3-(4-Hydroxy-4-methylpentyl)-3-methyl-1,2-benzodioxole-6-carboxylic acid

Details

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Internal ID 9d48868f-91a6-4c35-a30b-f68604e62e03
Taxonomy Benzenoids
IUPAC Name 3-(4-hydroxy-4-methylpentyl)-3-methyl-1,2-benzodioxole-6-carboxylic acid
SMILES (Canonical) CC1(C2=C(C=C(C=C2)C(=O)O)OO1)CCCC(C)(C)O
SMILES (Isomeric) CC1(C2=C(C=C(C=C2)C(=O)O)OO1)CCCC(C)(C)O
InChI InChI=1S/C15H20O5/c1-14(2,18)7-4-8-15(3)11-6-5-10(13(16)17)9-12(11)19-20-15/h5-6,9,18H,4,7-8H2,1-3H3,(H,16,17)
InChI Key VPUMRTLIHAHBNQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O5
Molecular Weight 280.32 g/mol
Exact Mass 280.13107373 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4-Hydroxy-4-methylpentyl)-3-methyl-1,2-benzodioxole-6-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9832 98.32%
Caco-2 + 0.7733 77.33%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6818 68.18%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.8783 87.83%
OATP1B3 inhibitior + 0.8951 89.51%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7468 74.68%
P-glycoprotein inhibitior - 0.9526 95.26%
P-glycoprotein substrate - 0.8017 80.17%
CYP3A4 substrate - 0.5192 51.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8593 85.93%
CYP3A4 inhibition - 0.8062 80.62%
CYP2C9 inhibition - 0.7971 79.71%
CYP2C19 inhibition - 0.8257 82.57%
CYP2D6 inhibition - 0.9111 91.11%
CYP1A2 inhibition - 0.5860 58.60%
CYP2C8 inhibition + 0.6427 64.27%
CYP inhibitory promiscuity - 0.8526 85.26%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.5370 53.70%
Eye corrosion - 0.9798 97.98%
Eye irritation - 0.6022 60.22%
Skin irritation - 0.6837 68.37%
Skin corrosion - 0.8837 88.37%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5757 57.57%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.6073 60.73%
skin sensitisation - 0.7367 73.67%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4624 46.24%
Acute Oral Toxicity (c) III 0.5067 50.67%
Estrogen receptor binding + 0.8171 81.71%
Androgen receptor binding - 0.5715 57.15%
Thyroid receptor binding + 0.6056 60.56%
Glucocorticoid receptor binding - 0.5287 52.87%
Aromatase binding + 0.6408 64.08%
PPAR gamma + 0.7551 75.51%
Honey bee toxicity - 0.9641 96.41%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7252 72.52%
Fish aquatic toxicity + 0.9444 94.44%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.00% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.25% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.14% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.42% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.67% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.67% 99.17%
CHEMBL4208 P20618 Proteasome component C5 87.07% 90.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 83.44% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.96% 81.11%

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 162849599
LOTUS LTS0058342
wikiData Q104199683