Isosecotanapartholide

Details

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Internal ID 47e3e72b-b44a-4c12-8728-42de282e4bd7
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (4S,5S)-5-[(3S)-3-hydroxy-2-methyl-5-oxocyclopenten-1-yl]-3-methylidene-4-(3-oxobutyl)oxolan-2-one
SMILES (Canonical) CC1=C(C(=O)CC1O)C2C(C(=C)C(=O)O2)CCC(=O)C
SMILES (Isomeric) CC1=C(C(=O)C[C@@H]1O)[C@@H]2[C@H](C(=C)C(=O)O2)CCC(=O)C
InChI InChI=1S/C15H18O5/c1-7(16)4-5-10-8(2)15(19)20-14(10)13-9(3)11(17)6-12(13)18/h10-11,14,17H,2,4-6H2,1,3H3/t10-,11-,14-/m0/s1
InChI Key XXYRTFCLQHKIDU-MJVIPROJSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O5
Molecular Weight 278.30 g/mol
Exact Mass 278.11542367 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP -0.50
Atomic LogP (AlogP) 1.10
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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CHEBI:66089
(4S,5S)-5-[(3S)-3-hydroxy-2-methyl-5-oxocyclopent-1-en-1-yl]-3-methylidene-4-(3-oxobutyl)dihydrofuran-2(3H)-one
(4S,5S)-5-[(3S)-3-hydroxy-2-methyl-5-oxocyclopenten-1-yl]-3-methylidene-4-(3-oxobutyl)oxolan-2-one
CHEMBL508537
Q27134603

2D Structure

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2D Structure of Isosecotanapartholide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9762 97.62%
Caco-2 + 0.6743 67.43%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6779 67.79%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9003 90.03%
OATP1B3 inhibitior + 0.9013 90.13%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9389 93.89%
P-glycoprotein inhibitior - 0.8453 84.53%
P-glycoprotein substrate - 0.8740 87.40%
CYP3A4 substrate - 0.5092 50.92%
CYP2C9 substrate - 0.7970 79.70%
CYP2D6 substrate - 0.8970 89.70%
CYP3A4 inhibition - 0.8228 82.28%
CYP2C9 inhibition - 0.8959 89.59%
CYP2C19 inhibition - 0.8708 87.08%
CYP2D6 inhibition - 0.9366 93.66%
CYP1A2 inhibition - 0.7372 73.72%
CYP2C8 inhibition - 0.9010 90.10%
CYP inhibitory promiscuity - 0.9403 94.03%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8928 89.28%
Carcinogenicity (trinary) Non-required 0.6380 63.80%
Eye corrosion - 0.9567 95.67%
Eye irritation + 0.7528 75.28%
Skin irritation + 0.5630 56.30%
Skin corrosion - 0.8183 81.83%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5849 58.49%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.6834 68.34%
skin sensitisation - 0.7658 76.58%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.6204 62.04%
Acute Oral Toxicity (c) III 0.5996 59.96%
Estrogen receptor binding - 0.6601 66.01%
Androgen receptor binding - 0.5303 53.03%
Thyroid receptor binding - 0.6831 68.31%
Glucocorticoid receptor binding - 0.5358 53.58%
Aromatase binding - 0.8304 83.04%
PPAR gamma - 0.6411 64.11%
Honey bee toxicity - 0.8264 82.64%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9451 94.51%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.24% 85.14%
CHEMBL2581 P07339 Cathepsin D 91.26% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.31% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.67% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.50% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.98% 95.56%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.90% 91.24%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.62% 93.03%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 81.99% 96.38%

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.
Artemisia gilvescens
Artemisia gmelinii
Artemisia rutifolia
Artemisia xanthochroa
Artemisia xerophytica
Eupatorium capillifolium
Seriphidium deserti

Cross-Links

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PubChem 13918473
NPASS NPC106510
ChEMBL CHEMBL508537
LOTUS LTS0198685
wikiData Q27134603