(4R,5aR,9S,9aS)-7-bromo-6,6,9a-trimethyl-4-prop-1-en-2-yl-4,5,5a,9-tetrahydro-1,3-benzodioxepin-9-ol

Details

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Internal ID c0686057-1dad-4f89-b4b9-abcb0c2bbf6f
Taxonomy Organoheterocyclic compounds > Dioxepanes > 1,3-dioxepanes
IUPAC Name (4R,5aR,9S,9aS)-7-bromo-6,6,9a-trimethyl-4-prop-1-en-2-yl-4,5,5a,9-tetrahydro-1,3-benzodioxepin-9-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H23BrO3/c1-9(2)10-6-11-14(3,4)12(16)7-13(17)15(11,5)19-8-18-10/h7,10-11,13,17H,1,6,8H2,2-5H3/t10-,11-,13+,15+/m1/s1
InChI Key WEXKOQISSZMUMG-ZSEWYUTFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H23BrO3
Molecular Weight 331.24 g/mol
Exact Mass 330.08306 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.38
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R,5aR,9S,9aS)-7-bromo-6,6,9a-trimethyl-4-prop-1-en-2-yl-4,5,5a,9-tetrahydro-1,3-benzodioxepin-9-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9812 98.12%
Caco-2 + 0.6372 63.72%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.5743 57.43%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.8822 88.22%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7193 71.93%
P-glycoprotein inhibitior - 0.9132 91.32%
P-glycoprotein substrate - 0.7694 76.94%
CYP3A4 substrate + 0.5695 56.95%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7596 75.96%
CYP3A4 inhibition - 0.6966 69.66%
CYP2C9 inhibition - 0.7820 78.20%
CYP2C19 inhibition - 0.7646 76.46%
CYP2D6 inhibition - 0.8998 89.98%
CYP1A2 inhibition - 0.7247 72.47%
CYP2C8 inhibition - 0.8152 81.52%
CYP inhibitory promiscuity - 0.8478 84.78%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8316 83.16%
Carcinogenicity (trinary) Non-required 0.5162 51.62%
Eye corrosion - 0.9788 97.88%
Eye irritation - 0.7070 70.70%
Skin irritation - 0.6638 66.38%
Skin corrosion - 0.9225 92.25%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4796 47.96%
Micronuclear - 0.6282 62.82%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.6888 68.88%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5735 57.35%
Acute Oral Toxicity (c) III 0.6081 60.81%
Estrogen receptor binding - 0.5128 51.28%
Androgen receptor binding - 0.6408 64.08%
Thyroid receptor binding + 0.5371 53.71%
Glucocorticoid receptor binding - 0.4796 47.96%
Aromatase binding - 0.5099 50.99%
PPAR gamma - 0.5561 55.61%
Honey bee toxicity - 0.7771 77.71%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9914 99.14%

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 97.59% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.53% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.52% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.99% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.73% 100.00%
CHEMBL2581 P07339 Cathepsin D 80.65% 98.95%

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 162961076
LOTUS LTS0216973
wikiData Q105303648