Pteratide IV

Details

Top
Internal ID 0b9b042c-f20e-480b-b35f-d177d2a78b76
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name N-[(2S)-1-[[(2S,3S)-1-[[(3S,6S,9S,12S,15S,18S,19R)-15-benzyl-6,7,9,10,16,19-hexamethyl-2,5,8,11,14,17-hexaoxo-3,12-di(propan-2-yl)-1-oxa-4,7,10,13,16-pentazacyclononadec-18-yl]amino]-3-methyl-1-oxopentan-2-yl]-methylamino]-3-methyl-1-oxobutan-2-yl]-N-methylbenzamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C52H78N8O10/c1-17-32(8)43(60(16)51(68)42(31(6)7)59(15)48(65)37-26-22-19-23-27-37)46(63)55-41-35(11)70-52(69)40(30(4)5)54-44(61)33(9)56(12)47(64)34(10)57(13)49(66)39(29(2)3)53-45(62)38(58(14)50(41)67)28-36-24-20-18-21-25-36/h18-27,29-35,38-43H,17,28H2,1-16H3,(H,53,62)(H,54,61)(H,55,63)/t32-,33-,34-,35+,38-,39-,40-,41-,42-,43-/m0/s1
InChI Key OJPMNLJZJIAKSU-FNOQMQAJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C52H78N8O10
Molecular Weight 975.20 g/mol
Exact Mass 974.58409071 g/mol
Topological Polar Surface Area (TPSA) 215.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 3.13
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 13

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Pteratide IV

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7461 74.61%
Caco-2 - 0.8553 85.53%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.3841 38.41%
OATP2B1 inhibitior + 0.5690 56.90%
OATP1B1 inhibitior + 0.8046 80.46%
OATP1B3 inhibitior + 0.9145 91.45%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9068 90.68%
BSEP inhibitior + 0.9056 90.56%
P-glycoprotein inhibitior + 0.7655 76.55%
P-glycoprotein substrate + 0.8490 84.90%
CYP3A4 substrate + 0.6947 69.47%
CYP2C9 substrate + 0.5918 59.18%
CYP2D6 substrate - 0.8587 85.87%
CYP3A4 inhibition + 0.7709 77.09%
CYP2C9 inhibition - 0.7947 79.47%
CYP2C19 inhibition - 0.6550 65.50%
CYP2D6 inhibition - 0.8620 86.20%
CYP1A2 inhibition - 0.8987 89.87%
CYP2C8 inhibition + 0.6095 60.95%
CYP inhibitory promiscuity - 0.6722 67.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.6017 60.17%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9040 90.40%
Skin irritation - 0.7961 79.61%
Skin corrosion - 0.9379 93.79%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7165 71.65%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.9013 90.13%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.7976 79.76%
Acute Oral Toxicity (c) III 0.6746 67.46%
Estrogen receptor binding + 0.7823 78.23%
Androgen receptor binding + 0.7119 71.19%
Thyroid receptor binding + 0.6028 60.28%
Glucocorticoid receptor binding + 0.7351 73.51%
Aromatase binding + 0.5837 58.37%
PPAR gamma + 0.7652 76.52%
Honey bee toxicity - 0.7793 77.93%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9679 96.79%

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 99.59% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.37% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 97.10% 90.17%
CHEMBL4072 P07858 Cathepsin B 97.06% 93.67%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.21% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.19% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 93.13% 90.08%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 92.26% 96.47%
CHEMBL3837 P07711 Cathepsin L 91.57% 96.61%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 89.37% 89.67%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 88.64% 93.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.55% 99.17%
CHEMBL1949 P62937 Cyclophilin A 86.92% 98.57%
CHEMBL4208 P20618 Proteasome component C5 86.18% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.13% 99.23%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 84.18% 96.37%
CHEMBL3401 O75469 Pregnane X receptor 83.43% 94.73%
CHEMBL2096618 P11274 Bcr/Abl fusion protein 82.44% 85.83%
CHEMBL5028 O14672 ADAM10 81.34% 97.50%

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 11974963
LOTUS LTS0120858
wikiData Q77500874