(1S,2R,3R)-3-(2-hydroxyethyl)-2-(hydroxymethyl)-1-methylcyclopentan-1-ol

Details

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Internal ID 8e4e3e25-0ecd-4e1f-89ed-94eea1738fdf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Iridoids and derivatives
IUPAC Name (1S,2R,3R)-3-(2-hydroxyethyl)-2-(hydroxymethyl)-1-methylcyclopentan-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H18O3/c1-9(12)4-2-7(3-5-10)8(9)6-11/h7-8,10-12H,2-6H2,1H3/t7-,8+,9+/m1/s1
InChI Key MFNWXGSFLDKZTF-VGMNWLOBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18O3
Molecular Weight 174.24 g/mol
Exact Mass 174.125594432 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.14
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,2R,3R)-3-(2-hydroxyethyl)-2-(hydroxymethyl)-1-methylcyclopentan-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9245 92.45%
Caco-2 + 0.4934 49.34%
Blood Brain Barrier + 0.5635 56.35%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5070 50.70%
OATP2B1 inhibitior - 0.8453 84.53%
OATP1B1 inhibitior + 0.9278 92.78%
OATP1B3 inhibitior + 0.9489 94.89%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7893 78.93%
BSEP inhibitior - 0.9353 93.53%
P-glycoprotein inhibitior - 0.9807 98.07%
P-glycoprotein substrate - 0.9159 91.59%
CYP3A4 substrate - 0.5275 52.75%
CYP2C9 substrate - 0.6538 65.38%
CYP2D6 substrate - 0.7704 77.04%
CYP3A4 inhibition - 0.9583 95.83%
CYP2C9 inhibition - 0.7855 78.55%
CYP2C19 inhibition - 0.8796 87.96%
CYP2D6 inhibition - 0.9370 93.70%
CYP1A2 inhibition - 0.8115 81.15%
CYP2C8 inhibition - 0.9057 90.57%
CYP inhibitory promiscuity - 0.9574 95.74%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6448 64.48%
Eye corrosion - 0.9775 97.75%
Eye irritation + 0.8317 83.17%
Skin irritation - 0.6490 64.90%
Skin corrosion - 0.9575 95.75%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6120 61.20%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5522 55.22%
skin sensitisation - 0.8109 81.09%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5901 59.01%
Acute Oral Toxicity (c) III 0.6779 67.79%
Estrogen receptor binding - 0.8222 82.22%
Androgen receptor binding - 0.6322 63.22%
Thyroid receptor binding - 0.7732 77.32%
Glucocorticoid receptor binding - 0.7977 79.77%
Aromatase binding - 0.9001 90.01%
PPAR gamma - 0.8935 89.35%
Honey bee toxicity - 0.9579 95.79%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.4874 48.74%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.93% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.29% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 93.37% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.05% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.68% 97.09%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.52% 95.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.98% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.83% 96.61%
CHEMBL233 P35372 Mu opioid receptor 82.93% 97.93%
CHEMBL1937 Q92769 Histone deacetylase 2 82.09% 94.75%
CHEMBL2996 Q05655 Protein kinase C delta 80.77% 97.79%

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.
Pedicularis densispica

Cross-Links

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PubChem 53483796
LOTUS LTS0080930
wikiData Q105162878