Pseudostellarin B

Details

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Internal ID fdb7c29c-e6a2-4d89-8854-d60817db5887
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name (3S,18S,24S,27S)-24-benzyl-18-[(2S)-butan-2-yl]-1,7,10,13,16,19,22,25-octazatricyclo[25.3.0.03,7]triacontane-2,8,11,14,17,20,23,26-octone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H46N8O8/c1-3-20(2)29-32(48)37-17-26(43)34-16-25(42)35-19-28(45)40-13-8-12-24(40)33(49)41-14-7-11-23(41)31(47)38-22(15-21-9-5-4-6-10-21)30(46)36-18-27(44)39-29/h4-6,9-10,20,22-24,29H,3,7-8,11-19H2,1-2H3,(H,34,43)(H,35,42)(H,36,46)(H,37,48)(H,38,47)(H,39,44)/t20-,22-,23-,24-,29-/m0/s1
InChI Key QFUNIUYCQLWNMO-BHUZBVAGSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C33H46N8O8
Molecular Weight 682.80 g/mol
Exact Mass 682.34386046 g/mol
Topological Polar Surface Area (TPSA) 215.00 Ų
XlogP -0.10
Atomic LogP (AlogP) -2.29
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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156430-21-6
orb2893450
SCHEMBL29779774

2D Structure

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2D Structure of Pseudostellarin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9360 93.60%
Caco-2 - 0.8669 86.69%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5018 50.18%
OATP2B1 inhibitior - 0.7099 70.99%
OATP1B1 inhibitior + 0.8737 87.37%
OATP1B3 inhibitior + 0.9402 94.02%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8716 87.16%
P-glycoprotein inhibitior + 0.7974 79.74%
P-glycoprotein substrate + 0.7975 79.75%
CYP3A4 substrate + 0.6454 64.54%
CYP2C9 substrate - 0.6180 61.80%
CYP2D6 substrate - 0.7959 79.59%
CYP3A4 inhibition - 0.9488 94.88%
CYP2C9 inhibition - 0.8671 86.71%
CYP2C19 inhibition - 0.7970 79.70%
CYP2D6 inhibition - 0.9315 93.15%
CYP1A2 inhibition - 0.9464 94.64%
CYP2C8 inhibition - 0.5694 56.94%
CYP inhibitory promiscuity - 0.9737 97.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6920 69.20%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9309 93.09%
Skin irritation - 0.7905 79.05%
Skin corrosion - 0.9317 93.17%
Ames mutagenesis - 0.6954 69.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7240 72.40%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.5372 53.72%
skin sensitisation - 0.9205 92.05%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.4561 45.61%
Acute Oral Toxicity (c) III 0.6557 65.57%
Estrogen receptor binding + 0.7513 75.13%
Androgen receptor binding + 0.7026 70.26%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6012 60.12%
Aromatase binding + 0.5789 57.89%
PPAR gamma + 0.6941 69.41%
Honey bee toxicity - 0.8094 80.94%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.6773 67.73%

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 99.78% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.83% 96.09%
CHEMBL3524 P56524 Histone deacetylase 4 96.74% 92.97%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 95.52% 97.64%
CHEMBL4071 P08311 Cathepsin G 95.05% 94.64%
CHEMBL3202 P48147 Prolyl endopeptidase 93.03% 90.65%
CHEMBL333 P08253 Matrix metalloproteinase-2 92.81% 96.31%
CHEMBL221 P23219 Cyclooxygenase-1 92.47% 90.17%
CHEMBL1902 P62942 FK506-binding protein 1A 92.36% 97.05%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.60% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 91.24% 90.08%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.20% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 91.16% 82.38%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.58% 94.45%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.37% 97.14%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.04% 93.03%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.42% 93.00%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 86.23% 92.67%
CHEMBL4616 Q92847 Ghrelin receptor 85.89% 92.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.77% 99.18%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.79% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.67% 86.33%
CHEMBL228 P31645 Serotonin transporter 84.66% 95.51%
CHEMBL4447 Q9Y337 Kallikrein 5 84.15% 87.50%
CHEMBL2443 P49862 Kallikrein 7 83.99% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.41% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.00% 97.25%
CHEMBL255 P29275 Adenosine A2b receptor 81.27% 98.59%

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.
Pseudostellaria heterophylla

Cross-Links

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PubChem 10078303
NPASS NPC89561
LOTUS LTS0022998
wikiData Q105219769