Tephrowatsin C

Details

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Internal ID 5a0f5220-d9d0-470e-9906-2809456fb1e8
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name 5-hydroxy-8-(3-hydroxy-3-methylbutyl)-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H24O5/c1-21(2,24)10-9-14-18(25-3)12-16(23)19-15(22)11-17(26-20(14)19)13-7-5-4-6-8-13/h4-8,12,17,23-24H,9-11H2,1-3H3
InChI Key OHGGGSHTYPJICB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H24O5
Molecular Weight 356.40 g/mol
Exact Mass 356.16237386 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.81
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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CHEBI:168000
LMPK12140175
5-hydroxy-8-(3-hydroxy-3-methylbutyl)-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one

2D Structure

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2D Structure of Tephrowatsin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9844 98.44%
Caco-2 + 0.8025 80.25%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8225 82.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8695 86.95%
OATP1B3 inhibitior + 0.9042 90.42%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5880 58.80%
P-glycoprotein inhibitior - 0.4409 44.09%
P-glycoprotein substrate - 0.7742 77.42%
CYP3A4 substrate + 0.5771 57.71%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7943 79.43%
CYP3A4 inhibition - 0.6788 67.88%
CYP2C9 inhibition - 0.6624 66.24%
CYP2C19 inhibition - 0.7537 75.37%
CYP2D6 inhibition - 0.8874 88.74%
CYP1A2 inhibition + 0.5928 59.28%
CYP2C8 inhibition + 0.6726 67.26%
CYP inhibitory promiscuity - 0.7137 71.37%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6674 66.74%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.7460 74.60%
Skin irritation - 0.7724 77.24%
Skin corrosion - 0.9414 94.14%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4899 48.99%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.6051 60.51%
skin sensitisation - 0.8941 89.41%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6668 66.68%
Acute Oral Toxicity (c) III 0.4837 48.37%
Estrogen receptor binding + 0.7054 70.54%
Androgen receptor binding + 0.5815 58.15%
Thyroid receptor binding + 0.5612 56.12%
Glucocorticoid receptor binding + 0.7603 76.03%
Aromatase binding - 0.5087 50.87%
PPAR gamma + 0.8373 83.73%
Honey bee toxicity - 0.8073 80.73%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5351 53.51%
Fish aquatic toxicity + 0.9494 94.94%

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 99.05% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.16% 86.33%
CHEMBL2581 P07339 Cathepsin D 95.84% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.82% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.08% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.52% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.90% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.83% 85.14%
CHEMBL2535 P11166 Glucose transporter 86.76% 98.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.53% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.71% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.47% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.32% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.23% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 82.47% 94.73%
CHEMBL4208 P20618 Proteasome component C5 80.21% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.08% 92.62%

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.
Tephrosia watsoniana

Cross-Links

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PubChem 42607874
LOTUS LTS0009301
wikiData Q105192064