Streptopyrone

Details

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Internal ID 1af97704-bbf7-43a7-8c53-ffc3fa892980
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name (3S)-3-hydroxy-5-methoxy-6-methyl-2,3-dihydropyran-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H10O4/c1-4-7(10-2)6(9)5(8)3-11-4/h5,8H,3H2,1-2H3/t5-/m0/s1
InChI Key JOWYHBUWSWRYOG-YFKPBYRVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C7H10O4
Molecular Weight 158.15 g/mol
Exact Mass 158.05790880 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.18
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Streptopyrone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9678 96.78%
Caco-2 - 0.6384 63.84%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7767 77.67%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.9703 97.03%
OATP1B3 inhibitior + 0.9710 97.10%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9429 94.29%
P-glycoprotein inhibitior - 0.9761 97.61%
P-glycoprotein substrate - 0.9601 96.01%
CYP3A4 substrate - 0.5807 58.07%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.8675 86.75%
CYP3A4 inhibition - 0.9178 91.78%
CYP2C9 inhibition - 0.9895 98.95%
CYP2C19 inhibition - 0.8956 89.56%
CYP2D6 inhibition - 0.9288 92.88%
CYP1A2 inhibition - 0.8464 84.64%
CYP2C8 inhibition - 0.9873 98.73%
CYP inhibitory promiscuity - 0.9361 93.61%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8728 87.28%
Carcinogenicity (trinary) Non-required 0.7682 76.82%
Eye corrosion - 0.9394 93.94%
Eye irritation + 0.9793 97.93%
Skin irritation - 0.5913 59.13%
Skin corrosion - 0.9572 95.72%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7984 79.84%
Micronuclear - 0.6341 63.41%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8010 80.10%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6466 64.66%
Acute Oral Toxicity (c) III 0.5004 50.04%
Estrogen receptor binding - 0.7958 79.58%
Androgen receptor binding - 0.8025 80.25%
Thyroid receptor binding - 0.7987 79.87%
Glucocorticoid receptor binding - 0.8989 89.89%
Aromatase binding - 0.8710 87.10%
PPAR gamma - 0.8206 82.06%
Honey bee toxicity - 0.9245 92.45%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.7662 76.62%

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 89.74% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.05% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.19% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.69% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.06% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.76% 91.11%

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 101599037
LOTUS LTS0032194
wikiData Q77492275