2,3,4,5-Tetrahydroxy-2-(hydroxymethyl)pentanal

Details

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Internal ID 0c71fbbb-62e2-4256-8b99-a686b4897b94
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides
IUPAC Name 2,3,4,5-tetrahydroxy-2-(hydroxymethyl)pentanal
SMILES (Canonical) C(C(C(C(CO)(C=O)O)O)O)O
SMILES (Isomeric) C(C(C(C(CO)(C=O)O)O)O)O
InChI InChI=1S/C6H12O6/c7-1-4(10)5(11)6(12,2-8)3-9/h2,4-5,7,9-12H,1,3H2
InChI Key ZGVNGXVNRCEBDS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12O6
Molecular Weight 180.16 g/mol
Exact Mass 180.06338810 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP -3.70
Atomic LogP (AlogP) -3.38
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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AKOS040747084

2D Structure

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2D Structure of 2,3,4,5-Tetrahydroxy-2-(hydroxymethyl)pentanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5145 51.45%
Caco-2 - 0.9543 95.43%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7364 73.64%
OATP2B1 inhibitior - 0.8553 85.53%
OATP1B1 inhibitior + 0.9079 90.79%
OATP1B3 inhibitior + 0.9405 94.05%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9487 94.87%
P-glycoprotein inhibitior - 0.9797 97.97%
P-glycoprotein substrate - 0.9482 94.82%
CYP3A4 substrate - 0.6493 64.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7874 78.74%
CYP3A4 inhibition - 0.9353 93.53%
CYP2C9 inhibition - 0.9022 90.22%
CYP2C19 inhibition - 0.8853 88.53%
CYP2D6 inhibition - 0.9341 93.41%
CYP1A2 inhibition - 0.8468 84.68%
CYP2C8 inhibition - 0.9783 97.83%
CYP inhibitory promiscuity - 0.9727 97.27%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.7148 71.48%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.9261 92.61%
Skin irritation - 0.8275 82.75%
Skin corrosion - 0.9831 98.31%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7254 72.54%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.9034 90.34%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.4638 46.38%
Acute Oral Toxicity (c) IV 0.5256 52.56%
Estrogen receptor binding - 0.7963 79.63%
Androgen receptor binding - 0.7714 77.14%
Thyroid receptor binding - 0.6878 68.78%
Glucocorticoid receptor binding - 0.6220 62.20%
Aromatase binding - 0.7674 76.74%
PPAR gamma - 0.8511 85.11%
Honey bee toxicity - 0.9203 92.03%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.9329 93.29%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.89% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.77% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.61% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.60% 95.56%

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.
Cnidium monnieri

Cross-Links

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PubChem 15559619
LOTUS LTS0135445
wikiData Q105375449