Sollasin B

Details

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Internal ID 98159362-f91d-4f1c-8239-21fba49b524f
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-acyl-alpha amino acids and derivatives
IUPAC Name (E)-3-methyl-N-[(3R)-2-oxopiperidin-3-yl]-5-[(1S,6R)-1,2,6-trimethylcyclohex-2-en-1-yl]pent-2-enamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32N2O2/c1-14(10-11-20(4)15(2)7-5-8-16(20)3)13-18(23)22-17-9-6-12-21-19(17)24/h7,13,16-17H,5-6,8-12H2,1-4H3,(H,21,24)(H,22,23)/b14-13+/t16-,17-,20-/m1/s1
InChI Key AETOKBXKVBFSTR-VBRACAIISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32N2O2
Molecular Weight 332.50 g/mol
Exact Mass 332.246378268 g/mol
Topological Polar Surface Area (TPSA) 58.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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CHEMBL483421

2D Structure

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2D Structure of Sollasin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9517 95.17%
Caco-2 - 0.5975 59.75%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5106 51.06%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.9078 90.78%
OATP1B3 inhibitior + 0.9377 93.77%
MATE1 inhibitior - 0.8454 84.54%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6063 60.63%
P-glycoprotein inhibitior - 0.6301 63.01%
P-glycoprotein substrate + 0.6065 60.65%
CYP3A4 substrate + 0.6134 61.34%
CYP2C9 substrate + 0.5471 54.71%
CYP2D6 substrate - 0.9026 90.26%
CYP3A4 inhibition - 0.8102 81.02%
CYP2C9 inhibition - 0.6967 69.67%
CYP2C19 inhibition - 0.6307 63.07%
CYP2D6 inhibition - 0.8958 89.58%
CYP1A2 inhibition - 0.9240 92.40%
CYP2C8 inhibition - 0.7353 73.53%
CYP inhibitory promiscuity - 0.8726 87.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5885 58.85%
Eye corrosion - 0.9781 97.81%
Eye irritation - 0.9802 98.02%
Skin irritation - 0.7445 74.45%
Skin corrosion - 0.9182 91.82%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7693 76.93%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8496 84.96%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7664 76.64%
Acute Oral Toxicity (c) III 0.6357 63.57%
Estrogen receptor binding + 0.5366 53.66%
Androgen receptor binding + 0.5920 59.20%
Thyroid receptor binding + 0.6771 67.71%
Glucocorticoid receptor binding + 0.6861 68.61%
Aromatase binding + 0.5869 58.69%
PPAR gamma + 0.7967 79.67%
Honey bee toxicity - 0.9166 91.66%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.8768 87.68%

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
CHEMBL2581 P07339 Cathepsin D 94.67% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.57% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.15% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.46% 97.25%
CHEMBL4208 P20618 Proteasome component C5 91.85% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.57% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 90.42% 93.03%
CHEMBL4072 P07858 Cathepsin B 90.17% 93.67%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 89.43% 91.03%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.63% 91.24%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.05% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.06% 99.23%
CHEMBL5255 O00206 Toll-like receptor 4 82.28% 92.50%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.81% 91.07%
CHEMBL1075317 P61964 WD repeat-containing protein 5 81.68% 96.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.64% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.66% 90.71%
CHEMBL325 Q13547 Histone deacetylase 1 80.55% 95.92%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.27% 94.33%

Plants that contains it

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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.
Syzygium jambos

Cross-Links

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PubChem 44575909
NPASS NPC224072