Lupulone C

Details

Top
Internal ID 5de3671f-f032-4bb6-a5c1-c6570d690c8c
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 4-hydroxy-2-(2-hydroxypropan-2-yl)-7-(3-methylbutanoyl)-5,5-bis(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-6-one
SMILES (Canonical) CC(C)CC(=O)C1=C2C(=C(C(C1=O)(CC=C(C)C)CC=C(C)C)O)CC(O2)C(C)(C)O
SMILES (Isomeric) CC(C)CC(=O)C1=C2C(=C(C(C1=O)(CC=C(C)C)CC=C(C)C)O)CC(O2)C(C)(C)O
InChI InChI=1S/C26H38O5/c1-15(2)9-11-26(12-10-16(3)4)23(28)18-14-20(25(7,8)30)31-22(18)21(24(26)29)19(27)13-17(5)6/h9-10,17,20,28,30H,11-14H2,1-8H3
InChI Key LFIUJFSCSONDPE-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C26H38O5
Molecular Weight 430.60 g/mol
Exact Mass 430.27192431 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 4.60
Atomic LogP (AlogP) 5.51
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

Top
613683-50-4
4-hydroxy-2-(2-hydroxypropan-2-yl)-7-(3-methylbutanoyl)-5,5-bis(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-6-one
RefChem:154358
6-Hydroxy-2-(2-hydroxypropan-2-yl)-5,5-bis(3-methylbut-2-en-1-yl)-7-(3-methylbutanoyl)-2,3-dihydrobenzofuran-4(5H)-one
CHEMBL481840
orb1942863
DA-65112
E88976

2D Structure

Top
2D Structure of Lupulone C

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.5274 52.74%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7546 75.46%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.8365 83.65%
OATP1B3 inhibitior + 0.8980 89.80%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.5565 55.65%
P-glycoprotein inhibitior - 0.5819 58.19%
P-glycoprotein substrate - 0.5535 55.35%
CYP3A4 substrate + 0.6177 61.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8856 88.56%
CYP3A4 inhibition - 0.8746 87.46%
CYP2C9 inhibition - 0.7879 78.79%
CYP2C19 inhibition - 0.8557 85.57%
CYP2D6 inhibition - 0.9298 92.98%
CYP1A2 inhibition - 0.7852 78.52%
CYP2C8 inhibition - 0.7408 74.08%
CYP inhibitory promiscuity - 0.7952 79.52%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5263 52.63%
Eye corrosion - 0.9811 98.11%
Eye irritation - 0.6358 63.58%
Skin irritation - 0.5568 55.68%
Skin corrosion - 0.9004 90.04%
Ames mutagenesis - 0.5582 55.82%
Human Ether-a-go-go-Related Gene inhibition - 0.7164 71.64%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.6524 65.24%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.5342 53.42%
Acute Oral Toxicity (c) III 0.3617 36.17%
Estrogen receptor binding + 0.7622 76.22%
Androgen receptor binding + 0.5663 56.63%
Thyroid receptor binding + 0.5937 59.37%
Glucocorticoid receptor binding + 0.7085 70.85%
Aromatase binding + 0.7207 72.07%
PPAR gamma + 0.8961 89.61%
Honey bee toxicity - 0.8525 85.25%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9753 97.53%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.77% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.19% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.20% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 93.51% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.28% 97.25%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 89.74% 90.93%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.51% 85.14%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.80% 93.56%
CHEMBL2996 Q05655 Protein kinase C delta 86.68% 97.79%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.42% 89.34%
CHEMBL4040 P28482 MAP kinase ERK2 86.37% 83.82%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.98% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.12% 95.56%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 82.84% 96.90%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.70% 97.09%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.28% 100.00%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 81.19% 83.10%

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.
Humulus lupulus

Cross-Links

Top
PubChem 11212586
NPASS NPC267482
LOTUS LTS0109677
wikiData Q105151030