Sacidumlignan A

Details

Top
Internal ID 4715d6d9-568c-44c1-9b4c-2c7c97fa7743
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 5-(4-hydroxy-3,5-dimethoxyphenyl)-1,3-dimethoxy-6,7-dimethylnaphthalen-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24O6/c1-11-7-15-14(10-18(27-5)21(24)22(15)28-6)19(12(11)2)13-8-16(25-3)20(23)17(9-13)26-4/h7-10,23-24H,1-6H3
InChI Key NBOWNYPCCMRIJM-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

Top
Molecular Formula C22H24O6
Molecular Weight 384.40 g/mol
Exact Mass 384.15728848 g/mol
Topological Polar Surface Area (TPSA) 77.40 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.57
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

Top
CHEMBL497087
5-(4-hydroxy-3,5-dimethoxyphenyl)-1,3-dimethoxy-6,7-dimethylnaphthalen-2-ol

2D Structure

Top
2D Structure of Sacidumlignan A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.7494 74.94%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8037 80.37%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.8815 88.15%
OATP1B3 inhibitior + 0.8818 88.18%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7846 78.46%
P-glycoprotein inhibitior - 0.5895 58.95%
P-glycoprotein substrate - 0.8145 81.45%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate + 0.4558 45.58%
CYP3A4 inhibition - 0.7586 75.86%
CYP2C9 inhibition - 0.6456 64.56%
CYP2C19 inhibition + 0.5359 53.59%
CYP2D6 inhibition - 0.8730 87.30%
CYP1A2 inhibition + 0.8383 83.83%
CYP2C8 inhibition + 0.6595 65.95%
CYP inhibitory promiscuity + 0.6860 68.60%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.4770 47.70%
Eye corrosion - 0.9885 98.85%
Eye irritation + 0.9309 93.09%
Skin irritation - 0.7062 70.62%
Skin corrosion - 0.9579 95.79%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5215 52.15%
Micronuclear + 0.6500 65.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.9064 90.64%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.8917 89.17%
Acute Oral Toxicity (c) III 0.5425 54.25%
Estrogen receptor binding + 0.8978 89.78%
Androgen receptor binding - 0.5928 59.28%
Thyroid receptor binding + 0.8155 81.55%
Glucocorticoid receptor binding + 0.8368 83.68%
Aromatase binding + 0.8296 82.96%
PPAR gamma + 0.7852 78.52%
Honey bee toxicity - 0.9265 92.65%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9666 96.66%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.04% 91.11%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 89.72% 89.32%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.47% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.45% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.87% 99.15%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 86.86% 92.68%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.53% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 85.73% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.24% 96.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.10% 92.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.06% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.65% 89.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.37% 89.62%
CHEMBL290 Q13370 Phosphodiesterase 3B 80.86% 94.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.62% 94.03%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.30% 82.38%
CHEMBL4302 P08183 P-glycoprotein 1 80.15% 92.98%
CHEMBL213 P08588 Beta-1 adrenergic receptor 80.09% 95.56%

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.
There are no matching plants.

Cross-Links

Top
PubChem 11234481
LOTUS LTS0125901
wikiData Q105176896