2,5-Dichloro-3,6-dimethoxybenzoquinone

Details

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Internal ID 925943df-aa5f-44d8-812e-7383ab7cdab0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Benzoquinones > P-benzoquinones
IUPAC Name 2,5-dichloro-3,6-dimethoxycyclohexa-2,5-diene-1,4-dione
SMILES (Canonical) COC1=C(C(=O)C(=C(C1=O)Cl)OC)Cl
SMILES (Isomeric) COC1=C(C(=O)C(=C(C1=O)Cl)OC)Cl
InChI InChI=1S/C8H6Cl2O4/c1-13-7-3(9)6(12)8(14-2)4(10)5(7)11/h1-2H3
InChI Key JQVAMWPWHPTLNU-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6Cl2O4
Molecular Weight 237.03 g/mol
Exact Mass 235.9643141 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2,5-Dichloro-3,6-dimethoxybenzoquinone
3,6-Dichloro-2,5-dimethoxybenzoquinone
84DXP5E8VX
2,5-Dichloro-3,6-dimethoxy-p-benzoquinone
3,6-Dichloro-2,5-dimethoxy-4-benzoquinone
2,5-Cyclohexadiene-1,4-dione, 2,5-dichloro-3,6-dimethoxy-
p-Benzoquinone, 2,5-dichloro-3,6-dimethoxy-
NSC 110655
NSC-110655
3,6-Dichloro-2,5-dimethoxy-p-benzoquinone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,5-Dichloro-3,6-dimethoxybenzoquinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.6621 66.21%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.8185 81.85%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.9635 96.35%
OATP1B3 inhibitior + 0.9717 97.17%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8695 86.95%
P-glycoprotein inhibitior - 0.8852 88.52%
P-glycoprotein substrate - 0.9944 99.44%
CYP3A4 substrate - 0.6163 61.63%
CYP2C9 substrate - 0.8063 80.63%
CYP2D6 substrate - 0.8152 81.52%
CYP3A4 inhibition - 0.7935 79.35%
CYP2C9 inhibition - 0.8903 89.03%
CYP2C19 inhibition + 0.6747 67.47%
CYP2D6 inhibition - 0.8378 83.78%
CYP1A2 inhibition - 0.6422 64.22%
CYP2C8 inhibition - 0.9868 98.68%
CYP inhibitory promiscuity - 0.7188 71.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6551 65.51%
Carcinogenicity (trinary) Non-required 0.4928 49.28%
Eye corrosion - 0.8111 81.11%
Eye irritation + 0.9347 93.47%
Skin irritation - 0.5639 56.39%
Skin corrosion - 0.8218 82.18%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6885 68.85%
Micronuclear + 0.5933 59.33%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation - 0.5300 53.00%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.8658 86.58%
Acute Oral Toxicity (c) III 0.5841 58.41%
Estrogen receptor binding + 0.6064 60.64%
Androgen receptor binding - 0.6981 69.81%
Thyroid receptor binding - 0.6181 61.81%
Glucocorticoid receptor binding - 0.7203 72.03%
Aromatase binding - 0.7193 71.93%
PPAR gamma - 0.6586 65.86%
Honey bee toxicity - 0.8012 80.12%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7700 77.00%
Fish aquatic toxicity + 0.9562 95.62%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.81% 95.56%
CHEMBL2581 P07339 Cathepsin D 85.24% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 80.87% 94.73%

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.
Ailanthus altissima
Eleutherococcus senticosus
Fraxinus chinensis subsp. chinensis
Gynura japonica
Heptapleurum venulosum
Rauvolfia vomitoria
Triticum aestivum

Cross-Links

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PubChem 81630
NPASS NPC138582