Clearanol H

Details

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Internal ID 6dc5f5cb-f7d0-4ed9-a453-abc03a97d9bc
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (4S)-8-hydroxy-5-(hydroxymethyl)-6-methoxy-4-methyl-3-methylidene-4H-isochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14O5/c1-6-7(2)18-13(16)12-9(15)4-10(17-3)8(5-14)11(6)12/h4,6,14-15H,2,5H2,1,3H3/t6-/m1/s1
InChI Key XADJGPTUFXXSOG-ZCFIWIBFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O5
Molecular Weight 250.25 g/mol
Exact Mass 250.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Clearanol H

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9630 96.30%
Caco-2 - 0.6260 62.60%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7421 74.21%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.7944 79.44%
OATP1B3 inhibitior + 0.9271 92.71%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9478 94.78%
P-glycoprotein inhibitior - 0.8889 88.89%
P-glycoprotein substrate - 0.8704 87.04%
CYP3A4 substrate + 0.5143 51.43%
CYP2C9 substrate + 0.6220 62.20%
CYP2D6 substrate - 0.8495 84.95%
CYP3A4 inhibition + 0.5729 57.29%
CYP2C9 inhibition + 0.5250 52.50%
CYP2C19 inhibition + 0.7292 72.92%
CYP2D6 inhibition - 0.8326 83.26%
CYP1A2 inhibition + 0.6272 62.72%
CYP2C8 inhibition - 0.6521 65.21%
CYP inhibitory promiscuity + 0.8315 83.15%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9231 92.31%
Carcinogenicity (trinary) Non-required 0.7237 72.37%
Eye corrosion - 0.9749 97.49%
Eye irritation - 0.5902 59.02%
Skin irritation - 0.7524 75.24%
Skin corrosion - 0.9624 96.24%
Ames mutagenesis + 0.5664 56.64%
Human Ether-a-go-go-Related Gene inhibition - 0.7342 73.42%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.6999 69.99%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7869 78.69%
Acute Oral Toxicity (c) III 0.5117 51.17%
Estrogen receptor binding - 0.6051 60.51%
Androgen receptor binding - 0.5534 55.34%
Thyroid receptor binding + 0.5550 55.50%
Glucocorticoid receptor binding - 0.5453 54.53%
Aromatase binding - 0.4892 48.92%
PPAR gamma + 0.6481 64.81%
Honey bee toxicity - 0.8569 85.69%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9605 96.05%

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 97.41% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.98% 93.99%
CHEMBL2581 P07339 Cathepsin D 93.75% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.24% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.11% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.77% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.98% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.35% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.06% 99.17%
CHEMBL4208 P20618 Proteasome component C5 80.88% 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 132576836
LOTUS LTS0228641
wikiData Q105323858