(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal

Details

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Internal ID d1c53cb2-babe-4a7d-8136-e4d36aa86400
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal
SMILES (Canonical) CC(C(C(C(C=O)O)O)O)O
SMILES (Isomeric) C[C@@H]([C@@H]([C@H]([C@H](C=O)O)O)O)O
InChI InChI=1S/C6H12O5/c1-3(8)5(10)6(11)4(9)2-7/h2-6,8-11H,1H3/t3-,4-,5-,6-/m0/s1
InChI Key PNNNRSAQSRJVSB-BXKVDMCESA-N
Popularity 14,854 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12O5
Molecular Weight 164.16 g/mol
Exact Mass 164.06847348 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP -2.40
Atomic LogP (AlogP) -2.35
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal
aldehydo-L-rhamnose
L-Mannose, 6-deoxy-
Isodulcitol
Rhamnose, L-
Locaose
Rhamnose (VAN)
Mannomethylose, L-
FEMA No. 3730
UNII-QN34XC755A
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7577 75.77%
Caco-2 - 0.9214 92.14%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6942 69.42%
OATP2B1 inhibitior - 0.8616 86.16%
OATP1B1 inhibitior + 0.9485 94.85%
OATP1B3 inhibitior + 0.9753 97.53%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9767 97.67%
P-glycoprotein inhibitior - 0.9773 97.73%
P-glycoprotein substrate - 0.9796 97.96%
CYP3A4 substrate - 0.7253 72.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7979 79.79%
CYP3A4 inhibition - 0.8437 84.37%
CYP2C9 inhibition - 0.8432 84.32%
CYP2C19 inhibition - 0.9466 94.66%
CYP2D6 inhibition - 0.9503 95.03%
CYP1A2 inhibition - 0.8235 82.35%
CYP2C8 inhibition - 0.9950 99.50%
CYP inhibitory promiscuity - 0.9379 93.79%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.6023 60.23%
Carcinogenicity (trinary) Non-required 0.7552 75.52%
Eye corrosion - 0.8420 84.20%
Eye irritation - 0.9866 98.66%
Skin irritation + 0.5812 58.12%
Skin corrosion - 0.5541 55.41%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7794 77.94%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9265 92.65%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.6402 64.02%
Acute Oral Toxicity (c) III 0.8477 84.77%
Estrogen receptor binding - 0.8095 80.95%
Androgen receptor binding - 0.9159 91.59%
Thyroid receptor binding - 0.6618 66.18%
Glucocorticoid receptor binding - 0.8049 80.49%
Aromatase binding - 0.8597 85.97%
PPAR gamma - 0.9150 91.50%
Honey bee toxicity - 0.9206 92.06%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.9800 98.00%
Fish aquatic toxicity - 0.8156 81.56%

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
CHEMBL3492 P49721 Proteasome Macropain subunit 87.69% 90.24%
CHEMBL2581 P07339 Cathepsin D 86.93% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.74% 96.09%
CHEMBL4208 P20618 Proteasome component C5 83.05% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.36% 95.56%

Cross-Links

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PubChem 19233
NPASS NPC287707
LOTUS LTS0247365
wikiData Q414109