Folinin

Details

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Internal ID 14ff5b6f-a478-495b-ba53-87bb0d677e63
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Furanoisoflavonoids > Pterocarpans
IUPAC Name 7,7,20,20-tetramethyl-8,12,19,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosa-2(11),3,9,15(24),16,18(23),21-heptaene
SMILES (Canonical) CC1(CCC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC6=C5C=CC(O6)(C)C)C
SMILES (Isomeric) CC1(CCC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC6=C5C=CC(O6)(C)C)C
InChI InChI=1S/C25H26O4/c1-24(2)9-7-14-11-17-21(12-20(14)29-24)26-13-18-15-5-6-19-16(22(15)27-23(17)18)8-10-25(3,4)28-19/h5-6,8,10-12,18,23H,7,9,13H2,1-4H3
InChI Key GIJCKIAEOVPFOW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H26O4
Molecular Weight 390.50 g/mol
Exact Mass 390.18310931 g/mol
Topological Polar Surface Area (TPSA) 36.90 Ų
XlogP 4.90
Atomic LogP (AlogP) 5.58
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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LMPK12070024

2D Structure

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2D Structure of Folinin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.7460 74.60%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7126 71.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8933 89.33%
OATP1B3 inhibitior + 0.9603 96.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9574 95.74%
P-glycoprotein inhibitior + 0.8419 84.19%
P-glycoprotein substrate + 0.5466 54.66%
CYP3A4 substrate + 0.6447 64.47%
CYP2C9 substrate + 0.5918 59.18%
CYP2D6 substrate + 0.3583 35.83%
CYP3A4 inhibition - 0.6671 66.71%
CYP2C9 inhibition - 0.6442 64.42%
CYP2C19 inhibition - 0.5765 57.65%
CYP2D6 inhibition - 0.7229 72.29%
CYP1A2 inhibition + 0.6633 66.33%
CYP2C8 inhibition + 0.5689 56.89%
CYP inhibitory promiscuity + 0.5959 59.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.5295 52.95%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.7218 72.18%
Skin irritation - 0.7861 78.61%
Skin corrosion - 0.9473 94.73%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7010 70.10%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5769 57.69%
skin sensitisation - 0.6808 68.08%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6828 68.28%
Acute Oral Toxicity (c) III 0.6836 68.36%
Estrogen receptor binding + 0.9174 91.74%
Androgen receptor binding + 0.6941 69.41%
Thyroid receptor binding + 0.7240 72.40%
Glucocorticoid receptor binding + 0.8279 82.79%
Aromatase binding - 0.5273 52.73%
PPAR gamma + 0.8321 83.21%
Honey bee toxicity - 0.7459 74.59%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9672 96.72%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.88% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 95.14% 92.51%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.06% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.44% 94.45%
CHEMBL2581 P07339 Cathepsin D 92.93% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 92.92% 93.40%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.91% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.90% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.30% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.03% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.04% 100.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 87.87% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.51% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.12% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.89% 93.99%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.84% 93.56%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 82.97% 81.29%
CHEMBL226 P30542 Adenosine A1 receptor 81.22% 95.93%
CHEMBL1907 P15144 Aminopeptidase N 81.14% 93.31%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.72% 89.00%

Plants that contains it

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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.
Almeidea rubra

Cross-Links

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PubChem 44257438
LOTUS LTS0246823
wikiData Q105009024