Oblongolide L

Details

Top
Internal ID 26504252-8e52-405b-b88e-f0be2f624199
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name [(1R,3aS,5aR,7S,9aS,9bR)-1-acetyl-1-butoxy-9b-methyl-3,3a,5a,6,7,8,9,9a-octahydrobenzo[e][2]benzofuran-7-yl]methyl acetate
SMILES (Canonical) CCCCOC1(C2(C3CCC(CC3C=CC2CO1)COC(=O)C)C)C(=O)C
SMILES (Isomeric) CCCCO[C@@]1([C@@]2([C@H]3CC[C@@H](C[C@@H]3C=C[C@@H]2CO1)COC(=O)C)C)C(=O)C
InChI InChI=1S/C22H34O5/c1-5-6-11-26-22(15(2)23)21(4)19(14-27-22)9-8-18-12-17(7-10-20(18)21)13-25-16(3)24/h8-9,17-20H,5-7,10-14H2,1-4H3/t17-,18-,19+,20-,21-,22-/m0/s1
InChI Key APCAFEWMEZLZJS-GVUKCBQMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C22H34O5
Molecular Weight 378.50 g/mol
Exact Mass 378.24062418 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.91
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

Top
((1R,3AS,5ar,7S,9as,9BR)-1-acetyl-1-butoxy-9b-methyl-1H,3H,3ah,5ah,6H,7H,8H,9H,9ah,9BH-naphtho(1,2-c)furan-7-yl)methyl acetic acid
((1R,3aS,5aR,7S,9aS,9bR)-1-acetyl-1-butoxy-9b-methyl-3,3a,5a,6,7,8,9,9a-octahydrobenzo(e)(2)benzofuran-7-yl)methyl acetate
[(1R,3AS,5ar,7S,9as,9BR)-1-acetyl-1-butoxy-9b-methyl-1H,3H,3ah,5ah,6H,7H,8H,9H,9ah,9BH-naphtho[1,2-c]furan-7-yl]methyl acetic acid
[(1R,3aS,5aR,7S,9aS,9bR)-1-acetyl-1-butoxy-9b-methyl-3,3a,5a,6,7,8,9,9a-octahydrobenzo[e][2]benzofuran-7-yl]methyl acetate
RefChem:167375
CHEBI:217692
[(1R,3aS,5aR,7S,9aS,9bR)-1-acetyl-1-butoxy-9b-methyl-3,3a,5a,6,7,8,9,9a-octahydrobenzo[e][2]benzouran-7-yl]methyl acetate

2D Structure

Top
2D Structure of Oblongolide L

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.6770 67.70%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.6918 69.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8195 81.95%
OATP1B3 inhibitior + 0.9616 96.16%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9435 94.35%
P-glycoprotein inhibitior + 0.6188 61.88%
P-glycoprotein substrate - 0.6304 63.04%
CYP3A4 substrate + 0.6849 68.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8796 87.96%
CYP3A4 inhibition - 0.6737 67.37%
CYP2C9 inhibition - 0.8705 87.05%
CYP2C19 inhibition - 0.6304 63.04%
CYP2D6 inhibition - 0.9247 92.47%
CYP1A2 inhibition - 0.9131 91.31%
CYP2C8 inhibition + 0.6470 64.70%
CYP inhibitory promiscuity - 0.6722 67.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5749 57.49%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.9650 96.50%
Skin irritation - 0.6256 62.56%
Skin corrosion - 0.9386 93.86%
Ames mutagenesis - 0.6374 63.74%
Human Ether-a-go-go-Related Gene inhibition + 0.7149 71.49%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.6446 64.46%
skin sensitisation - 0.9134 91.34%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5884 58.84%
Acute Oral Toxicity (c) III 0.5669 56.69%
Estrogen receptor binding + 0.8637 86.37%
Androgen receptor binding + 0.6138 61.38%
Thyroid receptor binding + 0.6003 60.03%
Glucocorticoid receptor binding + 0.6890 68.90%
Aromatase binding + 0.6096 60.96%
PPAR gamma - 0.5642 56.42%
Honey bee toxicity - 0.8838 88.38%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9947 99.47%

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 98.54% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.26% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.54% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.43% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.18% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.04% 99.17%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 88.46% 89.05%
CHEMBL340 P08684 Cytochrome P450 3A4 86.91% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.87% 92.62%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.68% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.30% 86.33%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 85.34% 90.75%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.92% 95.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.91% 95.89%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 83.99% 96.00%
CHEMBL2581 P07339 Cathepsin D 83.69% 98.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.29% 94.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.15% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.21% 96.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.91% 93.56%

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.
There are no matching plants.

Cross-Links

Top
PubChem 11545346
LOTUS LTS0148448
wikiData Q77500919