Isaridin B

Details

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Internal ID f8df5963-39b9-4fcb-bb2c-e4aaa2ef0f00
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name (3S,10S,13S,16S,19S,20S)-10,16-dibenzyl-11,14,20-trimethyl-3-(2-methylpropyl)-13-propan-2-yl-4-oxa-1,8,11,14,17-pentazabicyclo[17.3.0]docosane-2,5,9,12,15,18-hexone
SMILES (Canonical) CC1CCN2C1C(=O)NC(C(=O)N(C(C(=O)N(C(C(=O)NCCC(=O)OC(C2=O)CC(C)C)CC3=CC=CC=C3)C)C(C)C)C)CC4=CC=CC=C4
SMILES (Isomeric) C[C@H]1CCN2[C@@H]1C(=O)N[C@H](C(=O)N([C@H](C(=O)N([C@H](C(=O)NCCC(=O)O[C@H](C2=O)CC(C)C)CC3=CC=CC=C3)C)C(C)C)C)CC4=CC=CC=C4
InChI InChI=1S/C40H55N5O7/c1-25(2)22-32-39(50)45-21-19-27(5)35(45)37(48)42-30(23-28-14-10-8-11-15-28)38(49)44(7)34(26(3)4)40(51)43(6)31(24-29-16-12-9-13-17-29)36(47)41-20-18-33(46)52-32/h8-17,25-27,30-32,34-35H,18-24H2,1-7H3,(H,41,47)(H,42,48)/t27-,30-,31-,32-,34-,35-/m0/s1
InChI Key CYKMKVMZXCFAKS-GPUGIWAMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C40H55N5O7
Molecular Weight 717.90 g/mol
Exact Mass 717.41014911 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP 5.10
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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CHEMBL3286772

2D Structure

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2D Structure of Isaridin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6911 69.11%
Caco-2 - 0.8019 80.19%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Lysosomes 0.6806 68.06%
OATP2B1 inhibitior + 0.5749 57.49%
OATP1B1 inhibitior + 0.8414 84.14%
OATP1B3 inhibitior + 0.9194 91.94%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9628 96.28%
P-glycoprotein inhibitior + 0.8352 83.52%
P-glycoprotein substrate + 0.8329 83.29%
CYP3A4 substrate + 0.6884 68.84%
CYP2C9 substrate - 0.5779 57.79%
CYP2D6 substrate - 0.8150 81.50%
CYP3A4 inhibition - 0.8196 81.96%
CYP2C9 inhibition - 0.6686 66.86%
CYP2C19 inhibition - 0.6133 61.33%
CYP2D6 inhibition - 0.8989 89.89%
CYP1A2 inhibition - 0.9486 94.86%
CYP2C8 inhibition + 0.5091 50.91%
CYP inhibitory promiscuity - 0.8769 87.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5991 59.91%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9351 93.51%
Skin irritation - 0.7954 79.54%
Skin corrosion - 0.9323 93.23%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7428 74.28%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.6427 64.27%
skin sensitisation - 0.9018 90.18%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.8767 87.67%
Acute Oral Toxicity (c) III 0.6461 64.61%
Estrogen receptor binding + 0.7704 77.04%
Androgen receptor binding + 0.6741 67.41%
Thyroid receptor binding + 0.5884 58.84%
Glucocorticoid receptor binding + 0.7264 72.64%
Aromatase binding + 0.5761 57.61%
PPAR gamma + 0.7916 79.16%
Honey bee toxicity - 0.7899 78.99%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8208 82.08%

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 99.77% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.42% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.93% 95.56%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 92.62% 97.64%
CHEMBL226 P30542 Adenosine A1 receptor 91.55% 95.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.45% 97.25%
CHEMBL333 P08253 Matrix metalloproteinase-2 88.29% 96.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.42% 91.11%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.64% 93.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.54% 86.33%
CHEMBL255 P29275 Adenosine A2b receptor 86.38% 98.59%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.24% 95.89%
CHEMBL1949 P62937 Cyclophilin A 83.85% 98.57%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 83.47% 95.71%
CHEMBL4072 P07858 Cathepsin B 83.15% 93.67%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.12% 90.08%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.97% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.58% 99.23%
CHEMBL4588 P22894 Matrix metalloproteinase 8 82.25% 94.66%
CHEMBL4616 Q92847 Ghrelin receptor 82.14% 92.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.81% 96.25%
CHEMBL2189110 Q15910 Histone-lysine N-methyltransferase EZH2 81.41% 97.50%
CHEMBL228 P31645 Serotonin transporter 80.32% 95.51%

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 90680632
LOTUS LTS0039099
wikiData Q77280847