Stipitatic acid

Details

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Internal ID 59ed88e3-a36e-4aa4-824f-dd791ed31b79
Taxonomy Hydrocarbon derivatives > Tropones
IUPAC Name 5,6-dihydroxy-3-oxocyclohepta-1,4,6-triene-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H6O5/c9-5-1-4(8(12)13)2-6(10)7(11)3-5/h1-3,10-11H,(H,12,13)
InChI Key ZGKNMKBZOSTFCB-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6O5
Molecular Weight 182.13 g/mol
Exact Mass 182.02152329 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP -0.40
Atomic LogP (AlogP) 0.16
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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4440-39-5
3,6-Dihydroxy-5-oxo-1,3,6-cycloheptatriene-1-carboxylic acid
Stipitatate
35DNB4NP54
1,3,6-CYCLOHEPTATRIENE-1-CARBOXYLIC ACID, 3,6-DIHYDROXY-5-OXO-
3,6-dihydroxy-5-oxocyclohepta-1,3,6-triene-1-carboxylic acid
BRN 2723909
UNII-35DNB4NP54
4-10-00-03859 (Beilstein Handbook Reference)
SCHEMBL21100915
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Stipitatic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8922 89.22%
Caco-2 - 0.5379 53.79%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7734 77.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9641 96.41%
OATP1B3 inhibitior + 0.9620 96.20%
MATE1 inhibitior + 0.6200 62.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9835 98.35%
P-glycoprotein inhibitior - 0.9818 98.18%
P-glycoprotein substrate - 0.9937 99.37%
CYP3A4 substrate - 0.7880 78.80%
CYP2C9 substrate - 0.6673 66.73%
CYP2D6 substrate - 0.8963 89.63%
CYP3A4 inhibition - 0.9447 94.47%
CYP2C9 inhibition - 0.9296 92.96%
CYP2C19 inhibition - 0.9596 95.96%
CYP2D6 inhibition - 0.9395 93.95%
CYP1A2 inhibition - 0.9558 95.58%
CYP2C8 inhibition - 0.9575 95.75%
CYP inhibitory promiscuity - 0.9904 99.04%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7197 71.97%
Carcinogenicity (trinary) Non-required 0.6772 67.72%
Eye corrosion - 0.8329 83.29%
Eye irritation + 0.9971 99.71%
Skin irritation + 0.7416 74.16%
Skin corrosion + 0.7846 78.46%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9086 90.86%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.6283 62.83%
skin sensitisation + 0.5733 57.33%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5664 56.64%
Acute Oral Toxicity (c) III 0.4920 49.20%
Estrogen receptor binding - 0.8319 83.19%
Androgen receptor binding - 0.4825 48.25%
Thyroid receptor binding - 0.8052 80.52%
Glucocorticoid receptor binding - 0.5572 55.72%
Aromatase binding - 0.7996 79.96%
PPAR gamma - 0.6447 64.47%
Honey bee toxicity - 0.9496 94.96%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity + 0.9355 93.55%

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 93.60% 91.11%
CHEMBL3194 P02766 Transthyretin 90.52% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.88% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 87.15% 83.82%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.41% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.44% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.11% 99.17%
CHEMBL1811 P34995 Prostanoid EP1 receptor 81.60% 95.71%
CHEMBL2581 P07339 Cathepsin D 81.58% 98.95%

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 20501
LOTUS LTS0026915
wikiData Q105375286