(3R,4aS,5S,10aR)-5-hydroxydihydrofusarubin D

Details

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Internal ID 07d14b15-d287-4f54-8fed-9ca3813f07b3
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name (3R,4aS,5S,10aR)-3,5,6,9-tetrahydroxy-7-methoxy-3-methyl-4,4a,5,10a-tetrahydro-1H-benzo[g]isochromen-10-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H18O7/c1-15(20)4-6-7(5-22-15)13(18)10-8(16)3-9(21-2)14(19)11(10)12(6)17/h3,6-7,12,16-17,19-20H,4-5H2,1-2H3/t6-,7-,12-,15+/m0/s1
InChI Key UHLYLCLJRKLDOP-IKRVUARBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O7
Molecular Weight 310.30 g/mol
Exact Mass 310.10525291 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.70
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,4aS,5S,10aR)-5-hydroxydihydrofusarubin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8615 86.15%
Caco-2 - 0.6151 61.51%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.5610 56.10%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.8639 86.39%
OATP1B3 inhibitior + 0.9214 92.14%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8470 84.70%
P-glycoprotein inhibitior - 0.9198 91.98%
P-glycoprotein substrate - 0.7266 72.66%
CYP3A4 substrate + 0.6324 63.24%
CYP2C9 substrate - 0.8106 81.06%
CYP2D6 substrate - 0.8216 82.16%
CYP3A4 inhibition - 0.5882 58.82%
CYP2C9 inhibition - 0.8943 89.43%
CYP2C19 inhibition - 0.8442 84.42%
CYP2D6 inhibition - 0.7951 79.51%
CYP1A2 inhibition + 0.5382 53.82%
CYP2C8 inhibition - 0.6311 63.11%
CYP inhibitory promiscuity - 0.9039 90.39%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6876 68.76%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.8254 82.54%
Skin irritation - 0.7498 74.98%
Skin corrosion - 0.9450 94.50%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7628 76.28%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.5295 52.95%
skin sensitisation - 0.8777 87.77%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6202 62.02%
Acute Oral Toxicity (c) III 0.6337 63.37%
Estrogen receptor binding + 0.7055 70.55%
Androgen receptor binding + 0.6705 67.05%
Thyroid receptor binding + 0.5480 54.80%
Glucocorticoid receptor binding + 0.9204 92.04%
Aromatase binding - 0.6700 67.00%
PPAR gamma + 0.5836 58.36%
Honey bee toxicity - 0.8000 80.00%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5149 51.49%
Fish aquatic toxicity + 0.9309 93.09%

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 99.68% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.87% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 95.45% 92.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.87% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.88% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.53% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.31% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.22% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.03% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 85.80% 91.19%
CHEMBL2581 P07339 Cathepsin D 85.69% 98.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.30% 97.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.92% 100.00%
CHEMBL4208 P20618 Proteasome component C5 82.58% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.07% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.59% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.46% 96.21%
CHEMBL1937 Q92769 Histone deacetylase 2 81.05% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.05% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.73% 99.23%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101537874
LOTUS LTS0185155
wikiData Q77386251