Dehydrocollatolic acid

Details

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Internal ID 18286ba8-b375-4ddf-8c45-3d74a34680c5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Diarylethers
IUPAC Name 5-hydroxy-11-methoxy-6'-methyl-9-(2-oxoheptyl)spiro[1H-isochromeno[5,6-b][1,4]benzodioxepine-2,2'-oxane]-4,8-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H32O9/c1-4-5-6-9-18(30)11-17-12-19(34-3)13-22-24(17)27(32)36-23-14-21(31)25-20(26(23)35-22)15-29(38-28(25)33)10-7-8-16(2)37-29/h12-14,16,31H,4-11,15H2,1-3H3
InChI Key GSGHMIHDUZPOKX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C29H32O9
Molecular Weight 524.60 g/mol
Exact Mass 524.20463259 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.42
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dehydrocollatolic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8717 87.17%
Caco-2 - 0.6838 68.38%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7276 72.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7869 78.69%
OATP1B3 inhibitior - 0.2756 27.56%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9798 97.98%
P-glycoprotein inhibitior + 0.8127 81.27%
P-glycoprotein substrate + 0.5240 52.40%
CYP3A4 substrate + 0.6928 69.28%
CYP2C9 substrate + 0.8060 80.60%
CYP2D6 substrate - 0.8417 84.17%
CYP3A4 inhibition - 0.9184 91.84%
CYP2C9 inhibition - 0.9011 90.11%
CYP2C19 inhibition - 0.7214 72.14%
CYP2D6 inhibition - 0.9376 93.76%
CYP1A2 inhibition - 0.6789 67.89%
CYP2C8 inhibition + 0.7712 77.12%
CYP inhibitory promiscuity - 0.9155 91.55%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7272 72.72%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.8361 83.61%
Skin irritation - 0.7929 79.29%
Skin corrosion - 0.9394 93.94%
Ames mutagenesis - 0.8137 81.37%
Human Ether-a-go-go-Related Gene inhibition - 0.3856 38.56%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation - 0.9142 91.42%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.5773 57.73%
Acute Oral Toxicity (c) III 0.4162 41.62%
Estrogen receptor binding + 0.7730 77.30%
Androgen receptor binding + 0.7533 75.33%
Thyroid receptor binding - 0.5509 55.09%
Glucocorticoid receptor binding + 0.8688 86.88%
Aromatase binding + 0.7243 72.43%
PPAR gamma + 0.6402 64.02%
Honey bee toxicity - 0.8250 82.50%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5781 57.81%
Fish aquatic toxicity + 0.9886 98.86%

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 99.89% 91.11%
CHEMBL240 Q12809 HERG 98.60% 89.76%
CHEMBL2581 P07339 Cathepsin D 98.38% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.48% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.29% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 94.94% 95.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.53% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.35% 93.99%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 94.22% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.65% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.32% 94.80%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.34% 99.23%
CHEMBL4208 P20618 Proteasome component C5 90.11% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.47% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.17% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.85% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.80% 89.00%
CHEMBL5255 O00206 Toll-like receptor 4 86.38% 92.50%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.03% 91.81%
CHEMBL340 P08684 Cytochrome P450 3A4 81.59% 91.19%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.49% 96.77%
CHEMBL3820 P35557 Hexokinase type IV 81.44% 91.96%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.36% 91.07%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.24% 97.25%
CHEMBL1907 P15144 Aminopeptidase N 80.37% 93.31%

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 101104076
LOTUS LTS0031633
wikiData Q77419789