4-Chloro-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enylidene)-2,3,4,5,7,7a-hexahydro-1-benzofuran-3a,5-diol

Details

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Internal ID 99a0e04d-a0c9-4447-aa54-0a0be52dec08
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 4-chloro-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enylidene)-2,3,4,5,7,7a-hexahydro-1-benzofuran-3a,5-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H25ClO4/c1-9(2)5-6-10-7-11-16(20,14(17)13(10)18)8-12(21-11)15(3,4)19/h5-6,11-14,18-20H,7-8H2,1-4H3
InChI Key XLJUPGGTLAFLOF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H25ClO4
Molecular Weight 316.82 g/mol
Exact Mass 316.1441370 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.91
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Chloro-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enylidene)-2,3,4,5,7,7a-hexahydro-1-benzofuran-3a,5-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9853 98.53%
Caco-2 - 0.6046 60.46%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5894 58.94%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.9144 91.44%
OATP1B3 inhibitior + 0.9487 94.87%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8602 86.02%
P-glycoprotein inhibitior - 0.8946 89.46%
P-glycoprotein substrate - 0.7712 77.12%
CYP3A4 substrate + 0.5930 59.30%
CYP2C9 substrate - 0.7995 79.95%
CYP2D6 substrate - 0.7774 77.74%
CYP3A4 inhibition - 0.9550 95.50%
CYP2C9 inhibition - 0.8314 83.14%
CYP2C19 inhibition - 0.7817 78.17%
CYP2D6 inhibition - 0.8992 89.92%
CYP1A2 inhibition - 0.8164 81.64%
CYP2C8 inhibition - 0.7726 77.26%
CYP inhibitory promiscuity - 0.6323 63.23%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8638 86.38%
Carcinogenicity (trinary) Non-required 0.4438 44.38%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.9810 98.10%
Skin irritation - 0.6379 63.79%
Skin corrosion - 0.9059 90.59%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5657 56.57%
Micronuclear - 0.7341 73.41%
Hepatotoxicity - 0.5176 51.76%
skin sensitisation - 0.7454 74.54%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.5618 56.18%
Acute Oral Toxicity (c) III 0.3703 37.03%
Estrogen receptor binding + 0.7184 71.84%
Androgen receptor binding - 0.5921 59.21%
Thyroid receptor binding + 0.6180 61.80%
Glucocorticoid receptor binding + 0.6275 62.75%
Aromatase binding - 0.5064 50.64%
PPAR gamma + 0.5727 57.27%
Honey bee toxicity - 0.7683 76.83%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9751 97.51%

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 95.38% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.96% 94.45%
CHEMBL226 P30542 Adenosine A1 receptor 90.48% 95.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.12% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.61% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 84.88% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.72% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.94% 89.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.54% 100.00%
CHEMBL1977 P11473 Vitamin D receptor 80.88% 99.43%

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 139583937
LOTUS LTS0236293
wikiData Q75069472