5-Hydroxymethyl isochroman-1-one

Details

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Internal ID b5ea957b-0dd6-429f-b53c-601506685839
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 5-(hydroxymethyl)-3,4-dihydroisochromen-1-one
SMILES (Canonical) C1COC(=O)C2=CC=CC(=C21)CO
SMILES (Isomeric) C1COC(=O)C2=CC=CC(=C21)CO
InChI InChI=1S/C10H10O3/c11-6-7-2-1-3-9-8(7)4-5-13-10(9)12/h1-3,11H,4-6H2
InChI Key DNNSYXUCMMUSNY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H10O3
Molecular Weight 178.18 g/mol
Exact Mass 178.062994177 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.89
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL3397162
5-Hydroxymethyl isochroman-1-one

2D Structure

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2D Structure of 5-Hydroxymethyl isochroman-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9675 96.75%
Caco-2 + 0.7831 78.31%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6929 69.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9593 95.93%
OATP1B3 inhibitior + 0.9575 95.75%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8519 85.19%
P-glycoprotein inhibitior - 0.9752 97.52%
P-glycoprotein substrate - 0.9444 94.44%
CYP3A4 substrate - 0.5659 56.59%
CYP2C9 substrate - 0.8005 80.05%
CYP2D6 substrate - 0.7967 79.67%
CYP3A4 inhibition - 0.9213 92.13%
CYP2C9 inhibition - 0.6395 63.95%
CYP2C19 inhibition + 0.6326 63.26%
CYP2D6 inhibition - 0.8523 85.23%
CYP1A2 inhibition - 0.6692 66.92%
CYP2C8 inhibition - 0.9446 94.46%
CYP inhibitory promiscuity - 0.9059 90.59%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6629 66.29%
Eye corrosion - 0.9375 93.75%
Eye irritation + 0.9965 99.65%
Skin irritation - 0.8271 82.71%
Skin corrosion - 0.9713 97.13%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6937 69.37%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5902 59.02%
skin sensitisation - 0.8330 83.30%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.5775 57.75%
Acute Oral Toxicity (c) III 0.6186 61.86%
Estrogen receptor binding - 0.7001 70.01%
Androgen receptor binding + 0.5871 58.71%
Thyroid receptor binding - 0.7583 75.83%
Glucocorticoid receptor binding - 0.8911 89.11%
Aromatase binding - 0.8626 86.26%
PPAR gamma - 0.6038 60.38%
Honey bee toxicity - 0.9465 94.65%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.7263 72.63%

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 95.87% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.67% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.77% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.41% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.61% 92.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.77% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.69% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.00% 97.25%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.18% 96.77%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.10% 98.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Swertia japonica

Cross-Links

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PubChem 23725722
NPASS NPC306740
LOTUS LTS0227875
wikiData Q104985654