Scytalol B

Details

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Internal ID 65e53cea-0f53-493d-b9c9-316281edb905
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name (3S,5R)-5,9-dihydroxy-3,7-dimethoxy-3-methyl-4,4a,5,10a-tetrahydro-1H-benzo[g]isochromen-10-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H20O6/c1-16(21-3)6-10-11(7-22-16)15(19)13-9(14(10)18)4-8(20-2)5-12(13)17/h4-5,10-11,14,17-18H,6-7H2,1-3H3/t10?,11?,14-,16-/m0/s1
InChI Key VMMAWQXIQXLFRX-GVSXRFJSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O6
Molecular Weight 308.33 g/mol
Exact Mass 308.12598835 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.65
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Scytalol B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9366 93.66%
Caco-2 + 0.7202 72.02%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7767 77.67%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8589 85.89%
OATP1B3 inhibitior + 0.9095 90.95%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7539 75.39%
P-glycoprotein inhibitior - 0.8327 83.27%
P-glycoprotein substrate - 0.7898 78.98%
CYP3A4 substrate + 0.6453 64.53%
CYP2C9 substrate - 0.8257 82.57%
CYP2D6 substrate - 0.8269 82.69%
CYP3A4 inhibition - 0.7453 74.53%
CYP2C9 inhibition - 0.7438 74.38%
CYP2C19 inhibition - 0.6957 69.57%
CYP2D6 inhibition - 0.8746 87.46%
CYP1A2 inhibition + 0.8028 80.28%
CYP2C8 inhibition + 0.4672 46.72%
CYP inhibitory promiscuity - 0.8443 84.43%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.6553 65.53%
Eye corrosion - 0.9862 98.62%
Eye irritation - 0.8886 88.86%
Skin irritation - 0.8197 81.97%
Skin corrosion - 0.9671 96.71%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7130 71.30%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.5264 52.64%
skin sensitisation - 0.8982 89.82%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5813 58.13%
Acute Oral Toxicity (c) III 0.5656 56.56%
Estrogen receptor binding + 0.8128 81.28%
Androgen receptor binding + 0.7421 74.21%
Thyroid receptor binding + 0.7052 70.52%
Glucocorticoid receptor binding + 0.8045 80.45%
Aromatase binding + 0.5511 55.11%
PPAR gamma + 0.5857 58.57%
Honey bee toxicity - 0.8055 80.55%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9572 95.72%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.26% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.20% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.40% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.46% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.70% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.16% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.09% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.21% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 89.94% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.57% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.80% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.00% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 85.61% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.41% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.01% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.89% 97.14%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.85% 92.68%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.81% 96.77%
CHEMBL4208 P20618 Proteasome component C5 84.51% 90.00%
CHEMBL2535 P11166 Glucose transporter 82.81% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.44% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.33% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.22% 99.17%
CHEMBL226 P30542 Adenosine A1 receptor 80.85% 95.93%

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 139584104
LOTUS LTS0153690
wikiData Q77279707