3alpha-Methoxy-3beta-deshydroxy-iso-seco-tanapartholide

Details

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Internal ID 990642a6-5569-49a4-b72e-750583ca17b7
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (4S,5S)-5-[(3R)-3-methoxy-2-methyl-5-oxocyclopenten-1-yl]-3-methylidene-4-(3-oxobutyl)oxolan-2-one
SMILES (Canonical) CC1=C(C(=O)CC1OC)C2C(C(=C)C(=O)O2)CCC(=O)C
SMILES (Isomeric) CC1=C(C(=O)C[C@H]1OC)[C@@H]2[C@H](C(=C)C(=O)O2)CCC(=O)C
InChI InChI=1S/C16H20O5/c1-8(17)5-6-11-9(2)16(19)21-15(11)14-10(3)13(20-4)7-12(14)18/h11,13,15H,2,5-7H2,1,3-4H3/t11-,13+,15-/m0/s1
InChI Key YMBVLYVGHGDKHO-LNSITVRQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O5
Molecular Weight 292.33 g/mol
Exact Mass 292.13107373 g/mol
Topological Polar Surface Area (TPSA) 69.70 Ų
XlogP 0.00
Atomic LogP (AlogP) 1.76
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3alpha-Methoxy-3beta-deshydroxy-iso-seco-tanapartholide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9809 98.09%
Caco-2 + 0.6477 64.77%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6635 66.35%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9059 90.59%
OATP1B3 inhibitior + 0.8540 85.40%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8597 85.97%
P-glycoprotein inhibitior - 0.6449 64.49%
P-glycoprotein substrate - 0.8196 81.96%
CYP3A4 substrate + 0.5479 54.79%
CYP2C9 substrate - 0.8108 81.08%
CYP2D6 substrate - 0.9029 90.29%
CYP3A4 inhibition - 0.7596 75.96%
CYP2C9 inhibition - 0.8429 84.29%
CYP2C19 inhibition - 0.7251 72.51%
CYP2D6 inhibition - 0.9402 94.02%
CYP1A2 inhibition - 0.5929 59.29%
CYP2C8 inhibition - 0.8435 84.35%
CYP inhibitory promiscuity - 0.7461 74.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8628 86.28%
Carcinogenicity (trinary) Non-required 0.6423 64.23%
Eye corrosion - 0.9528 95.28%
Eye irritation - 0.4795 47.95%
Skin irritation - 0.6332 63.32%
Skin corrosion - 0.9417 94.17%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6076 60.76%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6834 68.34%
skin sensitisation - 0.8306 83.06%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5984 59.84%
Acute Oral Toxicity (c) III 0.6169 61.69%
Estrogen receptor binding - 0.5955 59.55%
Androgen receptor binding + 0.5567 55.67%
Thyroid receptor binding - 0.7364 73.64%
Glucocorticoid receptor binding + 0.5514 55.14%
Aromatase binding - 0.7162 71.62%
PPAR gamma - 0.5391 53.91%
Honey bee toxicity - 0.6619 66.19%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9540 95.40%

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 95.77% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.45% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.20% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.09% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.98% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.52% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.33% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.17% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.36% 94.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.19% 96.09%

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 rutifolia
Azolla pinnata subsp. asiatica
Cyperus haspan
Goniothalamus thwaitesii

Cross-Links

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PubChem 101609003
NPASS NPC41587
LOTUS LTS0032273
wikiData Q105350446