Preussin B

Details

Top
Internal ID c7cda4bf-6f2b-461a-8da3-312cbf72a183
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Amines > Aralkylamines
IUPAC Name (2S,3S,5R)-2-benzyl-5-heptyl-1-methylpyrrolidin-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H31NO/c1-3-4-5-6-10-13-17-15-19(21)18(20(17)2)14-16-11-8-7-9-12-16/h7-9,11-12,17-19,21H,3-6,10,13-15H2,1-2H3/t17-,18+,19+/m1/s1
InChI Key WVQIMRKACPTMIH-QYZOEREBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H31NO
Molecular Weight 289.50 g/mol
Exact Mass 289.240564612 g/mol
Topological Polar Surface Area (TPSA) 23.50 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.02
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

Top
(2S,3S,5R)-2-benzyl-5-heptyl-1-methylpyrrolidin-3-ol
RefChem:175967
Preubetain B
CHEBI:206240

2D Structure

Top
2D Structure of Preussin B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9878 98.78%
Caco-2 + 0.8635 86.35%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.4635 46.35%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9167 91.67%
OATP1B3 inhibitior + 0.9377 93.77%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior + 0.7743 77.43%
P-glycoprotein inhibitior - 0.8636 86.36%
P-glycoprotein substrate + 0.5087 50.87%
CYP3A4 substrate + 0.5084 50.84%
CYP2C9 substrate - 0.8132 81.32%
CYP2D6 substrate + 0.7367 73.67%
CYP3A4 inhibition - 0.8749 87.49%
CYP2C9 inhibition - 0.8763 87.63%
CYP2C19 inhibition - 0.7645 76.45%
CYP2D6 inhibition - 0.5626 56.26%
CYP1A2 inhibition - 0.7093 70.93%
CYP2C8 inhibition - 0.7556 75.56%
CYP inhibitory promiscuity - 0.8103 81.03%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6875 68.75%
Eye corrosion - 0.9748 97.48%
Eye irritation - 0.9909 99.09%
Skin irritation - 0.6914 69.14%
Skin corrosion - 0.7095 70.95%
Ames mutagenesis - 0.8354 83.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8518 85.18%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.5427 54.27%
skin sensitisation - 0.8268 82.68%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8950 89.50%
Acute Oral Toxicity (c) III 0.6403 64.03%
Estrogen receptor binding + 0.6732 67.32%
Androgen receptor binding - 0.6010 60.10%
Thyroid receptor binding - 0.5879 58.79%
Glucocorticoid receptor binding - 0.6970 69.70%
Aromatase binding - 0.7610 76.10%
PPAR gamma - 0.6082 60.82%
Honey bee toxicity - 0.9758 97.58%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7011 70.11%
Fish aquatic toxicity - 0.3682 36.82%

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
CHEMBL2581 P07339 Cathepsin D 99.16% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.98% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 97.13% 90.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.41% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.96% 85.94%
CHEMBL240 Q12809 HERG 93.30% 89.76%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.00% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.95% 95.56%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 86.81% 97.64%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.82% 99.17%
CHEMBL3891 P07384 Calpain 1 85.81% 93.04%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.67% 86.33%
CHEMBL230 P35354 Cyclooxygenase-2 84.33% 89.63%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 83.98% 90.24%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.76% 92.86%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.05% 93.56%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.06% 96.25%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.82% 94.62%

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 102367581
LOTUS LTS0047514
wikiData Q105313673