withalongolide F

Details

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Internal ID 0a950fe6-d94f-4996-8176-06b0af4acbba
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones
IUPAC Name (2R)-2-[(1S)-1-[(3aR,3bS,5aS,6R,8aS,8bS)-3a,5a-dimethyl-3-oxo-4,5,6,7,8,8a,8b,9-octahydro-3bH-indeno[5,4-e]inden-6-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H36O4/c1-15-13-23(31-25(30)19(15)14-28)16(2)20-8-9-21-18-7-5-17-6-10-24(29)27(17,4)22(18)11-12-26(20,21)3/h5-6,10,16,18,20-23,28H,7-9,11-14H2,1-4H3/t16-,18-,20+,21-,22-,23+,26+,27-/m0/s1
InChI Key IBYXDWNHLOGYIN-OSVRZWSTSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C27H36O4
Molecular Weight 424.60 g/mol
Exact Mass 424.26135963 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.78
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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CHEBI:69111
CHEMBL1934458
SCHEMBL11950402
DTXSID201098399
nor-27-hydroxy-1-oxowitha-2,5,24-trienolide
Q27137452
(6R)-6-[(1S)-1-[(1R,3aS,3bS,8aR,8bS,10aS)-1,2,3,3a,3b,4,8,8a,8b,9,10,10a-Dodecahydro-8a,10a-dimethyl-8-oxodicyclopenta[a,f]naphthalen-1-yl]ethyl]-5,6-dihydro-3-(hydroxymethyl)-4-methyl-2H-pyran-2-one
(6R)-6-{(1S)-1-[(1R,3aS,3bS,8aR,8bS,10aS)-8a,10a-dimethyl-8-oxo-1,2,3,3a,3b,4,8,8a,8b,9,10,10a-dodecahydrodicyclopenta[a,f]naphthalen-1-yl]ethyl}-3-(hydroxymethyl)-4-methyl-5,6-dihydro-2H-pyran-2-one
1350448-47-3

2D Structure

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2D Structure of withalongolide F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9659 96.59%
Caco-2 - 0.5253 52.53%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7950 79.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8719 87.19%
OATP1B3 inhibitior + 0.9546 95.46%
MATE1 inhibitior - 0.9212 92.12%
OCT2 inhibitior + 0.5412 54.12%
BSEP inhibitior + 0.9650 96.50%
P-glycoprotein inhibitior + 0.8143 81.43%
P-glycoprotein substrate + 0.5545 55.45%
CYP3A4 substrate + 0.7163 71.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9109 91.09%
CYP3A4 inhibition - 0.6580 65.80%
CYP2C9 inhibition - 0.9351 93.51%
CYP2C19 inhibition - 0.9531 95.31%
CYP2D6 inhibition - 0.9577 95.77%
CYP1A2 inhibition - 0.6190 61.90%
CYP2C8 inhibition + 0.4586 45.86%
CYP inhibitory promiscuity - 0.9128 91.28%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6143 61.43%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9803 98.03%
Skin irritation + 0.6583 65.83%
Skin corrosion - 0.9375 93.75%
Ames mutagenesis - 0.6614 66.14%
Human Ether-a-go-go-Related Gene inhibition + 0.7738 77.38%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5665 56.65%
skin sensitisation - 0.9053 90.53%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.4858 48.58%
Acute Oral Toxicity (c) III 0.7411 74.11%
Estrogen receptor binding + 0.8573 85.73%
Androgen receptor binding + 0.7549 75.49%
Thyroid receptor binding + 0.7203 72.03%
Glucocorticoid receptor binding + 0.8954 89.54%
Aromatase binding + 0.6672 66.72%
PPAR gamma + 0.6878 68.78%
Honey bee toxicity - 0.8359 83.59%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9781 97.81%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.29% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.25% 97.25%
CHEMBL2581 P07339 Cathepsin D 93.46% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.99% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.54% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.44% 91.11%
CHEMBL5103 Q969S8 Histone deacetylase 10 88.84% 90.08%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.48% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 87.50% 94.75%
CHEMBL3310 Q96DB2 Histone deacetylase 11 86.63% 88.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.52% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.46% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.15% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.95% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.91% 97.14%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.66% 93.04%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.43% 93.03%
CHEMBL4581 P52732 Kinesin-like protein 1 81.27% 93.18%
CHEMBL3401 O75469 Pregnane X receptor 80.67% 94.73%
CHEMBL1871 P10275 Androgen Receptor 80.61% 96.43%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.45% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.44% 94.00%

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.
Physalis longifolia

Cross-Links

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PubChem 56926117
LOTUS LTS0048932
wikiData Q27137452