10-Bromo-obtusallene

Details

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Internal ID 1ef75e04-2f97-40ee-b17e-2d7324491b8d
Taxonomy Organohalogen compounds > Vinyl halides > Vinyl bromides
IUPAC Name (1S,2S,4S,5Z,7R,12S)-10-bromo-4-(3-bromopropa-1,2-dienyl)-7-chloro-2,12-dimethyl-3,13-dioxabicyclo[7.3.1]trideca-5,9-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H19Br2ClO2/c1-10-8-14(18)15-9-12(19)5-6-13(4-3-7-17)20-11(2)16(10)21-15/h4-7,10-13,16H,8-9H2,1-2H3/b6-5-/t3?,10-,11-,12-,13+,16-/m0/s1
InChI Key WBFNLWIUNUWBSX-XYTKKIMDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H19Br2ClO2
Molecular Weight 438.60 g/mol
Exact Mass 437.94198 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 4.30
Atomic LogP (AlogP) 5.42
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Bromo-obtusallene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.6682 66.82%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.4730 47.30%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.8521 85.21%
OATP1B3 inhibitior + 0.9521 95.21%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8004 80.04%
P-glycoprotein inhibitior - 0.8575 85.75%
P-glycoprotein substrate - 0.7395 73.95%
CYP3A4 substrate + 0.5508 55.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8020 80.20%
CYP3A4 inhibition - 0.6174 61.74%
CYP2C9 inhibition - 0.7080 70.80%
CYP2C19 inhibition - 0.5881 58.81%
CYP2D6 inhibition - 0.8724 87.24%
CYP1A2 inhibition - 0.5684 56.84%
CYP2C8 inhibition - 0.7975 79.75%
CYP inhibitory promiscuity - 0.6576 65.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.5674 56.74%
Eye corrosion - 0.8977 89.77%
Eye irritation - 0.9939 99.39%
Skin irritation - 0.5792 57.92%
Skin corrosion - 0.8843 88.43%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7771 77.71%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.5197 51.97%
skin sensitisation - 0.5433 54.33%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.7521 75.21%
Acute Oral Toxicity (c) III 0.6180 61.80%
Estrogen receptor binding + 0.6448 64.48%
Androgen receptor binding - 0.5569 55.69%
Thyroid receptor binding + 0.5668 56.68%
Glucocorticoid receptor binding + 0.6208 62.08%
Aromatase binding - 0.5087 50.87%
PPAR gamma + 0.5924 59.24%
Honey bee toxicity - 0.5766 57.66%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.8229 82.29%

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 93.18% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.46% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.43% 94.73%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.37% 86.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.26% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.74% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 81.11% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.87% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 80.69% 91.49%

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 139586321
LOTUS LTS0143160
wikiData Q77504027