Fluostatin P

Details

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Internal ID dc2821e8-fc78-4a18-8d1d-8e7c91936bc3
Taxonomy Benzenoids > Fluorenes
IUPAC Name (1R,2S,3S,4R)-1,2,3,4,6-pentahydroxy-7-methoxy-3-methyl-2,4-dihydro-1H-benzo[a]fluoren-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H18O7/c1-19(25)17(23)8-6-9(20)13-11-7(4-3-5-10(11)26-2)15(21)14(13)12(8)16(22)18(19)24/h3-6,16-18,20,22-25H,1-2H3/t16-,17-,18+,19+/m1/s1
InChI Key ZHKQTTFILPJNLU-YRXWBPOGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O7
Molecular Weight 358.30 g/mol
Exact Mass 358.10525291 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.80
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Fluostatin P

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9756 97.56%
Caco-2 - 0.7831 78.31%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7224 72.24%
OATP2B1 inhibitior - 0.5700 57.00%
OATP1B1 inhibitior + 0.9162 91.62%
OATP1B3 inhibitior + 0.9631 96.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6268 62.68%
P-glycoprotein inhibitior - 0.8182 81.82%
P-glycoprotein substrate - 0.5603 56.03%
CYP3A4 substrate + 0.6503 65.03%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.7780 77.80%
CYP3A4 inhibition + 0.5112 51.12%
CYP2C9 inhibition - 0.8327 83.27%
CYP2C19 inhibition - 0.6671 66.71%
CYP2D6 inhibition - 0.8284 82.84%
CYP1A2 inhibition + 0.7457 74.57%
CYP2C8 inhibition + 0.4748 47.48%
CYP inhibitory promiscuity - 0.5836 58.36%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.4870 48.70%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.7002 70.02%
Skin irritation - 0.5938 59.38%
Skin corrosion - 0.8845 88.45%
Ames mutagenesis + 0.6830 68.30%
Human Ether-a-go-go-Related Gene inhibition - 0.6253 62.53%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8024 80.24%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.6949 69.49%
Acute Oral Toxicity (c) III 0.6299 62.99%
Estrogen receptor binding + 0.8229 82.29%
Androgen receptor binding + 0.6325 63.25%
Thyroid receptor binding + 0.6365 63.65%
Glucocorticoid receptor binding + 0.8247 82.47%
Aromatase binding + 0.6426 64.26%
PPAR gamma + 0.7966 79.66%
Honey bee toxicity - 0.8143 81.43%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9669 96.69%

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
CHEMBL2581 P07339 Cathepsin D 97.57% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.03% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.02% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.29% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 92.67% 94.75%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 92.44% 96.38%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.12% 86.33%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 91.52% 93.03%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.04% 82.69%
CHEMBL2535 P11166 Glucose transporter 91.03% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.18% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.05% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.83% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.28% 97.14%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.73% 96.67%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 83.29% 96.00%
CHEMBL2056 P21728 Dopamine D1 receptor 83.03% 91.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 82.99% 91.79%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.86% 92.94%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.10% 99.15%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.34% 94.03%
CHEMBL340 P08684 Cytochrome P450 3A4 81.19% 91.19%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.95% 93.99%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.10% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.03% 95.89%

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 139590587
LOTUS LTS0003194
wikiData Q105375814