Gnaphalidin

Details

Top
Internal ID c05175d1-7844-474b-85c8-87da686f3609
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Dicarboxylic acids and derivatives
IUPAC Name
SMILES (Canonical) CC1CC(=O)C2(C(C13CC(OC3OC(=O)C)C4=COC=C4)CCCC25CO5)COC(=O)C
SMILES (Isomeric) C[C@@H]1CC(=O)[C@@]2([C@@H]([C@@]13C[C@H](O[C@H]3OC(=O)C)C4=COC=C4)CCC[C@]25CO5)COC(=O)C
InChI InChI=1S/C24H30O8/c1-14-9-20(27)24(13-29-15(2)25)19(5-4-7-22(24)12-30-22)23(14)10-18(17-6-8-28-11-17)32-21(23)31-16(3)26/h6,8,11,14,18-19,21H,4-5,7,9-10,12-13H2,1-3H3/t14-,18+,19-,21-,22+,23-,24+/m1/s1
InChI Key GXQZOQHVBGNFHI-CZQCRYLRSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H30O8
Molecular Weight 446.50 g/mol
Exact Mass 446.19406791 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
MEGxp0_000709
ACon0_000193
AKOS040734484
NCGC00380853-01
NCGC00380853-01_C24H30O8_Dispiro[furan-3(2H),1'(5'H)-naphthalene-5',2''-oxiran]-4'(6'H)-one, 2-(acetyloxy)-4'a-[(acetyloxy)methyl]-5-(3-furanyl)octahydro-2'-methyl-, (2S,2'R,3R,4a'S,5S,5'R,8a'R)-

2D Structure

Top
2D Structure of Gnaphalidin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 - 0.6278 62.78%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7953 79.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7644 76.44%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.7176 71.76%
P-glycoprotein inhibitior + 0.6268 62.68%
P-glycoprotein substrate - 0.6046 60.46%
CYP3A4 substrate + 0.6722 67.22%
CYP2C9 substrate - 0.6064 60.64%
CYP2D6 substrate - 0.8406 84.06%
CYP3A4 inhibition - 0.5569 55.69%
CYP2C9 inhibition - 0.6662 66.62%
CYP2C19 inhibition - 0.6283 62.83%
CYP2D6 inhibition - 0.9364 93.64%
CYP1A2 inhibition - 0.8831 88.31%
CYP2C8 inhibition + 0.6193 61.93%
CYP inhibitory promiscuity - 0.7591 75.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5500 55.00%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8997 89.97%
Skin irritation - 0.7750 77.50%
Skin corrosion - 0.9374 93.74%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8424 84.24%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8895 88.95%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.6652 66.52%
Acute Oral Toxicity (c) III 0.4261 42.61%
Estrogen receptor binding + 0.8952 89.52%
Androgen receptor binding + 0.7473 74.73%
Thyroid receptor binding + 0.5158 51.58%
Glucocorticoid receptor binding + 0.8327 83.27%
Aromatase binding + 0.7419 74.19%
PPAR gamma + 0.6299 62.99%
Honey bee toxicity - 0.8356 83.56%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5750 57.50%
Fish aquatic toxicity + 0.9942 99.42%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.54% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.31% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.13% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.30% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.25% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.16% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.09% 82.69%
CHEMBL221 P23219 Cyclooxygenase-1 89.42% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.20% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.10% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.08% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.51% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.50% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.51% 95.71%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.15% 93.04%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.18% 92.62%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 81.15% 96.39%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.35% 95.56%

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.
Teucrium gnaphalodes

Cross-Links

Top
PubChem 23955788
LOTUS LTS0221756
wikiData Q105023308