1-Methoxy-1-(2,4,5-trimethoxyphenyl)-2-propanol

Details

Top
Internal ID c5841849-e989-4721-a135-530bcd7df49a
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name 1-methoxy-1-(2,4,5-trimethoxyphenyl)propan-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H20O5/c1-8(14)13(18-5)9-6-11(16-3)12(17-4)7-10(9)15-2/h6-8,13-14H,1-5H3
InChI Key IXNRGYSRFBDZLB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H20O5
Molecular Weight 256.29 g/mol
Exact Mass 256.13107373 g/mol
Topological Polar Surface Area (TPSA) 57.20 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.78
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

Top
CHEBI:172498
DTXSID201262889
beta,2,4,5-Tetramethoxy-alpha-methylbenzeneethanol
1-METHOXY-1-(2,4,5-TRIMETHOXYPHENYL)PROPAN-2-OL
98205-47-1

2D Structure

Top
2D Structure of 1-Methoxy-1-(2,4,5-trimethoxyphenyl)-2-propanol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9822 98.22%
Caco-2 + 0.8633 86.33%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8262 82.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9017 90.17%
OATP1B3 inhibitior + 0.9743 97.43%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7863 78.63%
P-glycoprotein inhibitior - 0.8996 89.96%
P-glycoprotein substrate - 0.8804 88.04%
CYP3A4 substrate - 0.6766 67.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4119 41.19%
CYP3A4 inhibition - 0.8694 86.94%
CYP2C9 inhibition - 0.9924 99.24%
CYP2C19 inhibition - 0.8607 86.07%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition - 0.7735 77.35%
CYP2C8 inhibition - 0.9303 93.03%
CYP inhibitory promiscuity - 0.7873 78.73%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7550 75.50%
Carcinogenicity (trinary) Non-required 0.6154 61.54%
Eye corrosion + 0.5237 52.37%
Eye irritation - 0.6644 66.44%
Skin irritation + 0.5505 55.05%
Skin corrosion - 0.9130 91.30%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6502 65.02%
Micronuclear - 0.6467 64.67%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.6669 66.69%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6014 60.14%
Acute Oral Toxicity (c) III 0.6473 64.73%
Estrogen receptor binding - 0.5861 58.61%
Androgen receptor binding - 0.8261 82.61%
Thyroid receptor binding + 0.5595 55.95%
Glucocorticoid receptor binding - 0.7187 71.87%
Aromatase binding - 0.7803 78.03%
PPAR gamma + 0.6451 64.51%
Honey bee toxicity - 0.8644 86.44%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.7813 78.13%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.83% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.71% 85.14%
CHEMBL2581 P07339 Cathepsin D 87.03% 98.95%
CHEMBL4208 P20618 Proteasome component C5 84.06% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.48% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.01% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.31% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.81% 86.33%
CHEMBL2535 P11166 Glucose transporter 80.14% 98.75%

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.
Acorus calamus

Cross-Links

Top
PubChem 131751190
LOTUS LTS0095725
wikiData Q105122297