3,7-Dihydroxytropolone

Details

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Internal ID 01cae83b-45a1-4e85-932c-23076dd8a6a4
Taxonomy Hydrocarbon derivatives > Tropones > Tropolones
IUPAC Name 2,3,4-trihydroxycyclohepta-2,4,6-trien-1-one
SMILES (Canonical) C1=CC(=O)C(=C(C(=C1)O)O)O
SMILES (Isomeric) C1=CC(=O)C(=C(C(=C1)O)O)O
InChI InChI=1S/C7H6O4/c8-4-2-1-3-5(9)7(11)6(4)10/h1-3H,(H3,8,9,10,11)
InChI Key HQLHJCFATKAUSO-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C7H6O4
Molecular Weight 154.12 g/mol
Exact Mass 154.02660867 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.16
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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85233-29-0
Bmy-28438
2,3,4-trihydroxycyclohepta-2,4,6-trien-1-one
2,3,7-trihydroxycyclohepta-2,4,6-trien-1-one
T7F4GCF4F9
CHEMBL135189
SP15
2,4,6-Cycloheptatrien-1-one, 2,3,4-trihydroxy-
Bmy 28438
2,4,6-Cycloheptatrien-1-one, 2,3,7-trihydroxy-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,7-Dihydroxytropolone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9123 91.23%
Caco-2 + 0.6605 66.05%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.6132 61.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9596 95.96%
OATP1B3 inhibitior + 0.9745 97.45%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9718 97.18%
P-glycoprotein inhibitior - 0.9812 98.12%
P-glycoprotein substrate - 0.9888 98.88%
CYP3A4 substrate - 0.7293 72.93%
CYP2C9 substrate - 0.8264 82.64%
CYP2D6 substrate - 0.8366 83.66%
CYP3A4 inhibition - 0.6472 64.72%
CYP2C9 inhibition - 0.8820 88.20%
CYP2C19 inhibition - 0.9157 91.57%
CYP2D6 inhibition - 0.9286 92.86%
CYP1A2 inhibition - 0.6590 65.90%
CYP2C8 inhibition - 0.9627 96.27%
CYP inhibitory promiscuity - 0.8841 88.41%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7823 78.23%
Carcinogenicity (trinary) Non-required 0.6779 67.79%
Eye corrosion - 0.7700 77.00%
Eye irritation + 0.9939 99.39%
Skin irritation + 0.7864 78.64%
Skin corrosion + 0.8126 81.26%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8733 87.33%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.8451 84.51%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.4551 45.51%
Acute Oral Toxicity (c) III 0.7408 74.08%
Estrogen receptor binding - 0.7655 76.55%
Androgen receptor binding - 0.6666 66.66%
Thyroid receptor binding - 0.6374 63.74%
Glucocorticoid receptor binding - 0.7000 70.00%
Aromatase binding - 0.8267 82.67%
PPAR gamma - 0.5683 56.83%
Honey bee toxicity - 0.9841 98.41%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.8054 80.54%

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 94.76% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 93.50% 91.49%
CHEMBL2581 P07339 Cathepsin D 92.63% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.59% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.18% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 81.63% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 81.53% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.42% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.20% 93.99%

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 128646
LOTUS LTS0188221
wikiData Q83001190