Fluostatin L

Details

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Internal ID 5cf146c9-cee5-4e99-aa8a-3df73b5c32c8
Taxonomy Benzenoids > Fluorenes
IUPAC Name [(3R,4S,6S)-10,13-dihydroxy-6-methyl-7,18-dioxo-5-oxapentacyclo[9.7.0.02,8.04,6.012,17]octadeca-1,8,10,12(17),13,15-hexaen-3-yl] 4-methylhexanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H24O7/c1-4-11(2)8-9-16(28)31-22-18-13(23(30)25(3)24(22)32-25)10-15(27)19-17-12(21(29)20(18)19)6-5-7-14(17)26/h5-7,10-11,22,24,26-27H,4,8-9H2,1-3H3/t11?,22-,24+,25-/m1/s1
InChI Key YQMGQEJXXQCDAU-SNVRGYBNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H24O7
Molecular Weight 436.50 g/mol
Exact Mass 436.15220310 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.07
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Fluostatin L

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9757 97.57%
Caco-2 - 0.6724 67.24%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6632 66.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8475 84.75%
OATP1B3 inhibitior + 0.8088 80.88%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8754 87.54%
P-glycoprotein inhibitior + 0.6044 60.44%
P-glycoprotein substrate + 0.6598 65.98%
CYP3A4 substrate + 0.6514 65.14%
CYP2C9 substrate + 0.5851 58.51%
CYP2D6 substrate - 0.8560 85.60%
CYP3A4 inhibition - 0.8346 83.46%
CYP2C9 inhibition - 0.7013 70.13%
CYP2C19 inhibition - 0.7606 76.06%
CYP2D6 inhibition - 0.9293 92.93%
CYP1A2 inhibition - 0.6556 65.56%
CYP2C8 inhibition + 0.4915 49.15%
CYP inhibitory promiscuity - 0.8255 82.55%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6261 62.61%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.8574 85.74%
Skin irritation - 0.7134 71.34%
Skin corrosion - 0.9250 92.50%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7044 70.44%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.5462 54.62%
skin sensitisation - 0.8739 87.39%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.6261 62.61%
Acute Oral Toxicity (c) III 0.4493 44.93%
Estrogen receptor binding + 0.7252 72.52%
Androgen receptor binding + 0.6747 67.47%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7608 76.08%
Aromatase binding - 0.5586 55.86%
PPAR gamma + 0.7707 77.07%
Honey bee toxicity - 0.7706 77.06%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9972 99.72%

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
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 98.43% 96.38%
CHEMBL2581 P07339 Cathepsin D 98.30% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.87% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 96.19% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.84% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.96% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.35% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.30% 89.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.17% 93.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.17% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 90.57% 89.63%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.85% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 88.29% 91.19%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.23% 94.45%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.46% 93.03%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.29% 96.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.20% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.08% 99.17%
CHEMBL1937 Q92769 Histone deacetylase 2 84.71% 94.75%
CHEMBL2535 P11166 Glucose transporter 83.66% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.87% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.39% 96.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.47% 90.71%

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 122367507
LOTUS LTS0229293
wikiData Q77573498