Grandilobatin D

Details

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Internal ID 46deade7-0778-4baf-bd53-a47a0081c69a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Cembrane diterpenoids
IUPAC Name (3E,7E,9E,13S)-10-(2-hydroxypropan-2-yl)-3,7,13-trimethylcyclotetradeca-3,7,9-trien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O2/c1-15-7-6-8-16(2)13-19(21)14-17(3)10-12-18(11-9-15)20(4,5)22/h8-9,11,17,22H,6-7,10,12-14H2,1-5H3/b15-9+,16-8+,18-11+/t17-/m0/s1
InChI Key KECRMPBXABTDAG-OKTAHGQMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O2
Molecular Weight 304.50 g/mol
Exact Mass 304.240230259 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.40
Atomic LogP (AlogP) 5.14
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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RefChem:144299
(3E,7E,9E,13S)-10-(2-hydroxypropan-2-yl)-3,7,13-trimethylcyclotetradeca-3,7,9-trien-1-one
1033611-50-5
CHEMBL505373

2D Structure

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2D Structure of Grandilobatin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.8337 83.37%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7492 74.92%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.9352 93.52%
OATP1B3 inhibitior + 0.9576 95.76%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 0.7764 77.64%
P-glycoprotein inhibitior - 0.8177 81.77%
P-glycoprotein substrate - 0.8262 82.62%
CYP3A4 substrate + 0.5388 53.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8320 83.20%
CYP3A4 inhibition - 0.7816 78.16%
CYP2C9 inhibition - 0.7223 72.23%
CYP2C19 inhibition - 0.7012 70.12%
CYP2D6 inhibition - 0.9342 93.42%
CYP1A2 inhibition - 0.6566 65.66%
CYP2C8 inhibition - 0.7475 74.75%
CYP inhibitory promiscuity - 0.9045 90.45%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8728 87.28%
Carcinogenicity (trinary) Non-required 0.5486 54.86%
Eye corrosion - 0.9246 92.46%
Eye irritation - 0.7917 79.17%
Skin irritation + 0.6761 67.61%
Skin corrosion - 0.9720 97.20%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7178 71.78%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7678 76.78%
skin sensitisation + 0.7788 77.88%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5447 54.47%
Acute Oral Toxicity (c) III 0.7700 77.00%
Estrogen receptor binding - 0.7344 73.44%
Androgen receptor binding - 0.5578 55.78%
Thyroid receptor binding + 0.7039 70.39%
Glucocorticoid receptor binding - 0.4917 49.17%
Aromatase binding - 0.7065 70.65%
PPAR gamma + 0.6027 60.27%
Honey bee toxicity - 0.8560 85.60%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9426 94.26%

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 98.55% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.43% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.45% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.32% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.01% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.21% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.47% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.36% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.76% 95.89%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.31% 90.93%

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 44585760
LOTUS LTS0047607
wikiData Q105139877