2-[2-(3,7-Dimethylocta-2,6-dienyl)-3,4-dihydroxyphenyl]-5,7-dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-2,3-dihydrochromen-4-one

Details

Top
Internal ID 97488227-9eaf-45d4-82be-1732c0cb1fe8
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 2-prenylated flavans > 2-prenylated flavanones
IUPAC Name 2-[2-(3,7-dimethylocta-2,6-dienyl)-3,4-dihydroxyphenyl]-5,7-dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical) CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC(C(=C)C)O)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCC1=C(C=CC(=C1O)O)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC(C(=C)C)O)O)C)C
InChI InChI=1S/C30H36O7/c1-16(2)7-6-8-18(5)9-10-20-19(11-12-22(31)29(20)35)26-15-25(34)28-27(37-26)14-24(33)21(30(28)36)13-23(32)17(3)4/h7,9,11-12,14,23,26,31-33,35-36H,3,6,8,10,13,15H2,1-2,4-5H3
InChI Key YMILJRPIVTZKTL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H36O7
Molecular Weight 508.60 g/mol
Exact Mass 508.24610348 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP 6.70
Atomic LogP (AlogP) 5.93
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 9

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-[2-(3,7-Dimethylocta-2,6-dienyl)-3,4-dihydroxyphenyl]-5,7-dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-2,3-dihydrochromen-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9556 95.56%
Caco-2 - 0.8183 81.83%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6847 68.47%
OATP2B1 inhibitior - 0.5738 57.38%
OATP1B1 inhibitior + 0.8647 86.47%
OATP1B3 inhibitior + 0.9256 92.56%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9141 91.41%
P-glycoprotein inhibitior + 0.6728 67.28%
P-glycoprotein substrate - 0.5540 55.40%
CYP3A4 substrate + 0.6348 63.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7928 79.28%
CYP3A4 inhibition - 0.5097 50.97%
CYP2C9 inhibition - 0.6803 68.03%
CYP2C19 inhibition - 0.5092 50.92%
CYP2D6 inhibition - 0.8416 84.16%
CYP1A2 inhibition + 0.5617 56.17%
CYP2C8 inhibition + 0.5701 57.01%
CYP inhibitory promiscuity - 0.7504 75.04%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7522 75.22%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.8651 86.51%
Skin irritation - 0.7114 71.14%
Skin corrosion - 0.9242 92.42%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7967 79.67%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.7873 78.73%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.7459 74.59%
Acute Oral Toxicity (c) III 0.3717 37.17%
Estrogen receptor binding + 0.8748 87.48%
Androgen receptor binding + 0.6750 67.50%
Thyroid receptor binding + 0.6356 63.56%
Glucocorticoid receptor binding + 0.7597 75.97%
Aromatase binding + 0.6033 60.33%
PPAR gamma + 0.7546 75.46%
Honey bee toxicity - 0.7495 74.95%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 1.0000 100.00%

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 99.62% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.38% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.96% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.12% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 94.11% 94.73%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 90.86% 92.68%
CHEMBL1951 P21397 Monoamine oxidase A 90.15% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.13% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.11% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.05% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.90% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.21% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.76% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.56% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.36% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.16% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.47% 97.09%
CHEMBL1929 P47989 Xanthine dehydrogenase 84.24% 96.12%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.22% 100.00%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 83.90% 83.10%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 82.02% 98.11%

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.
Macaranga tanarius

Cross-Links

Top
PubChem 72831452
LOTUS LTS0215905
wikiData Q105350552