4,5-Dimethoxyphthalic acid

Details

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Internal ID 0a347a24-9799-4d75-af77-d8335ccea039
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > P-methoxybenzoic acids and derivatives
IUPAC Name 4,5-dimethoxyphthalic acid
SMILES (Canonical) COC1=C(C=C(C(=C1)C(=O)O)C(=O)O)OC
SMILES (Isomeric) COC1=C(C=C(C(=C1)C(=O)O)C(=O)O)OC
InChI InChI=1S/C10H10O6/c1-15-7-3-5(9(11)12)6(10(13)14)4-8(7)16-2/h3-4H,1-2H3,(H,11,12)(H,13,14)
InChI Key SKBDLRWFSRLIPP-UHFFFAOYSA-N
Popularity 30 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O6
Molecular Weight 226.18 g/mol
Exact Mass 226.04773803 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.10
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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577-68-4
m-Hemipic acid
m-Hemipinic acid
4,5-dimethoxybenzene-1,2-dicarboxylic acid
4,5-Dimethoxy-1,2-benzenedicarboxylic acid
4,5-Dimethoxy-phthalic acid
Metahemipic acid
metahemipinic acid
1, 4,5-dimethoxy-
4,5-Dimethoxyphthalicacid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4,5-Dimethoxyphthalic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9510 95.10%
Caco-2 + 0.5796 57.96%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.8994 89.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9461 94.61%
OATP1B3 inhibitior + 0.9278 92.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9677 96.77%
P-glycoprotein inhibitior - 0.9121 91.21%
P-glycoprotein substrate - 0.9830 98.30%
CYP3A4 substrate - 0.8301 83.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8571 85.71%
CYP3A4 inhibition - 0.9741 97.41%
CYP2C9 inhibition - 0.8416 84.16%
CYP2C19 inhibition - 0.8758 87.58%
CYP2D6 inhibition - 0.9086 90.86%
CYP1A2 inhibition - 0.8927 89.27%
CYP2C8 inhibition - 0.9307 93.07%
CYP inhibitory promiscuity - 0.9457 94.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6901 69.01%
Carcinogenicity (trinary) Non-required 0.6944 69.44%
Eye corrosion - 0.6056 60.56%
Eye irritation + 0.9866 98.66%
Skin irritation + 0.5726 57.26%
Skin corrosion - 0.8694 86.94%
Ames mutagenesis - 0.7737 77.37%
Human Ether-a-go-go-Related Gene inhibition - 0.8919 89.19%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8712 87.12%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5119 51.19%
Acute Oral Toxicity (c) III 0.5300 53.00%
Estrogen receptor binding + 0.6419 64.19%
Androgen receptor binding - 0.8141 81.41%
Thyroid receptor binding - 0.7474 74.74%
Glucocorticoid receptor binding - 0.6234 62.34%
Aromatase binding - 0.5320 53.20%
PPAR gamma - 0.6808 68.08%
Honey bee toxicity - 0.9608 96.08%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity + 0.9428 94.28%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.44% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.11% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.30% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.31% 95.56%
CHEMBL2535 P11166 Glucose transporter 85.75% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.35% 99.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.29% 93.00%
CHEMBL1255126 O15151 Protein Mdm4 82.72% 90.20%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.77% 94.42%
CHEMBL4208 P20618 Proteasome component C5 81.17% 90.00%
CHEMBL2581 P07339 Cathepsin D 80.80% 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.
Aloe microstigma
Chrozophora plicata
Papaver somniferum

Cross-Links

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PubChem 290988
NPASS NPC176045
LOTUS LTS0031091
wikiData Q82048030