Grandilobatin B

Details

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Internal ID 5a54d99f-2a43-48ec-9e80-43174b513d1b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,4E,9S,12E,14S)-12-(2-hydroxypropan-2-yl)-1,5,9-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,12-dien-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O3/c1-14-7-6-10-20(5)18(23-20)13-16(19(3,4)22)9-8-15(2)12-17(21)11-14/h7,13,15,18,22H,6,8-12H2,1-5H3/b14-7+,16-13+/t15-,18-,20-/m0/s1
InChI Key IRGVGKNVASOSJW-FCECOGMUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O3
Molecular Weight 320.50 g/mol
Exact Mass 320.23514488 g/mol
Topological Polar Surface Area (TPSA) 49.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 4.35
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL483696

2D Structure

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2D Structure of Grandilobatin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.7313 73.13%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6832 68.32%
OATP2B1 inhibitior - 0.8637 86.37%
OATP1B1 inhibitior + 0.8979 89.79%
OATP1B3 inhibitior + 0.9678 96.78%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.6001 60.01%
P-glycoprotein inhibitior - 0.8126 81.26%
P-glycoprotein substrate - 0.7410 74.10%
CYP3A4 substrate + 0.6480 64.80%
CYP2C9 substrate - 0.8125 81.25%
CYP2D6 substrate - 0.8069 80.69%
CYP3A4 inhibition - 0.6988 69.88%
CYP2C9 inhibition - 0.5704 57.04%
CYP2C19 inhibition - 0.5724 57.24%
CYP2D6 inhibition - 0.9294 92.94%
CYP1A2 inhibition + 0.5880 58.80%
CYP2C8 inhibition + 0.5614 56.14%
CYP inhibitory promiscuity - 0.9236 92.36%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5796 57.96%
Eye corrosion - 0.9682 96.82%
Eye irritation - 0.9320 93.20%
Skin irritation + 0.5078 50.78%
Skin corrosion - 0.9422 94.22%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3963 39.63%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.6802 68.02%
skin sensitisation + 0.5622 56.22%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.6441 64.41%
Acute Oral Toxicity (c) III 0.6580 65.80%
Estrogen receptor binding - 0.6048 60.48%
Androgen receptor binding - 0.6049 60.49%
Thyroid receptor binding + 0.6565 65.65%
Glucocorticoid receptor binding + 0.6938 69.38%
Aromatase binding - 0.6974 69.74%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.8242 82.42%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9281 92.81%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.49% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.82% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.53% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.84% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.75% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.59% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.68% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.34% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.71% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.55% 95.89%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.93% 86.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.37% 93.04%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.92% 97.14%
CHEMBL1902 P62942 FK506-binding protein 1A 82.16% 97.05%
CHEMBL5028 O14672 ADAM10 81.84% 97.50%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.42% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.09% 96.77%

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 24899405
LOTUS LTS0188896
wikiData Q105118826