19-Deoxyicetexone

Details

Top
Internal ID e7e4333a-9529-4751-9cc1-b6f073f4da2d
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name (1S,11S,12S)-7-hydroxy-12-methyl-6-propan-2-yl-16-oxatetracyclo[10.3.2.01,11.03,8]heptadeca-3(8),6,9-triene-4,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24O4/c1-11(2)15-16(21)12-5-6-14-19(3)7-4-8-20(14,24-10-19)9-13(12)17(22)18(15)23/h5-6,11,14,21H,4,7-10H2,1-3H3/t14-,19+,20-/m0/s1
InChI Key JOEFMVDPFYTOAT-KPOBHBOGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H24O4
Molecular Weight 328.40 g/mol
Exact Mass 328.16745924 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 2.30
Atomic LogP (AlogP) 3.44
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 19-Deoxyicetexone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.5776 57.76%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8368 83.68%
OATP2B1 inhibitior - 0.8591 85.91%
OATP1B1 inhibitior + 0.8548 85.48%
OATP1B3 inhibitior + 0.9807 98.07%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.8186 81.86%
BSEP inhibitior + 0.5739 57.39%
P-glycoprotein inhibitior - 0.8075 80.75%
P-glycoprotein substrate - 0.7028 70.28%
CYP3A4 substrate + 0.6083 60.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8751 87.51%
CYP3A4 inhibition - 0.9199 91.99%
CYP2C9 inhibition - 0.7775 77.75%
CYP2C19 inhibition - 0.8859 88.59%
CYP2D6 inhibition - 0.9408 94.08%
CYP1A2 inhibition - 0.6861 68.61%
CYP2C8 inhibition - 0.8438 84.38%
CYP inhibitory promiscuity - 0.9156 91.56%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4989 49.89%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.8840 88.40%
Skin irritation + 0.5390 53.90%
Skin corrosion - 0.9244 92.44%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7931 79.31%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.5334 53.34%
skin sensitisation - 0.8472 84.72%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.7744 77.44%
Acute Oral Toxicity (c) III 0.6796 67.96%
Estrogen receptor binding + 0.7442 74.42%
Androgen receptor binding + 0.6226 62.26%
Thyroid receptor binding + 0.5968 59.68%
Glucocorticoid receptor binding + 0.8099 80.99%
Aromatase binding + 0.5490 54.90%
PPAR gamma + 0.7871 78.71%
Honey bee toxicity - 0.7624 76.24%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9907 99.07%

Targets

Top

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 97.86% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.08% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.60% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 92.26% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.22% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.35% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.70% 97.25%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.87% 96.77%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.31% 93.40%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.26% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.59% 89.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.48% 93.04%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.43% 82.69%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.01% 90.71%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.30% 91.07%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.83% 98.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.47% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.36% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 80.57% 94.73%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 101936039
LOTUS LTS0140926
wikiData Q105132285