(1S,2S)-1-(4-methoxyphenyl)propane-1,2-diol

Details

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Internal ID 569ddd7f-c267-4edb-ada6-e685bc64fcb6
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name (1S,2S)-1-(4-methoxyphenyl)propane-1,2-diol
SMILES (Canonical) CC(C(C1=CC=C(C=C1)OC)O)O
SMILES (Isomeric) C[C@@H]([C@H](C1=CC=C(C=C1)OC)O)O
InChI InChI=1S/C10H14O3/c1-7(11)10(12)8-3-5-9(13-2)6-4-8/h3-7,10-12H,1-2H3/t7-,10+/m0/s1
InChI Key MRDZSBVJWOXBRW-OIBJUYFYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O3
Molecular Weight 182.22 g/mol
Exact Mass 182.094294304 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.11
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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(1S,2S)-1-(4-methoxyphenyl)propane-1,2-diol
Anethole glycol
CHEBI:168966
ZB0585
ZB0600
(1S,2S)-1-(4-Methoxyphenyl)-1,2-propanediol

2D Structure

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2D Structure of (1S,2S)-1-(4-methoxyphenyl)propane-1,2-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9813 98.13%
Caco-2 + 0.7105 71.05%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8611 86.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9467 94.67%
OATP1B3 inhibitior + 0.9645 96.45%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9308 93.08%
P-glycoprotein inhibitior - 0.9758 97.58%
P-glycoprotein substrate - 0.9299 92.99%
CYP3A4 substrate - 0.7273 72.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3841 38.41%
CYP3A4 inhibition - 0.9375 93.75%
CYP2C9 inhibition - 0.9202 92.02%
CYP2C19 inhibition - 0.8755 87.55%
CYP2D6 inhibition - 0.9471 94.71%
CYP1A2 inhibition - 0.8339 83.39%
CYP2C8 inhibition - 0.9897 98.97%
CYP inhibitory promiscuity - 0.8955 89.55%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7036 70.36%
Carcinogenicity (trinary) Non-required 0.4945 49.45%
Eye corrosion + 0.5000 50.00%
Eye irritation - 0.7663 76.63%
Skin irritation + 0.7267 72.67%
Skin corrosion - 0.6945 69.45%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5878 58.78%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.6460 64.60%
skin sensitisation + 0.5810 58.10%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.6771 67.71%
Acute Oral Toxicity (c) III 0.9054 90.54%
Estrogen receptor binding - 0.9051 90.51%
Androgen receptor binding - 0.6316 63.16%
Thyroid receptor binding - 0.7616 76.16%
Glucocorticoid receptor binding - 0.8360 83.60%
Aromatase binding - 0.8918 89.18%
PPAR gamma - 0.6652 66.52%
Honey bee toxicity - 0.9647 96.47%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.4254 42.54%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.51% 96.09%
CHEMBL4208 P20618 Proteasome component C5 94.17% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.88% 85.14%
CHEMBL3492 P49721 Proteasome Macropain subunit 88.03% 90.24%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.74% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.61% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.25% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.67% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 82.33% 93.31%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.87% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 81.39% 90.17%

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.
Albizia julibrissin
Anacardium occidentale
Anchusa officinalis
Caryopteris mongholica
Dalbergia rubiginosa
Euphorbia kansui
Foeniculum vulgare
Illicium verum
Mappia nimmoniana
Mesembryanthemum tortuosum
Satureja atropatana

Cross-Links

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PubChem 12387012
NPASS NPC209705
LOTUS LTS0058041
wikiData Q105250512