Grifolin

Details

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Internal ID 656a8991-2a38-4fc9-b3ed-5af2492086ca
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 5-methyl-2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]benzene-1,3-diol
SMILES (Canonical) CC1=CC(=C(C(=C1)O)CC=C(C)CCC=C(C)CCC=C(C)C)O
SMILES (Isomeric) CC1=CC(=C(C(=C1)O)C/C=C(\C)/CC/C=C(\C)/CCC=C(C)C)O
InChI InChI=1S/C22H32O2/c1-16(2)8-6-9-17(3)10-7-11-18(4)12-13-20-21(23)14-19(5)15-22(20)24/h8,10,12,14-15,23-24H,6-7,9,11,13H2,1-5H3/b17-10+,18-12+
InChI Key PZHNKNRPGLTZPO-VZRGJMDUSA-N
Popularity 92 references in papers

Physical and Chemical Properties

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Molecular Formula C22H32O2
Molecular Weight 328.50 g/mol
Exact Mass 328.240230259 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 7.20
Atomic LogP (AlogP) 6.37
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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6903-07-7
Grifolinterpenoid
5-methyl-2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]benzene-1,3-diol
2-Farnesyl-5-methylresorcinol
CHEMBL487804
SCHEMBL21065400
CHEBI:170125
PZHNKNRPGLTZPO-VZRGJMDUSA-N
DTXSID401044417
BDBM50458916
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Grifolin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.8242 82.42%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7293 72.93%
OATP2B1 inhibitior - 0.7134 71.34%
OATP1B1 inhibitior + 0.8981 89.81%
OATP1B3 inhibitior + 0.9216 92.16%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.4826 48.26%
P-glycoprotein inhibitior - 0.4323 43.23%
P-glycoprotein substrate - 0.9585 95.85%
CYP3A4 substrate - 0.6054 60.54%
CYP2C9 substrate - 0.7887 78.87%
CYP2D6 substrate + 0.3876 38.76%
CYP3A4 inhibition + 0.6702 67.02%
CYP2C9 inhibition + 0.5476 54.76%
CYP2C19 inhibition + 0.5851 58.51%
CYP2D6 inhibition - 0.8163 81.63%
CYP1A2 inhibition + 0.8349 83.49%
CYP2C8 inhibition - 0.8756 87.56%
CYP inhibitory promiscuity + 0.7659 76.59%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7739 77.39%
Carcinogenicity (trinary) Non-required 0.7074 70.74%
Eye corrosion - 0.9205 92.05%
Eye irritation - 0.6322 63.22%
Skin irritation - 0.6342 63.42%
Skin corrosion - 0.7970 79.70%
Ames mutagenesis - 0.6244 62.44%
Human Ether-a-go-go-Related Gene inhibition + 0.8181 81.81%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.7763 77.63%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.7336 73.36%
Acute Oral Toxicity (c) III 0.7001 70.01%
Estrogen receptor binding + 0.6039 60.39%
Androgen receptor binding + 0.5617 56.17%
Thyroid receptor binding + 0.7027 70.27%
Glucocorticoid receptor binding + 0.5747 57.47%
Aromatase binding + 0.5932 59.32%
PPAR gamma + 0.8622 86.22%
Honey bee toxicity - 0.9183 91.83%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9972 99.72%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.99% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.78% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 94.38% 94.73%
CHEMBL2581 P07339 Cathepsin D 90.09% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 89.73% 91.49%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.24% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.79% 99.17%

Cross-Links

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PubChem 5372312
NPASS NPC12640
LOTUS LTS0270847
wikiData Q15634172