Asiaticusin B

Details

Top
Internal ID 0f73709b-c988-4a06-83c9-3240c0e9fce1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 3-[(2E,6E,10E,15Z)-16-carboxy-4,8,12-trimethylheptadeca-2,6,10,15-tetraenyl]-4-hydroxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H38O5/c1-20(9-5-11-21(2)13-7-15-23(4)27(30)31)10-6-12-22(3)14-8-16-24-19-25(28(32)33)17-18-26(24)29/h5-6,8,10-11,14-15,17-22,29H,7,9,12-13,16H2,1-4H3,(H,30,31)(H,32,33)/b10-6+,11-5+,14-8+,23-15-
InChI Key LPMYTILEFMOKDZ-SALQWAMYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C28H38O5
Molecular Weight 454.60 g/mol
Exact Mass 454.27192431 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 6.90
Atomic LogP (AlogP) 6.80
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 14

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Asiaticusin B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9817 98.17%
Caco-2 - 0.7459 74.59%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8660 86.60%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.8726 87.26%
OATP1B3 inhibitior + 0.8571 85.71%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9647 96.47%
P-glycoprotein inhibitior + 0.7150 71.50%
P-glycoprotein substrate - 0.7574 75.74%
CYP3A4 substrate - 0.5342 53.42%
CYP2C9 substrate + 0.6306 63.06%
CYP2D6 substrate - 0.8950 89.50%
CYP3A4 inhibition - 0.7510 75.10%
CYP2C9 inhibition - 0.5526 55.26%
CYP2C19 inhibition - 0.5214 52.14%
CYP2D6 inhibition - 0.6998 69.98%
CYP1A2 inhibition + 0.6621 66.21%
CYP2C8 inhibition - 0.6335 63.35%
CYP inhibitory promiscuity - 0.7397 73.97%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7277 72.77%
Carcinogenicity (trinary) Non-required 0.7106 71.06%
Eye corrosion - 0.9865 98.65%
Eye irritation - 0.9360 93.60%
Skin irritation - 0.6698 66.98%
Skin corrosion - 0.9021 90.21%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7608 76.08%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.4884 48.84%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7395 73.95%
Acute Oral Toxicity (c) III 0.5496 54.96%
Estrogen receptor binding + 0.7180 71.80%
Androgen receptor binding + 0.5439 54.39%
Thyroid receptor binding + 0.6169 61.69%
Glucocorticoid receptor binding + 0.6358 63.58%
Aromatase binding + 0.5499 54.99%
PPAR gamma + 0.7073 70.73%
Honey bee toxicity - 0.9135 91.35%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 1.0000 100.00%

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 97.17% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 93.21% 91.49%
CHEMBL2581 P07339 Cathepsin D 92.40% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.07% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.12% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 90.11% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.80% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.40% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.08% 86.33%
CHEMBL3194 P02766 Transthyretin 85.71% 90.71%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.49% 100.00%
CHEMBL2535 P11166 Glucose transporter 82.40% 98.75%
CHEMBL340 P08684 Cytochrome P450 3A4 80.97% 91.19%

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 139584601
LOTUS LTS0174513
wikiData Q77372193