1,4-Cyclohexadiene-1,2-dicarboxylic anhydride

Details

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Internal ID 24799876-a9f6-47f7-a9b7-71e59252ebbc
Taxonomy Organoheterocyclic compounds > Isobenzofurans
IUPAC Name 4,7-dihydro-2-benzofuran-1,3-dione
SMILES (Canonical) C1C=CCC2=C1C(=O)OC2=O
SMILES (Isomeric) C1C=CCC2=C1C(=O)OC2=O
InChI InChI=1S/C8H6O3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-2H,3-4H2
InChI Key XCGJCRKHWHYKIE-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6O3
Molecular Weight 150.13 g/mol
Exact Mass 150.031694049 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.72
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1,4-Cyclohexadiene-1,2-dicarboxylic anhydride
4,7-Dihydro-2-benzofuran-1,3-dione
1,3-Isobenzofurandione, 4,7-dihydro-
1,4-CYCLOHEXADIENE-1,2-DICARBOXYLICANHYDRIDE
3,6-Dihydrophthalic anhydride
NSC122938
SCHEMBL1045077
DTXSID00197262
isobenzofuran-1,3(4H,7H)-dione
AKOS006274922
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,4-Cyclohexadiene-1,2-dicarboxylic anhydride

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5747 57.47%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.4739 47.39%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9706 97.06%
OATP1B3 inhibitior + 0.9636 96.36%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9400 94.00%
P-glycoprotein inhibitior - 0.9868 98.68%
P-glycoprotein substrate - 0.9960 99.60%
CYP3A4 substrate - 0.7506 75.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8352 83.52%
CYP3A4 inhibition - 0.8841 88.41%
CYP2C9 inhibition - 0.8691 86.91%
CYP2C19 inhibition - 0.8426 84.26%
CYP2D6 inhibition - 0.9296 92.96%
CYP1A2 inhibition - 0.6027 60.27%
CYP2C8 inhibition - 0.9954 99.54%
CYP inhibitory promiscuity - 0.8220 82.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9162 91.62%
Carcinogenicity (trinary) Non-required 0.5758 57.58%
Eye corrosion + 0.9651 96.51%
Eye irritation + 0.9814 98.14%
Skin irritation + 0.6871 68.71%
Skin corrosion - 0.7666 76.66%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7290 72.90%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.7928 79.28%
skin sensitisation - 0.5764 57.64%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity + 1.0000 100.00%
Nephrotoxicity + 0.6563 65.63%
Acute Oral Toxicity (c) III 0.6960 69.60%
Estrogen receptor binding - 0.9646 96.46%
Androgen receptor binding - 0.5665 56.65%
Thyroid receptor binding - 0.8882 88.82%
Glucocorticoid receptor binding - 0.9427 94.27%
Aromatase binding - 0.8335 83.35%
PPAR gamma - 0.8065 80.65%
Honey bee toxicity - 0.9254 92.54%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9752 97.52%

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 91.96% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.61% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.08% 98.95%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis
Conioselinum anthriscoides
Ligusticum officinale

Cross-Links

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PubChem 138348
NPASS NPC129655