Patellin 6

Details

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Internal ID 83a46a98-5661-495b-9631-cbf283790bad
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name (2S,5S,8S,14S,17S,23S,26S,29R)-23-benzyl-5,26-bis[(1R)-1-(2-methylbut-3-en-2-yloxy)ethyl]-2,14-di(propan-2-yl)-31-thia-3,6,12,15,21,24,27,32-octazatetracyclo[27.2.1.08,12.017,21]dotriacont-1(32)-ene-4,7,13,16,22,25,28-heptone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C50H74N8O9S/c1-13-49(9,10)66-30(7)39-44(62)51-33(26-32-20-16-15-17-21-32)47(64)57-24-18-22-35(57)42(60)54-38(29(5)6)48(65)58-25-19-23-36(58)43(61)56-40(31(8)67-50(11,12)14-2)45(63)53-37(28(3)4)46-52-34(27-68-46)41(59)55-39/h13-17,20-21,28-31,33-40H,1-2,18-19,22-27H2,3-12H3,(H,51,62)(H,53,63)(H,54,60)(H,55,59)(H,56,61)/t30-,31-,33+,34+,35+,36+,37+,38+,39+,40+/m1/s1
InChI Key YDNNIZIPQWRRKH-OUJDMZAPSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C50H74N8O9S
Molecular Weight 963.20 g/mol
Exact Mass 962.52994714 g/mol
Topological Polar Surface Area (TPSA) 242.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 12

Synonyms

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SCHEMBL3503129

2D Structure

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2D Structure of Patellin 6

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6655 66.55%
Caco-2 - 0.8574 85.74%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6443 64.43%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.8630 86.30%
OATP1B3 inhibitior + 0.9345 93.45%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9806 98.06%
P-glycoprotein inhibitior + 0.7557 75.57%
P-glycoprotein substrate + 0.7229 72.29%
CYP3A4 substrate + 0.6934 69.34%
CYP2C9 substrate - 0.6095 60.95%
CYP2D6 substrate - 0.8211 82.11%
CYP3A4 inhibition + 0.6633 66.33%
CYP2C9 inhibition - 0.7850 78.50%
CYP2C19 inhibition - 0.6515 65.15%
CYP2D6 inhibition - 0.8702 87.02%
CYP1A2 inhibition - 0.8202 82.02%
CYP2C8 inhibition + 0.6072 60.72%
CYP inhibitory promiscuity - 0.8463 84.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5926 59.26%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.9032 90.32%
Skin irritation - 0.7559 75.59%
Skin corrosion - 0.9150 91.50%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6456 64.56%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.5014 50.14%
skin sensitisation - 0.8230 82.30%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.7531 75.31%
Acute Oral Toxicity (c) III 0.6030 60.30%
Estrogen receptor binding + 0.7970 79.70%
Androgen receptor binding + 0.7301 73.01%
Thyroid receptor binding + 0.6257 62.57%
Glucocorticoid receptor binding + 0.6763 67.63%
Aromatase binding + 0.6070 60.70%
PPAR gamma + 0.7984 79.84%
Honey bee toxicity - 0.7493 74.93%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9780 97.80%

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 99.64% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.97% 94.45%
CHEMBL3524 P56524 Histone deacetylase 4 96.97% 92.97%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 96.53% 97.64%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.47% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.02% 95.56%
CHEMBL1902 P62942 FK506-binding protein 1A 95.36% 97.05%
CHEMBL5103 Q969S8 Histone deacetylase 10 94.58% 90.08%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.98% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.62% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 92.03% 82.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.98% 97.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.60% 94.62%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 90.19% 93.00%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 89.66% 94.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.31% 86.33%
CHEMBL5203 P33316 dUTP pyrophosphatase 87.72% 99.18%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.31% 97.25%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.88% 93.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.80% 91.11%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.05% 97.14%
CHEMBL284 P27487 Dipeptidyl peptidase IV 82.24% 95.69%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.34% 95.89%
CHEMBL4447 Q9Y337 Kallikrein 5 80.71% 87.50%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 80.29% 91.43%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10350938
LOTUS LTS0213512
wikiData Q105346848