(1R,7R,10R,11S,14R,15S,18R,22R,23S)-11-methyl-5-oxa-13-azaheptacyclo[11.9.1.01,7.07,15.010,23.014,18.018,22]tricosan-4-one

Details

Top
Internal ID ac5367f5-3254-424f-972b-d01fb0f62748
Taxonomy Alkaloids and derivatives > Daphniphylline-type alkaloids
IUPAC Name (1R,7R,10R,11S,14R,15S,18R,22R,23S)-11-methyl-5-oxa-13-azaheptacyclo[11.9.1.01,7.07,15.010,23.014,18.018,22]tricosan-4-one
SMILES (Canonical) CC1CN2C3C1CCC45C3(CCC(=O)OC4)C6CCCC67C2C5CC7
SMILES (Isomeric) C[C@@H]1CN2[C@H]3[C@@H]1CC[C@@]45[C@@]3(CCC(=O)OC4)[C@@H]6CCC[C@]67[C@H]2[C@H]5CC7
InChI InChI=1S/C22H31NO2/c1-13-11-23-18-14(13)4-9-21-12-25-17(24)6-10-22(18,21)16-3-2-7-20(16)8-5-15(21)19(20)23/h13-16,18-19H,2-12H2,1H3/t13-,14-,15-,16-,18+,19-,20-,21-,22+/m1/s1
InChI Key SJPVIZHSTQMCEQ-FPTNXDLASA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C22H31NO2
Molecular Weight 341.50 g/mol
Exact Mass 341.235479232 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.62
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (1R,7R,10R,11S,14R,15S,18R,22R,23S)-11-methyl-5-oxa-13-azaheptacyclo[11.9.1.01,7.07,15.010,23.014,18.018,22]tricosan-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 + 0.7618 76.18%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.5868 58.68%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8953 89.53%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.6869 68.69%
P-glycoprotein inhibitior - 0.8452 84.52%
P-glycoprotein substrate - 0.6955 69.55%
CYP3A4 substrate + 0.6473 64.73%
CYP2C9 substrate - 0.8080 80.80%
CYP2D6 substrate - 0.6782 67.82%
CYP3A4 inhibition - 0.8778 87.78%
CYP2C9 inhibition - 0.9131 91.31%
CYP2C19 inhibition - 0.7357 73.57%
CYP2D6 inhibition - 0.8419 84.19%
CYP1A2 inhibition - 0.8151 81.51%
CYP2C8 inhibition - 0.7444 74.44%
CYP inhibitory promiscuity - 0.9486 94.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5660 56.60%
Eye corrosion - 0.9698 96.98%
Eye irritation - 0.7854 78.54%
Skin irritation - 0.7725 77.25%
Skin corrosion - 0.8729 87.29%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4126 41.26%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.6050 60.50%
skin sensitisation - 0.8141 81.41%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.5725 57.25%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.5636 56.36%
Acute Oral Toxicity (c) III 0.6395 63.95%
Estrogen receptor binding + 0.7448 74.48%
Androgen receptor binding + 0.7354 73.54%
Thyroid receptor binding + 0.5914 59.14%
Glucocorticoid receptor binding + 0.8051 80.51%
Aromatase binding + 0.7870 78.70%
PPAR gamma + 0.5507 55.07%
Honey bee toxicity - 0.8053 80.53%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.7371 73.71%

Targets

Top

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 95.15% 97.25%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 92.46% 96.38%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 92.45% 94.78%
CHEMBL2581 P07339 Cathepsin D 92.18% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.77% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.40% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.92% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.12% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.89% 96.77%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.26% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.24% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.04% 90.71%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.03% 93.40%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.94% 99.23%
CHEMBL1871 P10275 Androgen Receptor 83.78% 96.43%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.70% 93.04%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.10% 97.14%
CHEMBL233 P35372 Mu opioid receptor 82.03% 97.93%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.51% 89.00%
CHEMBL2095194 P08709 Coagulation factor VII/tissue factor 80.93% 99.17%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.71% 86.00%
CHEMBL321 P14780 Matrix metalloproteinase 9 80.53% 92.12%

Plants that contains it

Top
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.
Balakata baccata

Cross-Links

Top
PubChem 162916679
LOTUS LTS0122713
wikiData Q105254473