Dracorhodin

Details

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Internal ID ccfd807c-3d27-4229-92c5-0ee8aa6dae07
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 5-O-methylated flavonoids
IUPAC Name 5-methoxy-6-methyl-2-phenylchromen-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14O3/c1-11-14(18)10-16-13(17(11)19-2)8-9-15(20-16)12-6-4-3-5-7-12/h3-10H,1-2H3
InChI Key UCZJPQIEFFTIEV-UHFFFAOYSA-N
Popularity 32 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O3
Molecular Weight 266.29 g/mol
Exact Mass 266.094294304 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.73
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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643-56-1
5-methoxy-6-methyl-2-phenylchromen-7-one
C4TSX5M53X
5-Methoxy-6-methyl-2-phenyl-7H-1-benzopyran-7-one
DTXSID20214526
NSC-234485
RefChem:135758
DTXCID50137017
5-Methoxy-6-methyl-2-phenyl-7H-chromen-7-one
C.I. 75210
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dracorhodin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.8970 89.70%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7970 79.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9378 93.78%
OATP1B3 inhibitior + 0.9955 99.55%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4909 49.09%
P-glycoprotein inhibitior + 0.8300 83.00%
P-glycoprotein substrate - 0.9000 90.00%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7888 78.88%
CYP3A4 inhibition - 0.6173 61.73%
CYP2C9 inhibition + 0.8949 89.49%
CYP2C19 inhibition + 0.9597 95.97%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition + 0.9840 98.40%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.8372 83.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.5654 56.54%
Eye corrosion - 0.8611 86.11%
Eye irritation - 0.6624 66.24%
Skin irritation - 0.5763 57.63%
Skin corrosion - 0.9738 97.38%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7364 73.64%
Micronuclear + 0.7359 73.59%
Hepatotoxicity + 0.5785 57.85%
skin sensitisation - 0.8969 89.69%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.5817 58.17%
Acute Oral Toxicity (c) III 0.6264 62.64%
Estrogen receptor binding + 0.9441 94.41%
Androgen receptor binding + 0.9043 90.43%
Thyroid receptor binding + 0.5976 59.76%
Glucocorticoid receptor binding + 0.7978 79.78%
Aromatase binding + 0.8995 89.95%
PPAR gamma + 0.6659 66.59%
Honey bee toxicity - 0.8433 84.33%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.8312 83.12%

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
CHEMBL2581 P07339 Cathepsin D 96.59% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.39% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.53% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.56% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 90.83% 93.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.29% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.68% 96.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.08% 93.99%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 84.97% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.14% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.99% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.61% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.66% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.11% 96.67%

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.
Calamus draco

Cross-Links

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PubChem 69509
NPASS NPC5472
LOTUS LTS0073919
wikiData Q83090389