36-Hexan-2-yl-8,10,14,18,22,26,28,30,34-nonahydroxy-4-methyl-1-oxacyclohexatriacont-3-en-2-one

Details

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Internal ID 8a3126fd-1056-47a8-8654-07b53c7e18c1
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 36-hexan-2-yl-8,10,14,18,22,26,28,30,34-nonahydroxy-4-methyl-1-oxacyclohexatriacont-3-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H80O11/c1-4-5-13-31(3)41-29-39(50)24-11-23-38(49)28-40(51)27-37(48)22-10-19-34(45)17-8-15-32(43)14-7-16-33(44)18-9-21-36(47)26-35(46)20-6-12-30(2)25-42(52)53-41/h25,31-41,43-51H,4-24,26-29H2,1-3H3
InChI Key XCMPEWXFVPCAPO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C42H80O11
Molecular Weight 761.10 g/mol
Exact Mass 760.57006336 g/mol
Topological Polar Surface Area (TPSA) 208.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.51
H-Bond Acceptor 11
H-Bond Donor 9
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 36-Hexan-2-yl-8,10,14,18,22,26,28,30,34-nonahydroxy-4-methyl-1-oxacyclohexatriacont-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 + 0.9399 93.99%
Caco-2 - 0.8482 84.82%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6059 60.59%
OATP2B1 inhibitior - 0.5679 56.79%
OATP1B1 inhibitior + 0.8439 84.39%
OATP1B3 inhibitior + 0.9473 94.73%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior + 0.6245 62.45%
P-glycoprotein substrate - 0.5605 56.05%
CYP3A4 substrate + 0.5836 58.36%
CYP2C9 substrate - 0.5839 58.39%
CYP2D6 substrate - 0.8992 89.92%
CYP3A4 inhibition + 0.7174 71.74%
CYP2C9 inhibition - 0.8727 87.27%
CYP2C19 inhibition + 0.6778 67.78%
CYP2D6 inhibition - 0.9152 91.52%
CYP1A2 inhibition - 0.8319 83.19%
CYP2C8 inhibition - 0.8914 89.14%
CYP inhibitory promiscuity - 0.8600 86.00%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6875 68.75%
Eye corrosion - 0.9787 97.87%
Eye irritation - 0.8981 89.81%
Skin irritation - 0.6159 61.59%
Skin corrosion - 0.9449 94.49%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4777 47.77%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5940 59.40%
skin sensitisation - 0.7724 77.24%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.4660 46.60%
Acute Oral Toxicity (c) III 0.5165 51.65%
Estrogen receptor binding + 0.7323 73.23%
Androgen receptor binding - 0.5185 51.85%
Thyroid receptor binding - 0.6084 60.84%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.5490 54.90%
PPAR gamma + 0.5579 55.79%
Honey bee toxicity - 0.9473 94.73%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9436 94.36%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.80% 97.25%
CHEMBL2581 P07339 Cathepsin D 96.52% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.43% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.52% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 91.42% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.23% 93.56%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 88.09% 95.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.48% 96.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.45% 96.47%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.83% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.45% 100.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.23% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.15% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.99% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 85.48% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.04% 99.17%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.99% 90.08%
CHEMBL1871 P10275 Androgen Receptor 81.40% 96.43%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.12% 98.33%

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 75244394
LOTUS LTS0197135
wikiData Q104200844