3,5-dimethoxydihydrofusarubin D

Details

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Internal ID e0adcdea-127f-4f88-8934-40d48f278e29
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name (3R,4aS,5S,10aR)-6,9-dihydroxy-3,5,7-trimethoxy-3-methyl-4,4a,5,10a-tetrahydro-1H-benzo[g]isochromen-10-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O7/c1-17(23-4)6-8-9(7-24-17)14(19)12-10(18)5-11(21-2)15(20)13(12)16(8)22-3/h5,8-9,16,18,20H,6-7H2,1-4H3/t8-,9-,16-,17+/m0/s1
InChI Key WIJFPHJXBDLXRE-KRQUVALZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O7
Molecular Weight 338.40 g/mol
Exact Mass 338.13655304 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.01
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,5-dimethoxydihydrofusarubin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9261 92.61%
Caco-2 + 0.7897 78.97%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7309 73.09%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.8678 86.78%
OATP1B3 inhibitior + 0.9002 90.02%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5969 59.69%
P-glycoprotein inhibitior - 0.6938 69.38%
P-glycoprotein substrate - 0.6378 63.78%
CYP3A4 substrate + 0.6553 65.53%
CYP2C9 substrate - 0.8028 80.28%
CYP2D6 substrate - 0.8318 83.18%
CYP3A4 inhibition - 0.7845 78.45%
CYP2C9 inhibition - 0.9103 91.03%
CYP2C19 inhibition - 0.8215 82.15%
CYP2D6 inhibition - 0.9032 90.32%
CYP1A2 inhibition + 0.7104 71.04%
CYP2C8 inhibition - 0.5832 58.32%
CYP inhibitory promiscuity - 0.8654 86.54%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6694 66.94%
Eye corrosion - 0.9870 98.70%
Eye irritation - 0.7920 79.20%
Skin irritation - 0.7931 79.31%
Skin corrosion - 0.9684 96.84%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7642 76.42%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5025 50.25%
skin sensitisation - 0.8618 86.18%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6064 60.64%
Acute Oral Toxicity (c) III 0.6546 65.46%
Estrogen receptor binding + 0.8356 83.56%
Androgen receptor binding + 0.7436 74.36%
Thyroid receptor binding + 0.6800 68.00%
Glucocorticoid receptor binding + 0.8834 88.34%
Aromatase binding - 0.6250 62.50%
PPAR gamma + 0.6606 66.06%
Honey bee toxicity - 0.7922 79.22%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9574 95.74%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.74% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.18% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.93% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 95.39% 92.94%
CHEMBL4040 P28482 MAP kinase ERK2 93.11% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.41% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.16% 86.33%
CHEMBL2581 P07339 Cathepsin D 90.45% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.63% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.48% 89.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.48% 96.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.83% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.87% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 83.84% 94.75%
CHEMBL340 P08684 Cytochrome P450 3A4 83.65% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.12% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.82% 92.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.26% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.21% 97.14%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.15% 91.07%
CHEMBL4208 P20618 Proteasome component C5 80.25% 90.00%

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.
There are no matching plants.

Cross-Links

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PubChem 101537879
LOTUS LTS0021114
wikiData Q77493286