Globostellatic Acid F Methyl Ester

Details

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Internal ID 40fc00df-5523-427f-8640-3acd99c25dc0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name methyl (3E,3aS,5aR,6R,7R,9aR,9bS)-7-acetyloxy-3-[(3E,5E,7E)-9,10-dihydroxy-6,10-dimethylundeca-3,5,7-trien-2-ylidene]-3a,6,9a-trimethyl-2-oxo-1,4,5,5a,7,8,9,9b-octahydrocyclopenta[a]naphthalene-6-carboxylate
SMILES (Canonical) CC(=CC=CC(=C1C(=O)CC2C1(CCC3C2(CCC(C3(C)C(=O)OC)OC(=O)C)C)C)C)C=CC(C(C)(C)O)O
SMILES (Isomeric) C/C(=C\C=C\C(=C/1\C(=O)C[C@@H]2[C@@]1(CC[C@@H]3[C@@]2(CC[C@H]([C@]3(C)C(=O)OC)OC(=O)C)C)C)\C)/C=C/C(C(C)(C)O)O
InChI InChI=1S/C33H48O7/c1-20(13-14-26(36)30(4,5)38)11-10-12-21(2)28-23(35)19-25-31(6)18-16-27(40-22(3)34)33(8,29(37)39-9)24(31)15-17-32(25,28)7/h10-14,24-27,36,38H,15-19H2,1-9H3/b12-10+,14-13+,20-11+,28-21-/t24-,25+,26?,27-,31+,32+,33-/m1/s1
InChI Key RPQIPTLEYKHMBM-GNHKJRBKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C33H48O7
Molecular Weight 556.70 g/mol
Exact Mass 556.34000387 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.41
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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CHEMBL392829

2D Structure

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2D Structure of Globostellatic Acid F Methyl Ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9813 98.13%
Caco-2 - 0.7582 75.82%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8226 82.26%
OATP2B1 inhibitior - 0.7140 71.40%
OATP1B1 inhibitior + 0.8395 83.95%
OATP1B3 inhibitior + 0.8739 87.39%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9876 98.76%
P-glycoprotein inhibitior + 0.8145 81.45%
P-glycoprotein substrate - 0.5159 51.59%
CYP3A4 substrate + 0.7245 72.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9120 91.20%
CYP3A4 inhibition - 0.8320 83.20%
CYP2C9 inhibition - 0.7991 79.91%
CYP2C19 inhibition - 0.8698 86.98%
CYP2D6 inhibition - 0.9586 95.86%
CYP1A2 inhibition - 0.7239 72.39%
CYP2C8 inhibition + 0.5106 51.06%
CYP inhibitory promiscuity - 0.9643 96.43%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9720 97.20%
Carcinogenicity (trinary) Non-required 0.6103 61.03%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.9199 91.99%
Skin irritation + 0.4932 49.32%
Skin corrosion - 0.9512 95.12%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7705 77.05%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.6446 64.46%
skin sensitisation - 0.7398 73.98%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6822 68.22%
Acute Oral Toxicity (c) I 0.3682 36.82%
Estrogen receptor binding + 0.8268 82.68%
Androgen receptor binding + 0.6021 60.21%
Thyroid receptor binding + 0.6769 67.69%
Glucocorticoid receptor binding + 0.8077 80.77%
Aromatase binding + 0.7044 70.44%
PPAR gamma + 0.6823 68.23%
Honey bee toxicity - 0.6713 67.13%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9947 99.47%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.38% 85.14%
CHEMBL4040 P28482 MAP kinase ERK2 98.02% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.46% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.24% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.61% 94.45%
CHEMBL2581 P07339 Cathepsin D 92.53% 98.95%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 90.79% 91.03%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 90.20% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 89.51% 91.19%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.31% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.65% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.40% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.05% 95.56%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.93% 91.07%
CHEMBL5028 O14672 ADAM10 86.10% 97.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.25% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.66% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.21% 96.77%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.08% 95.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.98% 89.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.57% 91.24%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.46% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.35% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.13% 93.04%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.40% 92.88%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.95% 100.00%
CHEMBL255 P29275 Adenosine A2b receptor 80.08% 98.59%

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 44434367
LOTUS LTS0153056
wikiData Q105242918