Elansolid A

Details

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Internal ID 05f44f81-350a-4eee-8d7c-f7bf7631b25f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name (1R,2Z,4E,6Z,8R,9R,10R,12E,14E,19S,20R,23R,24R)-8,10,23-trihydroxy-18-(4-hydroxyphenyl)-9,13,21,21,23,26-hexamethyl-17-oxatricyclo[17.7.0.020,24]hexacosa-2,4,6,12,14,25-hexaen-16-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H48O6/c1-23-13-19-31(40)25(3)30(39)12-10-8-7-9-11-28-24(2)21-29-34(36(4,5)22-37(29,6)42)33(28)35(43-32(41)20-14-23)26-15-17-27(38)18-16-26/h7-18,20-21,25,28-31,33-35,38-40,42H,19,22H2,1-6H3/b8-7+,11-9-,12-10-,20-14+,23-13+/t25-,28-,29+,30+,31+,33+,34-,35?,37+/m0/s1
InChI Key NTNBXVJSAMSCRI-DJBQPULXSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C37H48O6
Molecular Weight 588.80 g/mol
Exact Mass 588.34508925 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 6.51
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Elansolid A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 - 0.7949 79.49%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.5769 57.69%
OATP2B1 inhibitior - 0.7126 71.26%
OATP1B1 inhibitior + 0.7810 78.10%
OATP1B3 inhibitior + 0.9269 92.69%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9816 98.16%
P-glycoprotein inhibitior + 0.7346 73.46%
P-glycoprotein substrate + 0.5711 57.11%
CYP3A4 substrate + 0.7123 71.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8685 86.85%
CYP3A4 inhibition - 0.6453 64.53%
CYP2C9 inhibition - 0.6125 61.25%
CYP2C19 inhibition - 0.5832 58.32%
CYP2D6 inhibition - 0.8851 88.51%
CYP1A2 inhibition - 0.6873 68.73%
CYP2C8 inhibition + 0.6467 64.67%
CYP inhibitory promiscuity + 0.5921 59.21%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4073 40.73%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.9152 91.52%
Skin irritation - 0.5985 59.85%
Skin corrosion - 0.9188 91.88%
Ames mutagenesis + 0.5146 51.46%
Human Ether-a-go-go-Related Gene inhibition + 0.9099 90.99%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.7106 71.06%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.8495 84.95%
Acute Oral Toxicity (c) I 0.5702 57.02%
Estrogen receptor binding + 0.7714 77.14%
Androgen receptor binding + 0.6930 69.30%
Thyroid receptor binding + 0.6596 65.96%
Glucocorticoid receptor binding + 0.7845 78.45%
Aromatase binding + 0.5958 59.58%
PPAR gamma + 0.7260 72.60%
Honey bee toxicity - 0.7495 74.95%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9933 99.33%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.13% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.11% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.84% 98.95%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 92.29% 90.93%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.81% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 91.76% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.63% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.93% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 89.47% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.21% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.58% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.78% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.30% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 83.02% 97.79%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.58% 94.00%
CHEMBL4523377 Q86WV6 Stimulator of interferon genes protein 80.52% 95.48%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 102191533
LOTUS LTS0129786
wikiData Q77517190