10-Bromo-beta-chamigrene

Details

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Internal ID da8d5044-0d02-4701-a2da-e13426910063
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Chamigranes
IUPAC Name (4R,6R)-4-bromo-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-ene
SMILES (Canonical) CC1=CCC2(CC1)C(=C)CCC(C2(C)C)Br
SMILES (Isomeric) CC1=CC[C@]2(CC1)C(=C)CC[C@H](C2(C)C)Br
InChI InChI=1S/C15H23Br/c1-11-7-9-15(10-8-11)12(2)5-6-13(16)14(15,3)4/h7,13H,2,5-6,8-10H2,1,3-4H3/t13-,15+/m1/s1
InChI Key ZATQJGNPERFQSF-HIFRSBDPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H23Br
Molecular Weight 283.25 g/mol
Exact Mass 282.09831 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 5.24
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Bromo-beta-chamigrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9874 98.74%
Caco-2 + 0.8844 88.44%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.7094 70.94%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.9278 92.78%
OATP1B3 inhibitior + 0.8122 81.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.6139 61.39%
P-glycoprotein inhibitior - 0.9481 94.81%
P-glycoprotein substrate - 0.9332 93.32%
CYP3A4 substrate + 0.5667 56.67%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7842 78.42%
CYP3A4 inhibition - 0.8461 84.61%
CYP2C9 inhibition - 0.6543 65.43%
CYP2C19 inhibition - 0.6520 65.20%
CYP2D6 inhibition - 0.9250 92.50%
CYP1A2 inhibition - 0.8184 81.84%
CYP2C8 inhibition - 0.8398 83.98%
CYP inhibitory promiscuity - 0.6078 60.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7513 75.13%
Carcinogenicity (trinary) Non-required 0.5556 55.56%
Eye corrosion - 0.9402 94.02%
Eye irritation + 0.5561 55.61%
Skin irritation - 0.6945 69.45%
Skin corrosion - 0.9571 95.71%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4015 40.15%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6430 64.30%
skin sensitisation + 0.6492 64.92%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.4747 47.47%
Acute Oral Toxicity (c) III 0.7383 73.83%
Estrogen receptor binding - 0.8806 88.06%
Androgen receptor binding - 0.5190 51.90%
Thyroid receptor binding - 0.7461 74.61%
Glucocorticoid receptor binding - 0.6403 64.03%
Aromatase binding - 0.6806 68.06%
PPAR gamma - 0.7372 73.72%
Honey bee toxicity - 0.7768 77.68%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.50% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.35% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.94% 91.11%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 88.86% 86.00%
CHEMBL1871 P10275 Androgen Receptor 88.39% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.18% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.36% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.27% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.79% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.70% 92.94%
CHEMBL2581 P07339 Cathepsin D 81.33% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 80.54% 94.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Eleutherococcus giraldii
Lespedeza davidii
Solanum aethiopicum
Tectona grandis

Cross-Links

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PubChem 21675030
NPASS NPC51743
LOTUS LTS0142799
wikiData Q105370106