Perenniporide B

Details

Top
Internal ID aeca9cb8-79a4-4b94-995d-7d5570bc4490
Taxonomy Benzenoids > Naphthalenes
IUPAC Name methyl (2R)-3-[(1R)-6-ethyl-1,5-dihydroxy-2,7-dimethoxy-4-oxonaphthalen-1-yl]-2-hydroxypropanoate
SMILES (Canonical) CCC1=C(C=C2C(=C1O)C(=O)C=C(C2(CC(C(=O)OC)O)O)OC)OC
SMILES (Isomeric) CCC1=C(C=C2C(=C1O)C(=O)C=C([C@]2(C[C@H](C(=O)OC)O)O)OC)OC
InChI InChI=1S/C18H22O8/c1-5-9-13(24-2)6-10-15(16(9)21)11(19)7-14(25-3)18(10,23)8-12(20)17(22)26-4/h6-7,12,20-21,23H,5,8H2,1-4H3/t12-,18-/m1/s1
InChI Key WZZOARZEYMJHRI-KZULUSFZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C18H22O8
Molecular Weight 366.40 g/mol
Exact Mass 366.13146766 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 0.80
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

Top
CHEMBL2253040

2D Structure

Top
2D Structure of Perenniporide B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.6455 64.55%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5843 58.43%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.8212 82.12%
OATP1B3 inhibitior + 0.8866 88.66%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8438 84.38%
P-glycoprotein inhibitior - 0.7203 72.03%
P-glycoprotein substrate - 0.5958 59.58%
CYP3A4 substrate + 0.6072 60.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8569 85.69%
CYP3A4 inhibition - 0.8516 85.16%
CYP2C9 inhibition - 0.8339 83.39%
CYP2C19 inhibition - 0.8710 87.10%
CYP2D6 inhibition - 0.9181 91.81%
CYP1A2 inhibition - 0.7493 74.93%
CYP2C8 inhibition + 0.4772 47.72%
CYP inhibitory promiscuity - 0.7681 76.81%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9461 94.61%
Carcinogenicity (trinary) Non-required 0.5852 58.52%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.7127 71.27%
Skin irritation - 0.7156 71.56%
Skin corrosion - 0.9379 93.79%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4546 45.46%
Micronuclear + 0.5859 58.59%
Hepatotoxicity + 0.5450 54.50%
skin sensitisation - 0.6955 69.55%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8714 87.14%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6132 61.32%
Acute Oral Toxicity (c) III 0.5138 51.38%
Estrogen receptor binding + 0.8374 83.74%
Androgen receptor binding + 0.6894 68.94%
Thyroid receptor binding + 0.5707 57.07%
Glucocorticoid receptor binding + 0.8009 80.09%
Aromatase binding + 0.6156 61.56%
PPAR gamma + 0.7407 74.07%
Honey bee toxicity - 0.8501 85.01%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9776 97.76%

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 98.70% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.85% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.81% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.74% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.97% 96.09%
CHEMBL4208 P20618 Proteasome component C5 91.80% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.54% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.23% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.20% 95.56%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.24% 91.07%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.25% 90.71%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 85.22% 80.00%
CHEMBL221 P23219 Cyclooxygenase-1 84.54% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.07% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.50% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.38% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 82.25% 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 60199564
LOTUS LTS0029266
wikiData Q105323727