Hesseltin B

Details

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Internal ID 4837e7dc-08a1-4165-8d5b-baf415086965
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (1R,2R,7S,10R)-7-hydroxy-2,6,6,10-tetramethyl-14-[(1E,3E)-penta-1,3-dienyl]-11,13-dioxatetracyclo[8.8.0.02,7.012,17]octadeca-12(17),14-diene-5,16-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H32O5/c1-6-7-8-9-16-14-18(26)17-15-19-23(4)11-10-20(27)22(2,3)25(23,28)13-12-24(19,5)30-21(17)29-16/h6-9,14,19,28H,10-13,15H2,1-5H3/b7-6+,9-8+/t19-,23-,24-,25-/m1/s1
InChI Key XXHQUPUACYOBLJ-LRJFGXOXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H32O5
Molecular Weight 412.50 g/mol
Exact Mass 412.22497412 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.46
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hesseltin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9841 98.41%
Caco-2 + 0.5060 50.60%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8302 83.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8627 86.27%
OATP1B3 inhibitior - 0.2712 27.12%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8071 80.71%
BSEP inhibitior + 0.9578 95.78%
P-glycoprotein inhibitior + 0.5932 59.32%
P-glycoprotein substrate - 0.5888 58.88%
CYP3A4 substrate + 0.6614 66.14%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8488 84.88%
CYP3A4 inhibition - 0.6600 66.00%
CYP2C9 inhibition - 0.8757 87.57%
CYP2C19 inhibition - 0.8606 86.06%
CYP2D6 inhibition - 0.9555 95.55%
CYP1A2 inhibition - 0.6391 63.91%
CYP2C8 inhibition + 0.5142 51.42%
CYP inhibitory promiscuity - 0.9769 97.69%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6325 63.25%
Eye corrosion - 0.9929 99.29%
Eye irritation - 0.9266 92.66%
Skin irritation - 0.6212 62.12%
Skin corrosion - 0.9169 91.69%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8701 87.01%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.5981 59.81%
skin sensitisation - 0.8281 82.81%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.6498 64.98%
Acute Oral Toxicity (c) III 0.4071 40.71%
Estrogen receptor binding + 0.8190 81.90%
Androgen receptor binding + 0.7419 74.19%
Thyroid receptor binding + 0.6668 66.68%
Glucocorticoid receptor binding + 0.7881 78.81%
Aromatase binding + 0.7525 75.25%
PPAR gamma + 0.7268 72.68%
Honey bee toxicity - 0.8092 80.92%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9957 99.57%

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 97.99% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.36% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.35% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.91% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 92.85% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.54% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 91.19% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.77% 93.99%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.86% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.70% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.61% 92.94%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.53% 82.69%
CHEMBL217 P14416 Dopamine D2 receptor 83.07% 95.62%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 82.95% 85.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.52% 85.14%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.03% 85.30%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.47% 99.23%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.13% 93.40%

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 51039160
LOTUS LTS0264606
wikiData Q77386153