Seco-Chaetomugilin A

Details

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Internal ID 836e167a-9027-4acc-8fbd-123c183a644f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name methyl (6aS,8R,9R,9aS)-5-chloro-8-hydroxy-8-[(2R,3R)-3-hydroxybutan-2-yl]-3-[(E,3R,4R)-4-hydroxy-3-methylpent-1-enyl]-6a-methyl-6-oxo-9,9a-dihydrofuro[2,3-h]isochromene-9-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H31ClO8/c1-11(13(3)26)7-8-15-9-16-17(10-32-15)18-19(22(29)31-6)24(30,12(2)14(4)27)33-23(18,5)21(28)20(16)25/h7-14,18-19,26-27,30H,1-6H3/b8-7+/t11-,12-,13-,14-,18-,19+,23+,24-/m1/s1
InChI Key FROQHXMNGOHAAZ-NCCWVHROSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C24H31ClO8
Molecular Weight 482.90 g/mol
Exact Mass 482.1707456 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.33
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Seco-Chaetomugilin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9665 96.65%
Caco-2 - 0.6054 60.54%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6634 66.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8191 81.91%
OATP1B3 inhibitior + 0.8882 88.82%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8036 80.36%
P-glycoprotein inhibitior - 0.4515 45.15%
P-glycoprotein substrate - 0.6382 63.82%
CYP3A4 substrate + 0.7068 70.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8922 89.22%
CYP3A4 inhibition - 0.7978 79.78%
CYP2C9 inhibition - 0.8060 80.60%
CYP2C19 inhibition - 0.8091 80.91%
CYP2D6 inhibition - 0.8872 88.72%
CYP1A2 inhibition - 0.8664 86.64%
CYP2C8 inhibition + 0.5980 59.80%
CYP inhibitory promiscuity + 0.5128 51.28%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8719 87.19%
Carcinogenicity (trinary) Danger 0.8329 83.29%
Eye corrosion - 0.9803 98.03%
Eye irritation - 0.9513 95.13%
Skin irritation - 0.6367 63.67%
Skin corrosion - 0.9186 91.86%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5872 58.72%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.7943 79.43%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.7507 75.07%
Acute Oral Toxicity (c) III 0.4687 46.87%
Estrogen receptor binding + 0.7606 76.06%
Androgen receptor binding + 0.7247 72.47%
Thyroid receptor binding + 0.6663 66.63%
Glucocorticoid receptor binding + 0.7444 74.44%
Aromatase binding + 0.6726 67.26%
PPAR gamma + 0.6515 65.15%
Honey bee toxicity - 0.6823 68.23%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5827 58.27%
Fish aquatic toxicity + 0.9468 94.68%

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 98.69% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.97% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.87% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.95% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 88.31% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.24% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.18% 97.14%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.42% 86.92%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 86.26% 92.88%
CHEMBL2179 P04062 Beta-glucocerebrosidase 85.42% 85.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.95% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.70% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 83.13% 90.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 82.82% 92.29%
CHEMBL340 P08684 Cytochrome P450 3A4 80.30% 91.19%

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 139588040
LOTUS LTS0180853
wikiData Q105000342