(-)-Semivioxanthin

Details

Top
Internal ID c890f048-1306-4bfe-8ed0-86ee3b945694
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name (3S)-9,10-dihydroxy-7-methoxy-3-methyl-3,4-dihydrobenzo[g]isochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H14O5/c1-7-3-8-4-9-5-10(19-2)6-11(16)12(9)14(17)13(8)15(18)20-7/h4-7,16-17H,3H2,1-2H3/t7-/m0/s1
InChI Key BWNCKEBBYADFPQ-ZETCQYMHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H14O5
Molecular Weight 274.27 g/mol
Exact Mass 274.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
SCHEMBL2114985

2D Structure

Top
2D Structure of (-)-Semivioxanthin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8708 87.08%
Caco-2 + 0.7561 75.61%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6356 63.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8747 87.47%
OATP1B3 inhibitior + 0.9566 95.66%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8616 86.16%
P-glycoprotein inhibitior - 0.8655 86.55%
P-glycoprotein substrate - 0.8967 89.67%
CYP3A4 substrate + 0.5283 52.83%
CYP2C9 substrate + 0.6383 63.83%
CYP2D6 substrate - 0.8234 82.34%
CYP3A4 inhibition + 0.5780 57.80%
CYP2C9 inhibition - 0.5053 50.53%
CYP2C19 inhibition - 0.5974 59.74%
CYP2D6 inhibition + 0.5192 51.92%
CYP1A2 inhibition + 0.8030 80.30%
CYP2C8 inhibition - 0.7448 74.48%
CYP inhibitory promiscuity - 0.5473 54.73%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6380 63.80%
Eye corrosion - 0.9811 98.11%
Eye irritation + 0.6684 66.84%
Skin irritation - 0.7595 75.95%
Skin corrosion - 0.9559 95.59%
Ames mutagenesis - 0.5637 56.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6256 62.56%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.5299 52.99%
skin sensitisation - 0.9176 91.76%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.5615 56.15%
Acute Oral Toxicity (c) III 0.4298 42.98%
Estrogen receptor binding + 0.7873 78.73%
Androgen receptor binding + 0.6931 69.31%
Thyroid receptor binding + 0.5773 57.73%
Glucocorticoid receptor binding + 0.8145 81.45%
Aromatase binding + 0.5946 59.46%
PPAR gamma + 0.5637 56.37%
Honey bee toxicity - 0.8652 86.52%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.8788 87.88%

Targets

Top

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 99.42% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.82% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.94% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.55% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.64% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 90.23% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.66% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.63% 99.23%
CHEMBL2581 P07339 Cathepsin D 89.48% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.23% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.89% 99.17%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 86.57% 92.68%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.69% 92.94%
CHEMBL2535 P11166 Glucose transporter 84.44% 98.75%
CHEMBL4208 P20618 Proteasome component C5 83.14% 90.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.75% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.72% 97.09%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 82.40% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.28% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.75% 93.99%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 80.73% 80.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.28% 89.00%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 10659908
LOTUS LTS0214783
wikiData Q77509789