Microthecin

Details

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Internal ID bc7e35e6-010e-4d44-9a5b-b50918b31649
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name 6-hydroxy-6-(hydroxymethyl)-2H-pyran-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H8O4/c7-4-6(9)5(8)2-1-3-10-6/h1-2,7,9H,3-4H2
InChI Key FUJVJJBVXLPRQJ-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8O4
Molecular Weight 144.12 g/mol
Exact Mass 144.04225873 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP -0.80
Atomic LogP (AlogP) -1.18
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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2-hydroxy-2-(hydroxymethyl)-2H-pyran-3(6H)-one
6-hydroxy-6-(hydroxymethyl)-2H-pyran-5-one
CHEBI:51835
RefChem:158806
73033-01-9
SCHEMBL7065396
C19821
Q27122809

2D Structure

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2D Structure of Microthecin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7419 74.19%
Caco-2 + 0.5919 59.19%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8265 82.65%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.9514 95.14%
OATP1B3 inhibitior + 0.9634 96.34%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9391 93.91%
P-glycoprotein inhibitior - 0.9900 99.00%
P-glycoprotein substrate - 0.9663 96.63%
CYP3A4 substrate - 0.6123 61.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8684 86.84%
CYP3A4 inhibition - 0.9610 96.10%
CYP2C9 inhibition - 0.9674 96.74%
CYP2C19 inhibition - 0.9118 91.18%
CYP2D6 inhibition - 0.9476 94.76%
CYP1A2 inhibition - 0.9619 96.19%
CYP2C8 inhibition - 0.9801 98.01%
CYP inhibitory promiscuity - 0.9866 98.66%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6810 68.10%
Eye corrosion - 0.9789 97.89%
Eye irritation + 0.8262 82.62%
Skin irritation - 0.8193 81.93%
Skin corrosion - 0.9145 91.45%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7930 79.30%
Micronuclear - 0.8041 80.41%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.8800 88.00%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.7207 72.07%
Acute Oral Toxicity (c) III 0.4594 45.94%
Estrogen receptor binding - 0.8965 89.65%
Androgen receptor binding - 0.7571 75.71%
Thyroid receptor binding - 0.8050 80.50%
Glucocorticoid receptor binding - 0.8304 83.04%
Aromatase binding - 0.7818 78.18%
PPAR gamma - 0.7834 78.34%
Honey bee toxicity - 0.9455 94.55%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.6565 65.65%

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 96.39% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.05% 94.45%
CHEMBL2581 P07339 Cathepsin D 84.82% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.64% 96.09%
CHEMBL4208 P20618 Proteasome component C5 81.98% 90.00%

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 10130020
LOTUS LTS0114940
wikiData Q27122809