(3R,6Z)-6-(bromomethylidene)-3-chloro-2-methylocta-1,7-diene

Details

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Internal ID fdee5824-7c2c-4b33-81a5-01b737a1c95c
Taxonomy Organohalogen compounds > Vinyl halides > Vinyl bromides
IUPAC Name (3R,6Z)-6-(bromomethylidene)-3-chloro-2-methylocta-1,7-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14BrCl/c1-4-9(7-11)5-6-10(12)8(2)3/h4,7,10H,1-2,5-6H2,3H3/b9-7+/t10-/m1/s1
InChI Key OGYXYZYGQVDGED-TTZKWOQHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14BrCl
Molecular Weight 249.57 g/mol
Exact Mass 247.99674 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.41
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,6Z)-6-(bromomethylidene)-3-chloro-2-methylocta-1,7-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 + 0.7018 70.18%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.5413 54.13%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9072 90.72%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7908 79.08%
P-glycoprotein inhibitior - 0.9763 97.63%
P-glycoprotein substrate - 0.9152 91.52%
CYP3A4 substrate - 0.5696 56.96%
CYP2C9 substrate + 0.5655 56.55%
CYP2D6 substrate - 0.7835 78.35%
CYP3A4 inhibition - 0.9209 92.09%
CYP2C9 inhibition - 0.8046 80.46%
CYP2C19 inhibition - 0.6944 69.44%
CYP2D6 inhibition - 0.9045 90.45%
CYP1A2 inhibition - 0.6465 64.65%
CYP2C8 inhibition - 0.8994 89.94%
CYP inhibitory promiscuity - 0.6488 64.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5033 50.33%
Carcinogenicity (trinary) Non-required 0.5086 50.86%
Eye corrosion + 0.7649 76.49%
Eye irritation + 0.6113 61.13%
Skin irritation + 0.6741 67.41%
Skin corrosion + 0.6478 64.78%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.6748 67.48%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.7881 78.81%
Acute Oral Toxicity (c) III 0.7961 79.61%
Estrogen receptor binding - 0.8583 85.83%
Androgen receptor binding - 0.8614 86.14%
Thyroid receptor binding - 0.8057 80.57%
Glucocorticoid receptor binding + 0.5986 59.86%
Aromatase binding - 0.6995 69.95%
PPAR gamma + 0.5277 52.77%
Honey bee toxicity - 0.4654 46.54%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9709 97.09%

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
CHEMBL2581 P07339 Cathepsin D 88.50% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.06% 96.09%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 85.74% 97.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.38% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 82.22% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 81.66% 94.73%
CHEMBL3587 Q02750 Dual specificity mitogen-activated protein kinase kinase 1 81.64% 97.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.86% 99.17%

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 162885923
LOTUS LTS0115652
wikiData Q105191946