(2S)-2-(5-hydroxy-2-methoxyphenyl)-6-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3,4-dihydro-2H-chromen-7-ol

Details

Top
Internal ID dde1bc01-dfb3-4246-9bd6-cf946fa1d9de
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids
IUPAC Name (2S)-2-(5-hydroxy-2-methoxyphenyl)-6-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3,4-dihydro-2H-chromen-7-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H32O7/c1-37-29-14-11-23(34)16-27(29)30-13-7-21-15-26(28(36)18-32(21)39-30)25(19-3-8-22(33)9-4-19)12-6-20-5-10-24(35)17-31(20)38-2/h3-5,8-11,14-18,25,30,33-36H,6-7,12-13H2,1-2H3/t25-,30+/m1/s1
InChI Key VIRGLUVLSMUIOA-RNAHPLFWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C32H32O7
Molecular Weight 528.60 g/mol
Exact Mass 528.21480336 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.36
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2S)-2-(5-hydroxy-2-methoxyphenyl)-6-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3,4-dihydro-2H-chromen-7-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9038 90.38%
Caco-2 - 0.7481 74.81%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.8562 85.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8765 87.65%
OATP1B3 inhibitior + 0.9625 96.25%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9871 98.71%
P-glycoprotein inhibitior + 0.9002 90.02%
P-glycoprotein substrate + 0.6643 66.43%
CYP3A4 substrate + 0.6682 66.82%
CYP2C9 substrate - 0.6025 60.25%
CYP2D6 substrate + 0.5974 59.74%
CYP3A4 inhibition - 0.6502 65.02%
CYP2C9 inhibition + 0.7399 73.99%
CYP2C19 inhibition + 0.7828 78.28%
CYP2D6 inhibition - 0.6663 66.63%
CYP1A2 inhibition + 0.7542 75.42%
CYP2C8 inhibition + 0.7366 73.66%
CYP inhibitory promiscuity + 0.8656 86.56%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6381 63.81%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.8834 88.34%
Skin irritation - 0.7963 79.63%
Skin corrosion - 0.9386 93.86%
Ames mutagenesis - 0.7237 72.37%
Human Ether-a-go-go-Related Gene inhibition + 0.9546 95.46%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.9139 91.39%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8873 88.73%
Acute Oral Toxicity (c) III 0.4324 43.24%
Estrogen receptor binding + 0.8655 86.55%
Androgen receptor binding + 0.8090 80.90%
Thyroid receptor binding + 0.6946 69.46%
Glucocorticoid receptor binding + 0.8160 81.60%
Aromatase binding - 0.6090 60.90%
PPAR gamma + 0.6755 67.55%
Honey bee toxicity - 0.7236 72.36%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5049 50.49%
Fish aquatic toxicity + 0.7277 72.77%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.82% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.35% 91.11%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 96.41% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.39% 99.17%
CHEMBL2581 P07339 Cathepsin D 94.36% 98.95%
CHEMBL261 P00915 Carbonic anhydrase I 91.24% 96.76%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 90.64% 91.79%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.71% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.56% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 89.28% 90.20%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.35% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.84% 95.89%
CHEMBL2535 P11166 Glucose transporter 87.31% 98.75%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.27% 89.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.36% 85.14%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 86.26% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.20% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.19% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.97% 99.15%
CHEMBL2413 P32246 C-C chemokine receptor type 1 84.13% 89.50%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 83.54% 89.05%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.58% 95.78%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.37% 93.40%

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.
Dracaena cinnabari

Cross-Links

Top
PubChem 162968011
LOTUS LTS0019993
wikiData Q105286969