Kansenone

Details

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Internal ID d7c5b7b4-29a9-4f3f-8d06-57a25a6c16b4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (3S,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H48O2/c1-19(2)10-9-11-20(3)21-12-17-30(8)26-22(13-16-29(21,30)7)28(6)15-14-25(32)27(4,5)24(28)18-23(26)31/h10,20-21,24-25,32H,9,11-18H2,1-8H3/t20-,21+,24+,25+,28-,29+,30-/m1/s1
InChI Key TVMGQCAMNPECHD-KUABDJQUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O2
Molecular Weight 440.70 g/mol
Exact Mass 440.365430770 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 8.00
Atomic LogP (AlogP) 7.66
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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543691-16-3
(3S,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one
(3S,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-17-((2R)-6-methylhept-5-en-2-yl)-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta(a)phenanthren-7-one
RefChem:150911
CHEMBL469279
orb1942777
SCHEMBL3229515

2D Structure

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2D Structure of Kansenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6843 68.43%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7532 75.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8107 81.07%
OATP1B3 inhibitior + 0.9598 95.98%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.9376 93.76%
P-glycoprotein inhibitior + 0.6057 60.57%
P-glycoprotein substrate - 0.7371 73.71%
CYP3A4 substrate + 0.6448 64.48%
CYP2C9 substrate - 0.7411 74.11%
CYP2D6 substrate - 0.8673 86.73%
CYP3A4 inhibition - 0.8812 88.12%
CYP2C9 inhibition - 0.8992 89.92%
CYP2C19 inhibition - 0.7207 72.07%
CYP2D6 inhibition - 0.9541 95.41%
CYP1A2 inhibition - 0.9332 93.32%
CYP2C8 inhibition - 0.7596 75.96%
CYP inhibitory promiscuity - 0.7097 70.97%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5654 56.54%
Eye corrosion - 0.9941 99.41%
Eye irritation - 0.9317 93.17%
Skin irritation + 0.6455 64.55%
Skin corrosion - 0.9643 96.43%
Ames mutagenesis - 0.7737 77.37%
Human Ether-a-go-go-Related Gene inhibition - 0.3827 38.27%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.7020 70.20%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.7015 70.15%
Acute Oral Toxicity (c) III 0.8265 82.65%
Estrogen receptor binding + 0.8030 80.30%
Androgen receptor binding + 0.7401 74.01%
Thyroid receptor binding + 0.7927 79.27%
Glucocorticoid receptor binding + 0.8531 85.31%
Aromatase binding + 0.7966 79.66%
PPAR gamma + 0.6753 67.53%
Honey bee toxicity - 0.7610 76.10%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9897 98.97%

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
CHEMBL2581 P07339 Cathepsin D 98.27% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.17% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.23% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.86% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.47% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 88.85% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.38% 97.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.45% 93.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.03% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.99% 93.56%
CHEMBL3038469 P24941 CDK2/Cyclin A 83.83% 91.38%
CHEMBL226 P30542 Adenosine A1 receptor 83.28% 95.93%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.15% 90.71%
CHEMBL1902 P62942 FK506-binding protein 1A 83.01% 97.05%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.75% 82.69%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.51% 93.03%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.48% 90.08%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.37% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.22% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.75% 89.00%
CHEMBL221 P23219 Cyclooxygenase-1 80.46% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.43% 85.14%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 80.19% 98.33%
CHEMBL1907 P15144 Aminopeptidase N 80.04% 93.31%

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.
Euphorbia kansui

Cross-Links

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PubChem 21629615
NPASS NPC86319
LOTUS LTS0133454
wikiData Q105265397