(1R,2R,13R,15R)-8-chloro-11-hydroxy-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadeca-8,10-dien-12-one

Details

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Internal ID ad9d3a26-d150-4c51-9192-2940ae42854f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,2R,13R,15R)-8-chloro-11-hydroxy-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadeca-8,10-dien-12-one
SMILES (Canonical) CC1CC2C3CCCN4C3(C1)C(=C(C2=O)O)C=C(C4)Cl
SMILES (Isomeric) C[C@@H]1C[C@@H]2[C@H]3CCCN4[C@@]3(C1)C(=C(C2=O)O)C=C(C4)Cl
InChI InChI=1S/C16H20ClNO2/c1-9-5-11-12-3-2-4-18-8-10(17)6-13(15(20)14(11)19)16(12,18)7-9/h6,9,11-12,20H,2-5,7-8H2,1H3/t9-,11-,12-,16-/m1/s1
InChI Key GNHFOJPTLHAKDZ-UBEDBUPSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20ClNO2
Molecular Weight 293.79 g/mol
Exact Mass 293.1182566 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2R,13R,15R)-8-chloro-11-hydroxy-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadeca-8,10-dien-12-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9893 98.93%
Caco-2 + 0.8864 88.64%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6894 68.94%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8761 87.61%
OATP1B3 inhibitior + 0.9466 94.66%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.7855 78.55%
P-glycoprotein inhibitior - 0.9251 92.51%
P-glycoprotein substrate - 0.6618 66.18%
CYP3A4 substrate + 0.6449 64.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7464 74.64%
CYP3A4 inhibition - 0.7726 77.26%
CYP2C9 inhibition - 0.6988 69.88%
CYP2C19 inhibition - 0.7347 73.47%
CYP2D6 inhibition - 0.6297 62.97%
CYP1A2 inhibition - 0.7307 73.07%
CYP2C8 inhibition - 0.7933 79.33%
CYP inhibitory promiscuity - 0.7519 75.19%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Danger 0.4434 44.34%
Eye corrosion - 0.9822 98.22%
Eye irritation - 0.9767 97.67%
Skin irritation - 0.6873 68.73%
Skin corrosion - 0.8903 89.03%
Ames mutagenesis - 0.6578 65.78%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.6869 68.69%
skin sensitisation - 0.7791 77.91%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.6720 67.20%
Acute Oral Toxicity (c) III 0.5836 58.36%
Estrogen receptor binding + 0.5709 57.09%
Androgen receptor binding + 0.6576 65.76%
Thyroid receptor binding + 0.6463 64.63%
Glucocorticoid receptor binding + 0.8735 87.35%
Aromatase binding + 0.6134 61.34%
PPAR gamma + 0.6307 63.07%
Honey bee toxicity - 0.8902 89.02%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.8018 80.18%

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%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.87% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.34% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.24% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.19% 94.45%
CHEMBL2581 P07339 Cathepsin D 87.70% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.58% 96.09%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 86.94% 94.78%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.89% 95.89%
CHEMBL1871 P10275 Androgen Receptor 86.11% 96.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.96% 100.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 85.42% 83.57%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.45% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.58% 86.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.25% 93.40%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.62% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.57% 90.71%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.91% 95.50%
CHEMBL332 P03956 Matrix metalloproteinase-1 80.74% 94.50%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.60% 82.69%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 80.43% 95.27%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.24% 92.94%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.16% 93.03%

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.
Huperzia serrata

Cross-Links

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PubChem 163027105
LOTUS LTS0152617
wikiData Q105012512