Dalenin

Details

Top
Internal ID fcadfb2e-5106-4a35-a837-197f872b5573
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Pyranoflavonoids
IUPAC Name 8-(2,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one
SMILES (Canonical) CC1(C=CC2=C(C3=C(C=C2O1)OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C
SMILES (Isomeric) CC1(C=CC2=C(C3=C(C=C2O1)OC(CC3=O)C4=C(C=C(C=C4)O)O)O)C
InChI InChI=1S/C20H18O6/c1-20(2)6-5-12-16(26-20)9-17-18(19(12)24)14(23)8-15(25-17)11-4-3-10(21)7-13(11)22/h3-7,9,15,21-22,24H,8H2,1-2H3
InChI Key OBECBPJJXYKUJE-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C20H18O6
Molecular Weight 354.40 g/mol
Exact Mass 354.11033829 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.69
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

Top
CHEMBL2147165
BDBM50485661

2D Structure

Top
2D Structure of Dalenin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9643 96.43%
Caco-2 + 0.5718 57.18%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8225 82.25%
OATP2B1 inhibitior - 0.5851 58.51%
OATP1B1 inhibitior + 0.8878 88.78%
OATP1B3 inhibitior + 0.9730 97.30%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7224 72.24%
P-glycoprotein inhibitior - 0.7127 71.27%
P-glycoprotein substrate + 0.5528 55.28%
CYP3A4 substrate + 0.6490 64.90%
CYP2C9 substrate - 0.7981 79.81%
CYP2D6 substrate - 0.8063 80.63%
CYP3A4 inhibition + 0.7916 79.16%
CYP2C9 inhibition + 0.8250 82.50%
CYP2C19 inhibition + 0.7419 74.19%
CYP2D6 inhibition - 0.7617 76.17%
CYP1A2 inhibition + 0.5879 58.79%
CYP2C8 inhibition + 0.4819 48.19%
CYP inhibitory promiscuity + 0.7415 74.15%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5064 50.64%
Eye corrosion - 0.9918 99.18%
Eye irritation + 0.6499 64.99%
Skin irritation - 0.7230 72.30%
Skin corrosion - 0.9050 90.50%
Ames mutagenesis + 0.5163 51.63%
Human Ether-a-go-go-Related Gene inhibition - 0.7239 72.39%
Micronuclear + 0.6959 69.59%
Hepatotoxicity - 0.5074 50.74%
skin sensitisation - 0.7943 79.43%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.5958 59.58%
Acute Oral Toxicity (c) III 0.5088 50.88%
Estrogen receptor binding + 0.8593 85.93%
Androgen receptor binding + 0.7144 71.44%
Thyroid receptor binding + 0.7029 70.29%
Glucocorticoid receptor binding + 0.8196 81.96%
Aromatase binding + 0.5307 53.07%
PPAR gamma + 0.8549 85.49%
Honey bee toxicity - 0.8497 84.97%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9578 95.78%

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 98.89% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.38% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.43% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.12% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.04% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.68% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.35% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.27% 90.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.62% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.02% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.69% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.45% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.01% 93.99%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.90% 93.40%
CHEMBL4208 P20618 Proteasome component C5 86.39% 90.00%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 85.80% 85.11%
CHEMBL1929 P47989 Xanthine dehydrogenase 83.21% 96.12%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.52% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.36% 100.00%
CHEMBL236 P41143 Delta opioid receptor 81.46% 99.35%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.05% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.01% 97.09%

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.
Dalea elegans

Cross-Links

Top
PubChem 53249095
NPASS NPC470647
ChEMBL CHEMBL2147165