6,8,23-Trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-17,20-diol

Details

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Internal ID 7b61591a-2c5b-42e2-b713-ff02073ad290
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal alkaloids > Cerveratrum-type alkaloids
IUPAC Name 6,8,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-17,20-diol
SMILES (Canonical) CC1CC(C2CC3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C
SMILES (Isomeric) CC1CC(C2CC3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C
InChI InChI=1S/C27H45NO2/c1-15-8-16(2)25-9-17-4-5-19-20(22(17)14-28(25)13-15)11-23-21(19)12-26(30)24-10-18(29)6-7-27(23,24)3/h15-26,29-30H,4-14H2,1-3H3
InChI Key YIYKJKFLANHXRV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H45NO2
Molecular Weight 415.70 g/mol
Exact Mass 415.345029678 g/mol
Topological Polar Surface Area (TPSA) 43.70 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.56
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6,8,23-Trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-17,20-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9803 98.03%
Caco-2 - 0.6185 61.85%
Blood Brain Barrier + 0.8379 83.79%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.7018 70.18%
OATP2B1 inhibitior - 0.5848 58.48%
OATP1B1 inhibitior + 0.9222 92.22%
OATP1B3 inhibitior + 0.9454 94.54%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8197 81.97%
P-glycoprotein inhibitior - 0.8022 80.22%
P-glycoprotein substrate + 0.5410 54.10%
CYP3A4 substrate + 0.7198 71.98%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate + 0.5867 58.67%
CYP3A4 inhibition - 0.7994 79.94%
CYP2C9 inhibition - 0.8872 88.72%
CYP2C19 inhibition - 0.9076 90.76%
CYP2D6 inhibition + 0.5682 56.82%
CYP1A2 inhibition - 0.8887 88.87%
CYP2C8 inhibition - 0.7616 76.16%
CYP inhibitory promiscuity - 0.9866 98.66%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5909 59.09%
Eye corrosion - 0.9817 98.17%
Eye irritation - 0.8698 86.98%
Skin irritation - 0.7034 70.34%
Skin corrosion - 0.7794 77.94%
Ames mutagenesis - 0.6715 67.15%
Human Ether-a-go-go-Related Gene inhibition - 0.6191 61.91%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.5839 58.39%
skin sensitisation - 0.8286 82.86%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.6869 68.69%
Acute Oral Toxicity (c) III 0.6281 62.81%
Estrogen receptor binding + 0.6123 61.23%
Androgen receptor binding + 0.7507 75.07%
Thyroid receptor binding + 0.5838 58.38%
Glucocorticoid receptor binding + 0.6527 65.27%
Aromatase binding + 0.5481 54.81%
PPAR gamma + 0.5321 53.21%
Honey bee toxicity - 0.7474 74.74%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.8205 82.05%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.50% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.09% 97.25%
CHEMBL238 Q01959 Dopamine transporter 95.59% 95.88%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 94.80% 82.69%
CHEMBL218 P21554 Cannabinoid CB1 receptor 94.30% 96.61%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 91.89% 94.78%
CHEMBL325 Q13547 Histone deacetylase 1 91.30% 95.92%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 91.17% 95.58%
CHEMBL1871 P10275 Androgen Receptor 88.07% 96.43%
CHEMBL233 P35372 Mu opioid receptor 88.07% 97.93%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.74% 92.86%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.60% 97.09%
CHEMBL284 P27487 Dipeptidyl peptidase IV 86.43% 95.69%
CHEMBL226 P30542 Adenosine A1 receptor 86.03% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.57% 100.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.25% 91.03%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 84.82% 89.05%
CHEMBL237 P41145 Kappa opioid receptor 83.93% 98.10%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 82.07% 98.46%
CHEMBL4506 Q96EB6 NAD-dependent deacetylase sirtuin 1 82.03% 88.33%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 81.81% 95.52%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 81.64% 97.33%
CHEMBL259 P32245 Melanocortin receptor 4 80.93% 95.38%
CHEMBL204 P00734 Thrombin 80.63% 96.01%

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.
Fritillaria imperialis

Cross-Links

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PubChem 4600130
LOTUS LTS0120177
wikiData Q105349123