3,4,5-Trihydroxy-6-(hydroxymethyl)piperidine-2-sulfonic acid

Details

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Internal ID 4e1d19cd-fa06-4807-9815-cc7709f35d49
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 3,4,5-trihydroxy-6-(hydroxymethyl)piperidine-2-sulfonic acid
SMILES (Canonical) C(C1C(C(C(C(N1)S(=O)(=O)O)O)O)O)O
SMILES (Isomeric) C(C1C(C(C(C(N1)S(=O)(=O)O)O)O)O)O
InChI InChI=1S/C6H13NO7S/c8-1-2-3(9)4(10)5(11)6(7-2)15(12,13)14/h2-11H,1H2,(H,12,13,14)
InChI Key PLICPKOWHZITQE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H13NO7S
Molecular Weight 243.24 g/mol
Exact Mass 243.04127293 g/mol
Topological Polar Surface Area (TPSA) 156.00 Ų
XlogP -5.00
Atomic LogP (AlogP) -3.75
H-Bond Acceptor 7
H-Bond Donor 6
Rotatable Bonds 2

Synonyms

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91384-36-0
3,4,5-Trihydroxy-6-(hydroxymethyl)piperidine-2-sulfonic acid
DTXSID60559266
PD026968
FT-0673026

2D Structure

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2D Structure of 3,4,5-Trihydroxy-6-(hydroxymethyl)piperidine-2-sulfonic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7807 78.07%
Caco-2 - 0.9671 96.71%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.4277 42.77%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.9611 96.11%
OATP1B3 inhibitior + 0.9397 93.97%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9834 98.34%
P-glycoprotein inhibitior - 0.9569 95.69%
P-glycoprotein substrate - 0.9252 92.52%
CYP3A4 substrate - 0.6380 63.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7958 79.58%
CYP3A4 inhibition - 0.9698 96.98%
CYP2C9 inhibition - 0.8310 83.10%
CYP2C19 inhibition - 0.8007 80.07%
CYP2D6 inhibition - 0.8951 89.51%
CYP1A2 inhibition - 0.7532 75.32%
CYP2C8 inhibition - 0.9565 95.65%
CYP inhibitory promiscuity - 0.9842 98.42%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.5748 57.48%
Carcinogenicity (trinary) Non-required 0.6486 64.86%
Eye corrosion - 0.9515 95.15%
Eye irritation - 0.9857 98.57%
Skin irritation - 0.7667 76.67%
Skin corrosion - 0.8508 85.08%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5382 53.82%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.6410 64.10%
skin sensitisation - 0.8366 83.66%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5127 51.27%
Acute Oral Toxicity (c) III 0.5617 56.17%
Estrogen receptor binding - 0.7196 71.96%
Androgen receptor binding - 0.7431 74.31%
Thyroid receptor binding - 0.6453 64.53%
Glucocorticoid receptor binding - 0.6632 66.32%
Aromatase binding - 0.8159 81.59%
PPAR gamma - 0.7514 75.14%
Honey bee toxicity - 0.5663 56.63%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.8063 80.63%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.96% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.04% 96.09%
CHEMBL255 P29275 Adenosine A2b receptor 88.99% 98.59%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.40% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.69% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 80.79% 95.93%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 14351686
LOTUS LTS0151059
wikiData Q82441928