(3R,4R)-4,8-dihydroxy-5-(hydroxymethyl)-3-methylisochroman-1-one

Details

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Internal ID 004fc968-778f-4372-bd10-12f2b5d8b08c
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3R,4S)-4,8-dihydroxy-5-(hydroxymethyl)-3-methyl-3,4-dihydroisochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O5/c1-5-10(14)8-6(4-12)2-3-7(13)9(8)11(15)16-5/h2-3,5,10,12-14H,4H2,1H3/t5-,10-/m1/s1
InChI Key ZHWRNRQCZZTGIO-GPXNAGAYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O5
Molecular Weight 224.21 g/mol
Exact Mass 224.06847348 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.48
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,4R)-4,8-dihydroxy-5-(hydroxymethyl)-3-methylisochroman-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 + 0.8816 88.16%
Caco-2 - 0.8478 84.78%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7320 73.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8870 88.70%
OATP1B3 inhibitior + 0.9532 95.32%
MATE1 inhibitior - 0.6400 64.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9705 97.05%
P-glycoprotein inhibitior - 0.9409 94.09%
P-glycoprotein substrate - 0.9335 93.35%
CYP3A4 substrate - 0.5443 54.43%
CYP2C9 substrate - 0.5773 57.73%
CYP2D6 substrate - 0.8547 85.47%
CYP3A4 inhibition - 0.8763 87.63%
CYP2C9 inhibition + 0.5827 58.27%
CYP2C19 inhibition - 0.8011 80.11%
CYP2D6 inhibition - 0.9274 92.74%
CYP1A2 inhibition - 0.5580 55.80%
CYP2C8 inhibition - 0.9301 93.01%
CYP inhibitory promiscuity - 0.5276 52.76%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6938 69.38%
Eye corrosion - 0.9817 98.17%
Eye irritation + 0.5859 58.59%
Skin irritation - 0.6225 62.25%
Skin corrosion - 0.9517 95.17%
Ames mutagenesis + 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7601 76.01%
Micronuclear + 0.5774 57.74%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8434 84.34%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6439 64.39%
Acute Oral Toxicity (c) III 0.4119 41.19%
Estrogen receptor binding - 0.5194 51.94%
Androgen receptor binding - 0.5061 50.61%
Thyroid receptor binding - 0.7268 72.68%
Glucocorticoid receptor binding + 0.5968 59.68%
Aromatase binding - 0.8390 83.90%
PPAR gamma - 0.6977 69.77%
Honey bee toxicity - 0.9350 93.50%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.7777 77.77%

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 97.76% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.78% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.14% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.96% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 85.53% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.16% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.96% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.44% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.65% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 81.41% 91.49%

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 139591348
LOTUS LTS0133960
wikiData Q105376074