(3S,7R)-7-methoxyresorcylide

Details

Top
Internal ID 654e7ccb-07ac-4a3f-978f-3949ae5db874
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (4S,8R)-14,16-dihydroxy-8-methoxy-4-methyl-3-oxabicyclo[10.4.0]hexadeca-1(12),13,15-triene-2,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O6/c1-10-4-3-5-14(22-2)8-12(18)6-11-7-13(19)9-15(20)16(11)17(21)23-10/h7,9-10,14,19-20H,3-6,8H2,1-2H3/t10-,14+/m0/s1
InChI Key FALVZFIZJLIGBM-IINYFYTJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H22O6
Molecular Weight 322.40 g/mol
Exact Mass 322.14163842 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.34
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3S,7R)-7-methoxyresorcylide

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9126 91.26%
Caco-2 + 0.8121 81.21%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7407 74.07%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8697 86.97%
OATP1B3 inhibitior + 0.9263 92.63%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8300 83.00%
P-glycoprotein inhibitior - 0.7563 75.63%
P-glycoprotein substrate - 0.8458 84.58%
CYP3A4 substrate + 0.5825 58.25%
CYP2C9 substrate + 0.8190 81.90%
CYP2D6 substrate - 0.8599 85.99%
CYP3A4 inhibition + 0.6423 64.23%
CYP2C9 inhibition - 0.8444 84.44%
CYP2C19 inhibition - 0.7758 77.58%
CYP2D6 inhibition - 0.8695 86.95%
CYP1A2 inhibition + 0.7246 72.46%
CYP2C8 inhibition - 0.6174 61.74%
CYP inhibitory promiscuity - 0.9145 91.45%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8711 87.11%
Carcinogenicity (trinary) Non-required 0.7759 77.59%
Eye corrosion - 0.9760 97.60%
Eye irritation - 0.7259 72.59%
Skin irritation - 0.7597 75.97%
Skin corrosion - 0.9314 93.14%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3992 39.92%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6532 65.32%
skin sensitisation - 0.8695 86.95%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7974 79.74%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.6264 62.64%
Acute Oral Toxicity (c) III 0.4018 40.18%
Estrogen receptor binding + 0.7089 70.89%
Androgen receptor binding + 0.7589 75.89%
Thyroid receptor binding - 0.6825 68.25%
Glucocorticoid receptor binding + 0.6861 68.61%
Aromatase binding - 0.5156 51.56%
PPAR gamma + 0.7689 76.89%
Honey bee toxicity - 0.8858 88.58%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9694 96.94%

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 98.56% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.14% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.75% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.00% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.13% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.25% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.67% 94.45%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.15% 96.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.66% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.46% 96.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.95% 99.18%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.50% 99.23%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 85.30% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.67% 86.33%
CHEMBL1902 P62942 FK506-binding protein 1A 83.36% 97.05%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.92% 91.07%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.48% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.32% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.57% 99.17%
CHEMBL5255 O00206 Toll-like receptor 4 80.89% 92.50%
CHEMBL217 P14416 Dopamine D2 receptor 80.85% 95.62%

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 102329741
LOTUS LTS0140186
wikiData Q104992315