17-Norkauran-16-one

Details

Top
Internal ID 53eb3543-1e12-421c-ab48-3f68fa39f2ff
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name (1S,4R,9R,10R,13R)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-one
SMILES (Canonical) CC1(CCCC2(C1CCC34C2CCC(C3)C(=O)C4)C)C
SMILES (Isomeric) C[C@@]12CCCC([C@H]1CC[C@]34[C@H]2CC[C@H](C3)C(=O)C4)(C)C
InChI InChI=1S/C19H30O/c1-17(2)8-4-9-18(3)15(17)7-10-19-11-13(14(20)12-19)5-6-16(18)19/h13,15-16H,4-12H2,1-3H3/t13-,15-,16+,18-,19+/m1/s1
InChI Key JJFSSTSAIZSCOF-HSAPRAMBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C19H30O
Molecular Weight 274.40 g/mol
Exact Mass 274.229665576 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.99
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 17-Norkauran-16-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.6941 69.41%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.4856 48.56%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9238 92.38%
OATP1B3 inhibitior + 0.9822 98.22%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7066 70.66%
P-glycoprotein inhibitior - 0.8061 80.61%
P-glycoprotein substrate - 0.8990 89.90%
CYP3A4 substrate + 0.5894 58.94%
CYP2C9 substrate - 0.7707 77.07%
CYP2D6 substrate - 0.7734 77.34%
CYP3A4 inhibition - 0.9458 94.58%
CYP2C9 inhibition - 0.7557 75.57%
CYP2C19 inhibition - 0.7744 77.44%
CYP2D6 inhibition - 0.9637 96.37%
CYP1A2 inhibition - 0.8592 85.92%
CYP2C8 inhibition - 0.8527 85.27%
CYP inhibitory promiscuity - 0.9526 95.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6009 60.09%
Eye corrosion - 0.9276 92.76%
Eye irritation - 0.6012 60.12%
Skin irritation + 0.6002 60.02%
Skin corrosion - 0.9173 91.73%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5183 51.83%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation + 0.7613 76.13%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.7396 73.96%
Acute Oral Toxicity (c) III 0.8058 80.58%
Estrogen receptor binding + 0.7545 75.45%
Androgen receptor binding - 0.5166 51.66%
Thyroid receptor binding + 0.5468 54.68%
Glucocorticoid receptor binding + 0.6692 66.92%
Aromatase binding + 0.5535 55.35%
PPAR gamma - 0.6718 67.18%
Honey bee toxicity - 0.8516 85.16%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9518 95.18%

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 97.53% 97.25%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 96.34% 96.38%
CHEMBL1937 Q92769 Histone deacetylase 2 90.36% 94.75%
CHEMBL2581 P07339 Cathepsin D 88.03% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.32% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.15% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.89% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.83% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.78% 95.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.06% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.27% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.01% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.98% 96.09%
CHEMBL1902 P62942 FK506-binding protein 1A 81.55% 97.05%
CHEMBL3524 P56524 Histone deacetylase 4 81.38% 92.97%
CHEMBL3012 Q13946 Phosphodiesterase 7A 81.17% 99.29%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 81.04% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 80.67% 92.50%

Cross-Links

Top
PubChem 12112097
NPASS NPC146657
LOTUS LTS0136963
wikiData Q105129636