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

Details

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Internal ID e8e24074-cb8a-41e5-8b95-a257206ca87d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (3Z)-2-bromo-3-(bromomethylidene)-6-chloro-7-methylocta-1,6-diene
SMILES (Canonical) CC(=C(CCC(=CBr)C(=C)Br)Cl)C
SMILES (Isomeric) CC(=C(CC/C(=C/Br)/C(=C)Br)Cl)C
InChI InChI=1S/C10H13Br2Cl/c1-7(2)10(13)5-4-9(6-11)8(3)12/h6H,3-5H2,1-2H3/b9-6-
InChI Key AKXLQPIDMZTIOB-TWGQIWQCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H13Br2Cl
Molecular Weight 328.47 g/mol
Exact Mass 327.90520 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.49
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 + 0.8296 82.96%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Nucleus 0.4501 45.01%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.8989 89.89%
OATP1B3 inhibitior + 0.9364 93.64%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6484 64.84%
P-glycoprotein inhibitior - 0.9589 95.89%
P-glycoprotein substrate - 0.9310 93.10%
CYP3A4 substrate - 0.5611 56.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7749 77.49%
CYP3A4 inhibition - 0.9491 94.91%
CYP2C9 inhibition - 0.8074 80.74%
CYP2C19 inhibition - 0.7053 70.53%
CYP2D6 inhibition - 0.9001 90.01%
CYP1A2 inhibition - 0.7082 70.82%
CYP2C8 inhibition - 0.9086 90.86%
CYP inhibitory promiscuity - 0.7136 71.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5253 52.53%
Carcinogenicity (trinary) Non-required 0.5255 52.55%
Eye corrosion + 0.6475 64.75%
Eye irritation + 0.8667 86.67%
Skin irritation + 0.6790 67.90%
Skin corrosion - 0.5711 57.11%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5830 58.30%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6177 61.77%
skin sensitisation + 0.7385 73.85%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.7580 75.80%
Acute Oral Toxicity (c) III 0.7547 75.47%
Estrogen receptor binding - 0.8089 80.89%
Androgen receptor binding - 0.7048 70.48%
Thyroid receptor binding - 0.7553 75.53%
Glucocorticoid receptor binding - 0.5288 52.88%
Aromatase binding + 0.5213 52.13%
PPAR gamma + 0.6960 69.60%
Honey bee toxicity - 0.7964 79.64%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9808 98.08%

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
CHEMBL240 Q12809 HERG 96.40% 89.76%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.69% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.74% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.49% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.06% 97.25%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.53% 96.95%

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 23424594
LOTUS LTS0063284
wikiData Q104913911