6-bromo-5,5-dimethyl-3,6,7,7a-tetrahydro-2H-1-benzofuran-3-ol

Details

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Internal ID 853839ca-a3f8-4d6f-815a-8a4624fd9672
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 6-bromo-5,5-dimethyl-3,6,7,7a-tetrahydro-2H-1-benzofuran-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H15BrO2/c1-10(2)4-6-7(12)5-13-8(6)3-9(10)11/h4,7-9,12H,3,5H2,1-2H3
InChI Key HNULJAOABSCBIT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H15BrO2
Molecular Weight 247.13 g/mol
Exact Mass 246.02554 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.87
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-bromo-5,5-dimethyl-3,6,7,7a-tetrahydro-2H-1-benzofuran-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.4919 49.19%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5371 53.71%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.9262 92.62%
OATP1B3 inhibitior + 0.9672 96.72%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9615 96.15%
P-glycoprotein inhibitior - 0.9618 96.18%
P-glycoprotein substrate - 0.9213 92.13%
CYP3A4 substrate + 0.5155 51.55%
CYP2C9 substrate - 0.6079 60.79%
CYP2D6 substrate - 0.7464 74.64%
CYP3A4 inhibition - 0.9632 96.32%
CYP2C9 inhibition - 0.7849 78.49%
CYP2C19 inhibition - 0.7318 73.18%
CYP2D6 inhibition - 0.8784 87.84%
CYP1A2 inhibition - 0.7146 71.46%
CYP2C8 inhibition - 0.9338 93.38%
CYP inhibitory promiscuity - 0.6538 65.38%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8551 85.51%
Carcinogenicity (trinary) Non-required 0.4394 43.94%
Eye corrosion - 0.9728 97.28%
Eye irritation + 0.6737 67.37%
Skin irritation - 0.6547 65.47%
Skin corrosion - 0.9192 91.92%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6464 64.64%
Micronuclear - 0.7241 72.41%
Hepatotoxicity + 0.6075 60.75%
skin sensitisation - 0.6983 69.83%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.5607 56.07%
Acute Oral Toxicity (c) III 0.5431 54.31%
Estrogen receptor binding - 0.7265 72.65%
Androgen receptor binding - 0.8132 81.32%
Thyroid receptor binding - 0.6918 69.18%
Glucocorticoid receptor binding - 0.5786 57.86%
Aromatase binding - 0.8877 88.77%
PPAR gamma - 0.7546 75.46%
Honey bee toxicity - 0.7713 77.13%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9539 95.39%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.29% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.16% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.29% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.00% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.13% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.87% 89.00%

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 73799038
LOTUS LTS0156199
wikiData Q105031074