(1S,6S,7S,10S,15R,18S,19R,22S)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.01,6.07,15.010,14.019,22]docos-13-en-4-one

Details

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Internal ID 432cefb1-813c-470b-a8e4-f9d32c52c1f8
Taxonomy Organoheterocyclic compounds > Quinolidines
IUPAC Name (1S,6S,7S,10S,15R,18S,19R,22S)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.01,6.07,15.010,14.019,22]docos-13-en-4-one
SMILES (Canonical) CC1CN2C3C(CCC4C3=CCC4)C5(C6(C2C1CC6)CCC(=O)O5)C
SMILES (Isomeric) C[C@@H]1CN2[C@@H]3[C@H](CC[C@H]4C3=CCC4)[C@]5([C@]6([C@@H]2[C@@H]1CC6)CCC(=O)O5)C
InChI InChI=1S/C22H31NO2/c1-13-12-23-19-16-5-3-4-14(16)6-7-17(19)21(2)22(11-9-18(24)25-21)10-8-15(13)20(22)23/h5,13-15,17,19-20H,3-4,6-12H2,1-2H3/t13-,14+,15-,17+,19+,20+,21+,22+/m1/s1
InChI Key NGQSEZXJVMCXSC-OHFGCKFYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C22H31NO2
Molecular Weight 341.50 g/mol
Exact Mass 341.235479232 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.93
H-Bond Acceptor 3
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 (1S,6S,7S,10S,15R,18S,19R,22S)-6,18-dimethyl-5-oxa-16-azahexacyclo[14.5.1.01,6.07,15.010,14.019,22]docos-13-en-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.7250 72.50%
Blood Brain Barrier + 0.7879 78.79%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6070 60.70%
OATP2B1 inhibitior - 0.8701 87.01%
OATP1B1 inhibitior + 0.8899 88.99%
OATP1B3 inhibitior + 0.9533 95.33%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.5055 50.55%
P-glycoprotein inhibitior - 0.5434 54.34%
P-glycoprotein substrate - 0.6823 68.23%
CYP3A4 substrate + 0.6670 66.70%
CYP2C9 substrate - 0.8119 81.19%
CYP2D6 substrate - 0.7069 70.69%
CYP3A4 inhibition - 0.8405 84.05%
CYP2C9 inhibition - 0.9379 93.79%
CYP2C19 inhibition - 0.8258 82.58%
CYP2D6 inhibition - 0.8009 80.09%
CYP1A2 inhibition - 0.7839 78.39%
CYP2C8 inhibition - 0.7038 70.38%
CYP inhibitory promiscuity - 0.8721 87.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4868 48.68%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.9658 96.58%
Skin irritation - 0.7394 73.94%
Skin corrosion - 0.8950 89.50%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3615 36.15%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.5694 56.94%
skin sensitisation - 0.7482 74.82%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.5215 52.15%
Acute Oral Toxicity (c) III 0.7181 71.81%
Estrogen receptor binding + 0.8452 84.52%
Androgen receptor binding + 0.7174 71.74%
Thyroid receptor binding - 0.5079 50.79%
Glucocorticoid receptor binding + 0.8439 84.39%
Aromatase binding + 0.6204 62.04%
PPAR gamma - 0.5106 51.06%
Honey bee toxicity - 0.8502 85.02%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.9011 90.11%

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 96.82% 97.25%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 96.41% 93.40%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.11% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.92% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.03% 98.95%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.17% 96.38%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.09% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.97% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.96% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.21% 82.69%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.13% 94.80%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 84.64% 94.78%
CHEMBL1871 P10275 Androgen Receptor 84.41% 96.43%
CHEMBL332 P03956 Matrix metalloproteinase-1 83.72% 94.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.44% 97.14%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.28% 86.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.55% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.96% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.40% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.30% 89.00%
CHEMBL4208 P20618 Proteasome component C5 80.25% 90.00%

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.
Daphniphyllum himalayense
Daphniphyllum pentandrum
Daphniphyllum subverticillatum

Cross-Links

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PubChem 162923744
LOTUS LTS0017352
wikiData Q105179106