4,6-Dihydroxy-3,9-dehydromellein

Details

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Internal ID 7d01d995-882d-4519-8fd3-33876b70bf21
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives
IUPAC Name 4,6,8-trihydroxy-3-methylidene-4H-isochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H8O5/c1-4-9(13)6-2-5(11)3-7(12)8(6)10(14)15-4/h2-3,9,11-13H,1H2
InChI Key CDIRPHSIKVTLRY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8O5
Molecular Weight 208.17 g/mol
Exact Mass 208.03717335 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.82
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,6-Dihydroxy-3,9-dehydromellein

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9503 95.03%
Caco-2 - 0.8162 81.62%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4558 45.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8710 87.10%
OATP1B3 inhibitior + 0.8614 86.14%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9865 98.65%
P-glycoprotein inhibitior - 0.9511 95.11%
P-glycoprotein substrate - 0.9806 98.06%
CYP3A4 substrate - 0.5485 54.85%
CYP2C9 substrate - 0.7838 78.38%
CYP2D6 substrate - 0.8395 83.95%
CYP3A4 inhibition + 0.5834 58.34%
CYP2C9 inhibition - 0.5578 55.78%
CYP2C19 inhibition - 0.6220 62.20%
CYP2D6 inhibition - 0.9344 93.44%
CYP1A2 inhibition - 0.6414 64.14%
CYP2C8 inhibition - 0.6935 69.35%
CYP inhibitory promiscuity + 0.6373 63.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9918 99.18%
Carcinogenicity (trinary) Non-required 0.6453 64.53%
Eye corrosion - 0.9719 97.19%
Eye irritation + 0.8826 88.26%
Skin irritation + 0.6170 61.70%
Skin corrosion - 0.9422 94.22%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8739 87.39%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.5427 54.27%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5755 57.55%
Acute Oral Toxicity (c) II 0.4365 43.65%
Estrogen receptor binding + 0.6055 60.55%
Androgen receptor binding + 0.6077 60.77%
Thyroid receptor binding + 0.5163 51.63%
Glucocorticoid receptor binding - 0.5174 51.74%
Aromatase binding + 0.5607 56.07%
PPAR gamma + 0.6400 64.00%
Honey bee toxicity - 0.8675 86.75%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9757 97.57%

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 99.09% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.34% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.93% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.08% 89.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.85% 93.40%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.53% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.49% 99.15%
CHEMBL4530 P00488 Coagulation factor XIII 85.06% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 84.32% 94.73%
CHEMBL1929 P47989 Xanthine dehydrogenase 83.35% 96.12%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.14% 93.99%

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 101805479
LOTUS LTS0041681
wikiData Q75068811