Coleophomone B

Details

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Internal ID 904d8f69-8d2d-4b53-be49-6fe17ac04427
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name (11Z,14S)-2-hydroxy-11,15-dimethyl-14-(3-methylbut-2-enyl)-17,18-dioxo-9-oxatricyclo[12.3.1.03,8]octadeca-1,3,5,7,11,15-hexaene-4-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H26O5/c1-15(2)8-10-25-11-9-16(3)14-30-20-7-5-6-18(13-26)21(20)23(28)22(24(25)29)19(27)12-17(25)4/h5-9,12-13,28H,10-11,14H2,1-4H3/b16-9-,23-22?/t25-/m0/s1
InChI Key QUJTZZOLLMVPJC-WVWOERFASA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C25H26O5
Molecular Weight 406.50 g/mol
Exact Mass 406.17802393 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 3.50
Atomic LogP (AlogP) 4.94
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Coleophomone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.7240 72.40%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8410 84.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8575 85.75%
OATP1B3 inhibitior + 0.9374 93.74%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9352 93.52%
P-glycoprotein inhibitior + 0.5864 58.64%
P-glycoprotein substrate - 0.5755 57.55%
CYP3A4 substrate + 0.6414 64.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8433 84.33%
CYP3A4 inhibition - 0.6787 67.87%
CYP2C9 inhibition + 0.7349 73.49%
CYP2C19 inhibition + 0.6465 64.65%
CYP2D6 inhibition - 0.8171 81.71%
CYP1A2 inhibition + 0.8363 83.63%
CYP2C8 inhibition - 0.5613 56.13%
CYP inhibitory promiscuity + 0.6055 60.55%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8913 89.13%
Carcinogenicity (trinary) Non-required 0.6325 63.25%
Eye corrosion - 0.9872 98.72%
Eye irritation - 0.7796 77.96%
Skin irritation - 0.7088 70.88%
Skin corrosion - 0.9465 94.65%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6466 64.66%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.7427 74.27%
skin sensitisation - 0.6447 64.47%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.9336 93.36%
Acute Oral Toxicity (c) III 0.6319 63.19%
Estrogen receptor binding + 0.6752 67.52%
Androgen receptor binding + 0.7782 77.82%
Thyroid receptor binding - 0.5201 52.01%
Glucocorticoid receptor binding + 0.7799 77.99%
Aromatase binding + 0.6177 61.77%
PPAR gamma + 0.7841 78.41%
Honey bee toxicity - 0.8487 84.87%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5900 59.00%
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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.10% 94.45%
CHEMBL2581 P07339 Cathepsin D 96.99% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.58% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.38% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 94.64% 94.73%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.31% 93.40%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.03% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.55% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.92% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.92% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.70% 85.14%
CHEMBL3310 Q96DB2 Histone deacetylase 11 85.24% 88.56%
CHEMBL240 Q12809 HERG 85.16% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.35% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.62% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.70% 94.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.51% 94.80%

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 101204013
LOTUS LTS0161625
wikiData Q105228228