non-7-ene-2,9-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H16O4/c1-3-5-9-7-14(8-11(15)13(17)18-14)12(16)10(9)6-4-2/h3-6,11,15H,7-8H2,1-2H3/b5-3+,6-4+/t11-,14-/m1/s1
InChI Key XEMRXEYFLUVEGM-AIUSXAPHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O4
Molecular Weight 248.27 g/mol
Exact Mass 248.10485899 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.45
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Chaetospirolactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9354 93.54%
Caco-2 - 0.6067 60.67%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6502 65.02%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior + 0.8964 89.64%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8584 85.84%
P-glycoprotein inhibitior - 0.9668 96.68%
P-glycoprotein substrate - 0.8126 81.26%
CYP3A4 substrate + 0.5182 51.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8836 88.36%
CYP3A4 inhibition - 0.9093 90.93%
CYP2C9 inhibition - 0.9308 93.08%
CYP2C19 inhibition - 0.9135 91.35%
CYP2D6 inhibition - 0.9566 95.66%
CYP1A2 inhibition - 0.8881 88.81%
CYP2C8 inhibition - 0.9249 92.49%
CYP inhibitory promiscuity - 0.9597 95.97%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4011 40.11%
Eye corrosion - 0.9520 95.20%
Eye irritation - 0.8409 84.09%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.7595 75.95%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7540 75.40%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5210 52.10%
skin sensitisation - 0.6977 69.77%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.7488 74.88%
Acute Oral Toxicity (c) III 0.4641 46.41%
Estrogen receptor binding - 0.8197 81.97%
Androgen receptor binding + 0.5644 56.44%
Thyroid receptor binding - 0.8521 85.21%
Glucocorticoid receptor binding - 0.5884 58.84%
Aromatase binding - 0.7919 79.19%
PPAR gamma - 0.7238 72.38%
Honey bee toxicity - 0.8029 80.29%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.6463 64.63%

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 95.20% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.18% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.42% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.82% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.00% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.64% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.68% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.12% 85.14%
CHEMBL2581 P07339 Cathepsin D 82.74% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.47% 100.00%

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.
There are no matching plants.

Cross-Links

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PubChem 139591367
LOTUS LTS0105665
wikiData Q105326440