(1R,8S,10R,15S,22S,23R,29R,32R)-23,32-dimethyl-9,30-dioxa-11,25-diazapentacyclo[20.6.2.28,11.010,15.025,29]dotriacontane

Details

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Internal ID 49391114-b0f4-4793-aa21-25f71c6f3a7d
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name (1R,8S,10R,15S,22S,23R,29R,32R)-23,32-dimethyl-9,30-dioxa-11,25-diazapentacyclo[20.6.2.28,11.010,15.025,29]dotriacontane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H54N2O2/c1-23-21-31-19-11-15-25-13-8-4-6-10-18-28-24(2)22-32-20-12-16-26(30(32)34-28)14-7-3-5-9-17-27(23)33-29(25)31/h23-30H,3-22H2,1-2H3/t23-,24-,25-,26+,27+,28+,29-,30-/m1/s1
InChI Key RWXBZLYIOQLHHZ-QJDBZLDESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H54N2O2
Molecular Weight 474.80 g/mol
Exact Mass 474.41852897 g/mol
Topological Polar Surface Area (TPSA) 24.90 Ų
XlogP 8.30
Atomic LogP (AlogP) 6.83
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,8S,10R,15S,22S,23R,29R,32R)-23,32-dimethyl-9,30-dioxa-11,25-diazapentacyclo[20.6.2.28,11.010,15.025,29]dotriacontane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9798 97.98%
Caco-2 + 0.5551 55.51%
Blood Brain Barrier + 0.9129 91.29%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.3747 37.47%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9497 94.97%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.6873 68.73%
P-glycoprotein inhibitior - 0.6055 60.55%
P-glycoprotein substrate - 0.8833 88.33%
CYP3A4 substrate - 0.5255 52.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7128 71.28%
CYP3A4 inhibition - 0.9295 92.95%
CYP2C9 inhibition - 0.9132 91.32%
CYP2C19 inhibition - 0.7013 70.13%
CYP2D6 inhibition - 0.9177 91.77%
CYP1A2 inhibition - 0.7503 75.03%
CYP2C8 inhibition - 0.9441 94.41%
CYP inhibitory promiscuity - 0.9457 94.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6227 62.27%
Eye corrosion - 0.9552 95.52%
Eye irritation - 0.5867 58.67%
Skin irritation - 0.7140 71.40%
Skin corrosion - 0.8140 81.40%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4597 45.97%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.7683 76.83%
skin sensitisation - 0.8530 85.30%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5180 51.80%
Acute Oral Toxicity (c) III 0.6956 69.56%
Estrogen receptor binding + 0.5328 53.28%
Androgen receptor binding + 0.5195 51.95%
Thyroid receptor binding + 0.5257 52.57%
Glucocorticoid receptor binding - 0.6163 61.63%
Aromatase binding - 0.4845 48.45%
PPAR gamma - 0.6324 63.24%
Honey bee toxicity - 0.9581 95.81%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.8408 84.08%

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
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 94.73% 94.78%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.42% 97.25%
CHEMBL3012 Q13946 Phosphodiesterase 7A 90.86% 99.29%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 87.59% 98.33%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 87.50% 95.58%
CHEMBL237 P41145 Kappa opioid receptor 86.47% 98.10%
CHEMBL2581 P07339 Cathepsin D 85.55% 98.95%
CHEMBL2094108 P49354 Protein farnesyltransferase 85.54% 97.92%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.28% 99.18%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 84.38% 98.99%
CHEMBL4777 P25929 Neuropeptide Y receptor type 1 84.28% 96.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.07% 96.09%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 83.96% 95.27%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.73% 97.09%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 83.66% 98.46%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.34% 93.04%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.32% 95.50%
CHEMBL5255 O00206 Toll-like receptor 4 83.19% 92.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.31% 92.94%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.79% 90.24%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.93% 95.89%
CHEMBL3023 Q9NRA0 Sphingosine kinase 2 80.51% 95.61%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.20% 93.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.18% 100.00%

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.
There are no matching plants.

Cross-Links

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PubChem 21575356
LOTUS LTS0257940
wikiData Q105246819