(2S,3S,4S,5R)-2-(2-hydroxyethyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol

Details

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Internal ID 424e4aec-e44f-4246-bf97-fec43a92a4c0
Taxonomy Organoheterocyclic compounds > Pyrrolidines
IUPAC Name (2S,3S,4S,5R)-2-(2-hydroxyethyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H15NO4/c9-2-1-4-6(11)7(12)5(3-10)8-4/h4-12H,1-3H2/t4-,5+,6-,7-/m0/s1
InChI Key AGFACLQFIYFFOI-VZFHVOOUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H15NO4
Molecular Weight 177.20 g/mol
Exact Mass 177.10010796 g/mol
Topological Polar Surface Area (TPSA) 93.00 Ų
XlogP -2.00
Atomic LogP (AlogP) -2.58
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,3S,4S,5R)-2-(2-hydroxyethyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7377 73.77%
Caco-2 - 0.9170 91.70%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5486 54.86%
OATP2B1 inhibitior - 0.8509 85.09%
OATP1B1 inhibitior + 0.9474 94.74%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9581 95.81%
P-glycoprotein inhibitior - 0.9807 98.07%
P-glycoprotein substrate - 0.9194 91.94%
CYP3A4 substrate - 0.6968 69.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4714 47.14%
CYP3A4 inhibition - 0.9885 98.85%
CYP2C9 inhibition - 0.9390 93.90%
CYP2C19 inhibition - 0.9583 95.83%
CYP2D6 inhibition - 0.9288 92.88%
CYP1A2 inhibition - 0.8685 86.85%
CYP2C8 inhibition - 0.9594 95.94%
CYP inhibitory promiscuity - 0.9817 98.17%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7158 71.58%
Eye corrosion - 0.9639 96.39%
Eye irritation - 0.8290 82.90%
Skin irritation - 0.7389 73.89%
Skin corrosion - 0.8423 84.23%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5204 52.04%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.5998 59.98%
skin sensitisation - 0.8937 89.37%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5761 57.61%
Acute Oral Toxicity (c) III 0.5416 54.16%
Estrogen receptor binding - 0.8946 89.46%
Androgen receptor binding - 0.7650 76.50%
Thyroid receptor binding - 0.7801 78.01%
Glucocorticoid receptor binding - 0.5815 58.15%
Aromatase binding - 0.8396 83.96%
PPAR gamma - 0.8253 82.53%
Honey bee toxicity - 0.8836 88.36%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.9923 99.23%

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 89.66% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.76% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.33% 97.25%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 84.60% 94.55%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.55% 86.92%
CHEMBL226 P30542 Adenosine A1 receptor 81.46% 95.93%

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.
Muscari armeniacum

Cross-Links

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PubChem 131170181
LOTUS LTS0085136
wikiData Q104911727