40-Tert-butyl-10,12,16,20,22,24,28,32,36-nonahydroxy-4-methyl-1-oxacyclotetracont-3-en-2-one

Details

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Internal ID e803dd7d-9383-463f-8c14-d34323a358e1
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 40-tert-butyl-10,12,16,20,22,24,28,32,36-nonahydroxy-4-methyl-1-oxacyclotetracont-3-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C44H84O11/c1-32-14-6-5-7-15-37(49)29-38(50)24-10-20-35(47)22-12-26-40(52)31-41(53)30-39(51)25-11-21-34(46)18-8-16-33(45)17-9-19-36(48)23-13-27-42(44(2,3)4)55-43(54)28-32/h28,33-42,45-53H,5-27,29-31H2,1-4H3
InChI Key GMYBARKHHWBGAC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C44H84O11
Molecular Weight 789.10 g/mol
Exact Mass 788.60136349 g/mol
Topological Polar Surface Area (TPSA) 208.00 Ų
XlogP 6.10
Atomic LogP (AlogP) 6.29
H-Bond Acceptor 11
H-Bond Donor 9
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 40-Tert-butyl-10,12,16,20,22,24,28,32,36-nonahydroxy-4-methyl-1-oxacyclotetracont-3-en-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9362 93.62%
Caco-2 - 0.8343 83.43%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6533 65.33%
OATP2B1 inhibitior - 0.5679 56.79%
OATP1B1 inhibitior + 0.8805 88.05%
OATP1B3 inhibitior + 0.8938 89.38%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.7970 79.70%
P-glycoprotein inhibitior + 0.6946 69.46%
P-glycoprotein substrate - 0.8147 81.47%
CYP3A4 substrate + 0.5587 55.87%
CYP2C9 substrate - 0.7891 78.91%
CYP2D6 substrate - 0.8988 89.88%
CYP3A4 inhibition - 0.8177 81.77%
CYP2C9 inhibition - 0.7242 72.42%
CYP2C19 inhibition - 0.6725 67.25%
CYP2D6 inhibition - 0.9487 94.87%
CYP1A2 inhibition - 0.7108 71.08%
CYP2C8 inhibition - 0.8818 88.18%
CYP inhibitory promiscuity - 0.9544 95.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9128 91.28%
Carcinogenicity (trinary) Non-required 0.6446 64.46%
Eye corrosion - 0.9765 97.65%
Eye irritation - 0.8956 89.56%
Skin irritation + 0.5100 51.00%
Skin corrosion - 0.9532 95.32%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4014 40.14%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.6979 69.79%
skin sensitisation - 0.6435 64.35%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5170 51.70%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6572 65.72%
Acute Oral Toxicity (c) III 0.4649 46.49%
Estrogen receptor binding + 0.7800 78.00%
Androgen receptor binding - 0.5858 58.58%
Thyroid receptor binding - 0.5859 58.59%
Glucocorticoid receptor binding - 0.4654 46.54%
Aromatase binding + 0.6473 64.73%
PPAR gamma + 0.6034 60.34%
Honey bee toxicity - 0.8846 88.46%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9264 92.64%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.94% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.13% 97.25%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 92.66% 93.04%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.13% 97.09%
CHEMBL2581 P07339 Cathepsin D 90.21% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 90.02% 91.49%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 86.73% 90.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.13% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.82% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.40% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.13% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.72% 93.03%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.64% 93.56%
CHEMBL1871 P10275 Androgen Receptor 82.37% 96.43%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.67% 92.94%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.90% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.62% 96.61%
CHEMBL3012 Q13946 Phosphodiesterase 7A 80.31% 99.29%
CHEMBL259 P32245 Melanocortin receptor 4 80.23% 95.38%

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 163091266
LOTUS LTS0229757
wikiData Q104167303