Cyclipostin H

Details

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Internal ID e21d5c49-c569-429a-86b5-dff8c5d54e21
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3R,8aR)-5-methyl-3-oxo-3-(12-oxohexadecoxy)-8,8a-dihydro-1H-furo[3,4-e][1,3,2]dioxaphosphepin-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H39O7P/c1-3-4-14-21(24)15-12-10-8-6-5-7-9-11-13-16-28-31(26)29-18-20-17-27-23(25)22(20)19(2)30-31/h20H,3-18H2,1-2H3/t20-,31-/m1/s1
InChI Key OPNLFNJWZHCEQY-PLTNMMHCSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C23H39O7P
Molecular Weight 458.50 g/mol
Exact Mass 458.24334058 g/mol
Topological Polar Surface Area (TPSA) 88.10 Ų
XlogP 5.10
Atomic LogP (AlogP) 6.27
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cyclipostin H

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9819 98.19%
Caco-2 - 0.5779 57.79%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6107 61.07%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7388 73.88%
P-glycoprotein inhibitior + 0.5901 59.01%
P-glycoprotein substrate - 0.6265 62.65%
CYP3A4 substrate + 0.6133 61.33%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8850 88.50%
CYP3A4 inhibition - 0.7191 71.91%
CYP2C9 inhibition - 0.7722 77.22%
CYP2C19 inhibition - 0.7313 73.13%
CYP2D6 inhibition - 0.8765 87.65%
CYP1A2 inhibition - 0.6956 69.56%
CYP2C8 inhibition - 0.6193 61.93%
CYP inhibitory promiscuity - 0.8576 85.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5212 52.12%
Eye corrosion - 0.9493 94.93%
Eye irritation - 0.6624 66.24%
Skin irritation - 0.7243 72.43%
Skin corrosion - 0.9130 91.30%
Ames mutagenesis - 0.7454 74.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3761 37.61%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.5413 54.13%
skin sensitisation - 0.8578 85.78%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6468 64.68%
Acute Oral Toxicity (c) III 0.4299 42.99%
Estrogen receptor binding + 0.5631 56.31%
Androgen receptor binding + 0.7090 70.90%
Thyroid receptor binding - 0.5668 56.68%
Glucocorticoid receptor binding + 0.5585 55.85%
Aromatase binding + 0.5681 56.81%
PPAR gamma + 0.5450 54.50%
Honey bee toxicity - 0.9014 90.14%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6224 62.24%
Fish aquatic toxicity + 0.9936 99.36%

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 96.74% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.08% 99.17%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 94.79% 85.94%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.67% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.44% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.13% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.41% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 87.75% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.75% 95.56%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.45% 91.24%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.92% 96.95%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.85% 90.08%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.83% 92.08%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.48% 82.69%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.24% 93.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.09% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.57% 93.56%
CHEMBL5255 O00206 Toll-like receptor 4 80.52% 92.50%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.19% 97.21%

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 10895774
LOTUS LTS0148003
wikiData Q77484744