CID 10772032

Details

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Internal ID 50535d84-0df2-4ab4-ab61-8b9a7f078373
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Eicosanoids > Prostaglandins and related compounds
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C54H76N2O9/c1-27-43-39(63-53(27)17-15-46(5,59)26-62-53)24-51(49(43,8)60)31-12-10-29-18-35-37(22-47(29,6)33(31)20-41(51)57)55-36-19-30-11-13-32-34(48(30,7)23-38(36)56-35)21-42(58)52(32)25-40-44(50(52,9)61)28(2)54(64-40)16-14-45(3,4)65-54/h27-34,39-40,43-44,59-61H,10-26H2,1-9H3/t27-,28-,29-,30-,31+,32+,33-,34-,39-,40-,43-,44-,46-,47-,48-,49-,50-,51-,52-,53+,54+/m0/s1
InChI Key BPTQMCCKFFEOTA-WOJMQZLXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C54H76N2O9
Molecular Weight 897.20 g/mol
Exact Mass 896.55508201 g/mol
Topological Polar Surface Area (TPSA) 158.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 7.04
H-Bond Acceptor 11
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 10772032

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9813 98.13%
Caco-2 - 0.8527 85.27%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5438 54.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8667 86.67%
OATP1B3 inhibitior + 0.8911 89.11%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5614 56.14%
BSEP inhibitior + 0.9536 95.36%
P-glycoprotein inhibitior + 0.7548 75.48%
P-glycoprotein substrate + 0.5964 59.64%
CYP3A4 substrate + 0.7257 72.57%
CYP2C9 substrate - 0.7925 79.25%
CYP2D6 substrate - 0.8128 81.28%
CYP3A4 inhibition - 0.8766 87.66%
CYP2C9 inhibition - 0.9061 90.61%
CYP2C19 inhibition - 0.8924 89.24%
CYP2D6 inhibition - 0.9222 92.22%
CYP1A2 inhibition - 0.7091 70.91%
CYP2C8 inhibition + 0.5919 59.19%
CYP inhibitory promiscuity - 0.9495 94.95%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6102 61.02%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9021 90.21%
Skin irritation - 0.7712 77.12%
Skin corrosion - 0.9354 93.54%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3800 38.00%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8582 85.82%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.7857 78.57%
Acute Oral Toxicity (c) III 0.6217 62.17%
Estrogen receptor binding + 0.7927 79.27%
Androgen receptor binding + 0.7770 77.70%
Thyroid receptor binding + 0.5683 56.83%
Glucocorticoid receptor binding + 0.7591 75.91%
Aromatase binding + 0.6533 65.33%
PPAR gamma + 0.7915 79.15%
Honey bee toxicity - 0.7639 76.39%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.8681 86.81%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.93% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.17% 99.23%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 93.65% 98.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.75% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.08% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.19% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.18% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.60% 94.45%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 87.71% 96.38%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.05% 94.00%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 84.70% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.92% 93.04%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.85% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 83.67% 94.75%
CHEMBL2581 P07339 Cathepsin D 82.73% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.16% 95.56%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 82.13% 96.39%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 81.84% 98.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.72% 95.89%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 81.62% 98.46%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.26% 92.62%

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 10772032
LOTUS LTS0051461
wikiData Q104943930