(7S)-27-cyclohexylheptacosan-7-ol

Details

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Internal ID 5c20ab5f-a163-48f1-8f39-b66450690e9f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (7S)-27-cyclohexylheptacosan-7-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H66O/c1-2-3-4-25-30-33(34)31-26-20-18-16-14-12-10-8-6-5-7-9-11-13-15-17-19-22-27-32-28-23-21-24-29-32/h32-34H,2-31H2,1H3/t33-/m0/s1
InChI Key NIPOHIIZDFDXPX-XIFFEERXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C33H66O
Molecular Weight 478.90 g/mol
Exact Mass 478.511366725 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 15.70
Atomic LogP (AlogP) 11.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 26

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (7S)-27-cyclohexylheptacosan-7-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 - 0.6702 67.02%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.4526 45.26%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9551 95.51%
OATP1B3 inhibitior + 0.9088 90.88%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5328 53.28%
P-glycoprotein inhibitior - 0.7440 74.40%
P-glycoprotein substrate - 0.6998 69.98%
CYP3A4 substrate - 0.5608 56.08%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.6696 66.96%
CYP3A4 inhibition - 0.9248 92.48%
CYP2C9 inhibition - 0.8786 87.86%
CYP2C19 inhibition - 0.8959 89.59%
CYP2D6 inhibition - 0.9094 90.94%
CYP1A2 inhibition + 0.5562 55.62%
CYP2C8 inhibition - 0.8156 81.56%
CYP inhibitory promiscuity - 0.8210 82.10%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.6868 68.68%
Eye corrosion + 0.7766 77.66%
Eye irritation - 0.4802 48.02%
Skin irritation + 0.7956 79.56%
Skin corrosion - 0.6432 64.32%
Ames mutagenesis - 0.8837 88.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5903 59.03%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6208 62.08%
skin sensitisation + 0.9278 92.78%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6759 67.59%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.7520 75.20%
Acute Oral Toxicity (c) III 0.7247 72.47%
Estrogen receptor binding - 0.4796 47.96%
Androgen receptor binding - 0.8034 80.34%
Thyroid receptor binding + 0.5898 58.98%
Glucocorticoid receptor binding - 0.4709 47.09%
Aromatase binding - 0.5996 59.96%
PPAR gamma - 0.5151 51.51%
Honey bee toxicity - 0.9885 98.85%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5980 59.80%
Fish aquatic toxicity + 0.8728 87.28%

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 98.60% 97.25%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 98.05% 90.24%
CHEMBL2581 P07339 Cathepsin D 97.52% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.90% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 95.65% 93.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 94.88% 100.00%
CHEMBL230 P35354 Cyclooxygenase-2 94.64% 89.63%
CHEMBL1968 P07099 Epoxide hydrolase 1 93.75% 98.57%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 93.26% 91.81%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 93.02% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.71% 92.86%
CHEMBL240 Q12809 HERG 91.16% 89.76%
CHEMBL1914 P06276 Butyrylcholinesterase 90.61% 95.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.59% 97.09%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 90.51% 95.50%
CHEMBL2996 Q05655 Protein kinase C delta 89.81% 97.79%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.71% 85.94%
CHEMBL237 P41145 Kappa opioid receptor 89.67% 98.10%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.87% 95.17%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 88.11% 98.33%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 87.56% 92.88%
CHEMBL218 P21554 Cannabinoid CB1 receptor 86.94% 96.61%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.08% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.04% 92.62%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 85.95% 97.23%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 85.05% 96.00%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 84.91% 95.00%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 84.73% 95.27%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.32% 93.04%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.12% 99.17%
CHEMBL5255 O00206 Toll-like receptor 4 81.89% 92.50%
CHEMBL238 Q01959 Dopamine transporter 81.71% 95.88%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.01% 96.47%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.27% 95.89%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.22% 99.18%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Achyranthes aspera

Cross-Links

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PubChem 162905743
LOTUS LTS0038734
wikiData Q105179942