Dehydroisosulochrin

Details

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Internal ID 2e64f8df-aa90-42f1-9d29-cabbe109150a
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl 8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14O6/c1-8-4-11(18)15-12(5-8)23-13-7-9(21-2)6-10(17(20)22-3)14(13)16(15)19/h4-7,18H,1-3H3
InChI Key FLSZNPRKDAAYOZ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O6
Molecular Weight 314.29 g/mol
Exact Mass 314.07903816 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.76
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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Isosulochrin dehydrate
0Z737D25TT
UNII-0Z737D25TT
Methyl 8-hydroxy-3-methoxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate
9H-Xanthene-1-carboxylic acid, 8-hydroxy-3-methoxy-6-methyl-9-oxo-, methyl ester
77282-74-7
Q27251072

2D Structure

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2D Structure of Dehydroisosulochrin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9626 96.26%
Caco-2 + 0.9025 90.25%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6628 66.28%
OATP2B1 inhibitior - 0.7194 71.94%
OATP1B1 inhibitior + 0.8693 86.93%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5989 59.89%
P-glycoprotein inhibitior - 0.4739 47.39%
P-glycoprotein substrate - 0.8917 89.17%
CYP3A4 substrate + 0.5245 52.45%
CYP2C9 substrate - 0.5872 58.72%
CYP2D6 substrate - 0.8705 87.05%
CYP3A4 inhibition - 0.8128 81.28%
CYP2C9 inhibition - 0.9481 94.81%
CYP2C19 inhibition - 0.9692 96.92%
CYP2D6 inhibition - 0.9333 93.33%
CYP1A2 inhibition + 0.5934 59.34%
CYP2C8 inhibition - 0.6481 64.81%
CYP inhibitory promiscuity - 0.8784 87.84%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.5330 53.30%
Eye corrosion - 0.9560 95.60%
Eye irritation + 0.8133 81.33%
Skin irritation - 0.7766 77.66%
Skin corrosion - 0.9855 98.55%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5904 59.04%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.6476 64.76%
skin sensitisation - 0.9709 97.09%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.5689 56.89%
Acute Oral Toxicity (c) II 0.5201 52.01%
Estrogen receptor binding + 0.8071 80.71%
Androgen receptor binding + 0.7497 74.97%
Thyroid receptor binding - 0.5101 51.01%
Glucocorticoid receptor binding + 0.8115 81.15%
Aromatase binding + 0.7124 71.24%
PPAR gamma + 0.7985 79.85%
Honey bee toxicity - 0.9072 90.72%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9018 90.18%

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 97.65% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.53% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.50% 94.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 91.57% 81.11%
CHEMBL3401 O75469 Pregnane X receptor 90.45% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.59% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.78% 99.23%
CHEMBL2581 P07339 Cathepsin D 87.64% 98.95%
CHEMBL4208 P20618 Proteasome component C5 87.06% 90.00%
CHEMBL2535 P11166 Glucose transporter 86.80% 98.75%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 86.72% 87.67%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.38% 94.42%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.89% 99.15%
CHEMBL340 P08684 Cytochrome P450 3A4 85.79% 91.19%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.10% 93.65%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.26% 99.17%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.19% 94.80%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.18% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.54% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.41% 89.00%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 80.19% 80.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Rhizophora apiculata

Cross-Links

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PubChem 101122392
LOTUS LTS0201861
wikiData Q27251072