Isochroman-4-one

Details

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Internal ID 87990557-221c-4c39-8a5c-ac01ac6fa45b
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 1H-isochromen-4-one
SMILES (Canonical) C1C2=CC=CC=C2C(=O)CO1
SMILES (Isomeric) C1C2=CC=CC=C2C(=O)CO1
InChI InChI=1S/C9H8O2/c10-9-6-11-5-7-3-1-2-4-8(7)9/h1-4H,5-6H2
InChI Key OYXTZAZUFUWSIR-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8O2
Molecular Weight 148.16 g/mol
Exact Mass 148.052429494 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.40
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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20924-56-5
4-ISOCHROMANONE
3,4-dihydro-1H-2-benzopyran-4-one
1H-2-Benzopyran-4(3H)-one
1H-isochromen-4-one
1H-isochromen-4(3H)-one
MFCD09744058
1H-2-Benzopyran-4-ol, AldrichCPR
SCHEMBL135207
DTXSID40491796
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isochroman-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.9207 92.07%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.6401 64.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9446 94.46%
OATP1B3 inhibitior + 0.9719 97.19%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8832 88.32%
P-glycoprotein inhibitior - 0.9898 98.98%
P-glycoprotein substrate - 0.9777 97.77%
CYP3A4 substrate - 0.6368 63.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.9602 96.02%
CYP2C9 inhibition - 0.5875 58.75%
CYP2C19 inhibition + 0.7086 70.86%
CYP2D6 inhibition - 0.8819 88.19%
CYP1A2 inhibition + 0.7709 77.09%
CYP2C8 inhibition - 0.9823 98.23%
CYP inhibitory promiscuity - 0.7267 72.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5782 57.82%
Eye corrosion - 0.8825 88.25%
Eye irritation + 0.9969 99.69%
Skin irritation - 0.5921 59.21%
Skin corrosion - 0.9445 94.45%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8004 80.04%
Micronuclear - 0.6599 65.99%
Hepatotoxicity + 0.7569 75.69%
skin sensitisation + 0.5097 50.97%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.7585 75.85%
Acute Oral Toxicity (c) III 0.6426 64.26%
Estrogen receptor binding - 0.9539 95.39%
Androgen receptor binding - 0.7911 79.11%
Thyroid receptor binding - 0.8366 83.66%
Glucocorticoid receptor binding - 0.9295 92.95%
Aromatase binding - 0.8092 80.92%
PPAR gamma - 0.6577 65.77%
Honey bee toxicity - 0.8615 86.15%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity - 0.6847 68.47%

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
CHEMBL2581 P07339 Cathepsin D 94.43% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.59% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 91.73% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.00% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.68% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.02% 86.33%
CHEMBL6007 O75762 Transient receptor potential cation channel subfamily A member 1 80.07% 92.17%

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 12339648
LOTUS LTS0274831
wikiData Q72485186