Hesseltin D

Details

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Internal ID 1022eb09-d3f7-4d82-8468-05cbbac082b0
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (2R,7S,10R)-7-hydroxy-2-(hydroxymethyl)-6,6,10-trimethyl-14-[(1E,3E)-penta-1,3-dienyl]-11,13-dioxatetracyclo[8.8.0.02,7.012,17]octadeca-1(18),12(17),14-triene-5,16-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H30O6/c1-5-6-7-8-16-13-18(27)17-14-19-23(4,31-21(17)30-16)11-12-25(29)22(2,3)20(28)9-10-24(19,25)15-26/h5-8,13-14,26,29H,9-12,15H2,1-4H3/b6-5+,8-7+/t23-,24+,25-/m1/s1
InChI Key XTZQCANTSHHQLQ-ZYAPZJJMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H30O6
Molecular Weight 426.50 g/mol
Exact Mass 426.20423867 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.66
H-Bond Acceptor 6
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 Hesseltin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9646 96.46%
Caco-2 - 0.6072 60.72%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8222 82.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8466 84.66%
OATP1B3 inhibitior - 0.2410 24.10%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6391 63.91%
BSEP inhibitior + 0.9625 96.25%
P-glycoprotein inhibitior + 0.6584 65.84%
P-glycoprotein substrate - 0.5081 50.81%
CYP3A4 substrate + 0.6657 66.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8482 84.82%
CYP3A4 inhibition + 0.5567 55.67%
CYP2C9 inhibition - 0.7891 78.91%
CYP2C19 inhibition - 0.8225 82.25%
CYP2D6 inhibition - 0.9132 91.32%
CYP1A2 inhibition - 0.5619 56.19%
CYP2C8 inhibition - 0.5940 59.40%
CYP inhibitory promiscuity - 0.8757 87.57%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6195 61.95%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.8772 87.72%
Skin irritation - 0.6561 65.61%
Skin corrosion - 0.9445 94.45%
Ames mutagenesis - 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8954 89.54%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.5226 52.26%
skin sensitisation - 0.8628 86.28%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7878 78.78%
Acute Oral Toxicity (c) III 0.6024 60.24%
Estrogen receptor binding + 0.8469 84.69%
Androgen receptor binding + 0.7942 79.42%
Thyroid receptor binding + 0.6831 68.31%
Glucocorticoid receptor binding + 0.7568 75.68%
Aromatase binding + 0.7950 79.50%
PPAR gamma + 0.7448 74.48%
Honey bee toxicity - 0.8551 85.51%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9930 99.30%

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 98.08% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 97.30% 89.63%
CHEMBL3192 Q9BY41 Histone deacetylase 8 96.21% 93.99%
CHEMBL2581 P07339 Cathepsin D 94.49% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.88% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 91.03% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.38% 86.33%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.87% 82.69%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.28% 93.40%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.17% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.21% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.01% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.74% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 82.33% 94.73%
CHEMBL4208 P20618 Proteasome component C5 81.42% 90.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.20% 91.07%

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 52920974
LOTUS LTS0268718
wikiData Q77516490