Bca 11

Details

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Internal ID 1e0b7c9f-a196-4920-8744-0f001727ca6c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3-hydroxy-2-[[5-hydroxy-2-(7-hydroxy-6-methylheptan-2-yl)-5-methylcyclopent-2-en-1-yl]methyl]-4-methoxycyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H36O5/c1-14(13-23)6-5-7-15(2)16-10-11-22(3,26)18(16)12-17-19(24)8-9-20(27-4)21(17)25/h10,14-15,18,20,23,25-26H,5-9,11-13H2,1-4H3
InChI Key CNCWASXFRPCBBE-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H36O5
Molecular Weight 380.50 g/mol
Exact Mass 380.25627424 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Bca 11

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9797 97.97%
Caco-2 + 0.6963 69.63%
Blood Brain Barrier + 0.7635 76.35%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8364 83.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9159 91.59%
OATP1B3 inhibitior + 0.9352 93.52%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior + 0.5232 52.32%
BSEP inhibitior + 0.5731 57.31%
P-glycoprotein inhibitior - 0.6056 60.56%
P-glycoprotein substrate - 0.5642 56.42%
CYP3A4 substrate + 0.6694 66.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8820 88.20%
CYP3A4 inhibition - 0.8755 87.55%
CYP2C9 inhibition - 0.7730 77.30%
CYP2C19 inhibition - 0.8376 83.76%
CYP2D6 inhibition - 0.9278 92.78%
CYP1A2 inhibition - 0.8364 83.64%
CYP2C8 inhibition - 0.6647 66.47%
CYP inhibitory promiscuity - 0.9361 93.61%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9128 91.28%
Carcinogenicity (trinary) Non-required 0.6811 68.11%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.9243 92.43%
Skin irritation - 0.5973 59.73%
Skin corrosion - 0.9762 97.62%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6777 67.77%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5286 52.86%
skin sensitisation - 0.8570 85.70%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.4886 48.86%
Acute Oral Toxicity (c) III 0.4650 46.50%
Estrogen receptor binding + 0.7671 76.71%
Androgen receptor binding - 0.5858 58.58%
Thyroid receptor binding + 0.6480 64.80%
Glucocorticoid receptor binding + 0.8353 83.53%
Aromatase binding - 0.4909 49.09%
PPAR gamma + 0.6663 66.63%
Honey bee toxicity - 0.8951 89.51%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5507 55.07%
Fish aquatic toxicity + 0.8879 88.79%

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 98.76% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.11% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 97.80% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.56% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.24% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.46% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.53% 82.69%
CHEMBL1937 Q92769 Histone deacetylase 2 89.36% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.19% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.08% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.49% 93.99%
CHEMBL2996 Q05655 Protein kinase C delta 85.86% 97.79%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.86% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.73% 99.17%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.58% 92.88%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.79% 92.94%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.41% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.11% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.47% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.07% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 80.61% 95.93%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.47% 97.33%

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 139587962
LOTUS LTS0118803
wikiData Q103817881