Shahamin K

Details

Top
Internal ID 185573d0-c3bb-4ed4-bbc0-16e39e1e02d3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name [(4R,5R)-5-[(1R,2S)-2-acetyloxy-1,4,4-trimethyl-8-methylidene-3,3a,5,6,7,8a-hexahydro-2H-azulen-1-yl]-2-oxooxan-4-yl]methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H36O6/c1-14-8-7-9-23(4,5)18-11-20(30-16(3)26)24(6,22(14)18)19-13-29-21(27)10-17(19)12-28-15(2)25/h17-20,22H,1,7-13H2,2-6H3/t17-,18?,19+,20-,22?,24+/m0/s1
InChI Key RETZLADXQSPAKA-UUUCTLAWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C24H36O6
Molecular Weight 420.50 g/mol
Exact Mass 420.25118886 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.07
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Shahamin K

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9761 97.61%
Caco-2 + 0.5642 56.42%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8048 80.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8397 83.97%
OATP1B3 inhibitior + 0.8361 83.61%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.6860 68.60%
P-glycoprotein inhibitior + 0.6665 66.65%
P-glycoprotein substrate - 0.6896 68.96%
CYP3A4 substrate + 0.6580 65.80%
CYP2C9 substrate - 0.8156 81.56%
CYP2D6 substrate - 0.8662 86.62%
CYP3A4 inhibition - 0.8066 80.66%
CYP2C9 inhibition - 0.7947 79.47%
CYP2C19 inhibition - 0.7577 75.77%
CYP2D6 inhibition - 0.9390 93.90%
CYP1A2 inhibition - 0.7515 75.15%
CYP2C8 inhibition + 0.5379 53.79%
CYP inhibitory promiscuity - 0.8197 81.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6539 65.39%
Eye corrosion - 0.9831 98.31%
Eye irritation - 0.8815 88.15%
Skin irritation - 0.6559 65.59%
Skin corrosion - 0.9383 93.83%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4238 42.38%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5161 51.61%
skin sensitisation - 0.7480 74.80%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6348 63.48%
Acute Oral Toxicity (c) III 0.5696 56.96%
Estrogen receptor binding + 0.8126 81.26%
Androgen receptor binding + 0.6432 64.32%
Thyroid receptor binding + 0.6419 64.19%
Glucocorticoid receptor binding + 0.8306 83.06%
Aromatase binding + 0.6323 63.23%
PPAR gamma + 0.6864 68.64%
Honey bee toxicity - 0.6957 69.57%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9954 99.54%

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 98.60% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.43% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.21% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.29% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.62% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.00% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.23% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.79% 100.00%
CHEMBL2581 P07339 Cathepsin D 89.03% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 88.50% 83.82%
CHEMBL2996 Q05655 Protein kinase C delta 88.12% 97.79%
CHEMBL340 P08684 Cytochrome P450 3A4 87.39% 91.19%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.76% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.46% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.02% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.42% 93.04%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.76% 92.62%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.10% 97.28%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.08% 95.50%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 80.89% 89.05%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.74% 95.89%
CHEMBL255 P29275 Adenosine A2b receptor 80.20% 98.59%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 101111080
LOTUS LTS0193091
wikiData Q105235103