Excisanin K

Details

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Internal ID d1ea9da7-11f3-428c-8859-896066118cc4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name (1S,4R,5S,8S,9R,10S,13S,16R)-8,16-dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O4/c1-11-12-4-5-14-19(3)13(18(2,10-21)8-7-15(19)22)6-9-20(14,16(11)23)17(12)24/h12-15,17,21-22,24H,1,4-10H2,2-3H3/t12-,13+,14-,15-,17+,18+,19+,20+/m0/s1
InChI Key IOLAXGYDTVZNNV-UGKKBRBKSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O4
Molecular Weight 334.40 g/mol
Exact Mass 334.21440943 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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RefChem:139732
675606-10-7
CHEMBL550435
SCHEMBL29674560

2D Structure

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2D Structure of Excisanin K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.5958 59.58%
Blood Brain Barrier + 0.6855 68.55%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6466 64.66%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.8679 86.79%
OATP1B3 inhibitior + 0.9545 95.45%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.5712 57.12%
BSEP inhibitior - 0.6328 63.28%
P-glycoprotein inhibitior - 0.8245 82.45%
P-glycoprotein substrate - 0.8202 82.02%
CYP3A4 substrate + 0.6061 60.61%
CYP2C9 substrate - 0.8155 81.55%
CYP2D6 substrate - 0.8081 80.81%
CYP3A4 inhibition - 0.8172 81.72%
CYP2C9 inhibition - 0.8331 83.31%
CYP2C19 inhibition - 0.8868 88.68%
CYP2D6 inhibition - 0.9349 93.49%
CYP1A2 inhibition - 0.8743 87.43%
CYP2C8 inhibition - 0.7061 70.61%
CYP inhibitory promiscuity - 0.8842 88.42%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6566 65.66%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.8519 85.19%
Skin irritation - 0.5128 51.28%
Skin corrosion - 0.9539 95.39%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5320 53.20%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6851 68.51%
skin sensitisation - 0.8584 85.84%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6470 64.70%
Acute Oral Toxicity (c) III 0.5518 55.18%
Estrogen receptor binding + 0.8091 80.91%
Androgen receptor binding + 0.6639 66.39%
Thyroid receptor binding + 0.7368 73.68%
Glucocorticoid receptor binding + 0.8355 83.55%
Aromatase binding + 0.7226 72.26%
PPAR gamma - 0.5436 54.36%
Honey bee toxicity - 0.8907 89.07%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6234 62.34%
Fish aquatic toxicity + 0.9912 99.12%

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 95.65% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.51% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.07% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.35% 98.95%
CHEMBL218 P21554 Cannabinoid CB1 receptor 90.59% 96.61%
CHEMBL1937 Q92769 Histone deacetylase 2 86.57% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.96% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.05% 95.89%
CHEMBL226 P30542 Adenosine A1 receptor 83.57% 95.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.73% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.31% 100.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.06% 90.08%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.03% 93.04%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.79% 100.00%
CHEMBL1871 P10275 Androgen Receptor 81.29% 96.43%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.86% 93.00%

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.
Isodon excisus
Isodon scoparius

Cross-Links

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PubChem 45270538
NPASS NPC476168
ChEMBL CHEMBL550435
LOTUS LTS0187737
wikiData Q105116734