(2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

Details

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Internal ID 998b8b12-a5e0-4572-8db4-fbfeed70df75
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name (2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal
SMILES (Canonical) C(C(C(C(C(C=O)O)O)O)O)O
SMILES (Isomeric) C([C@H]([C@H]([C@H]([C@H](C=O)O)O)O)O)O
InChI InChI=1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4+,5-,6+/m0/s1
InChI Key GZCGUPFRVQAUEE-BGPJRJDNSA-N
Popularity 996 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 -2.90
Atomic LogP (AlogP) -3.38
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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2595-97-3
(2R,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexanal
aldehydo-D-allose
dl-Allose
SV1ATP0KYY
6038-51-3
UNII-SV1ATP0KYY
EINECS 219-994-4
AOS
D-allose (OK)
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,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4790 47.90%
Caco-2 - 0.9561 95.61%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6838 68.38%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9601 96.01%
OATP1B3 inhibitior + 0.9321 93.21%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9784 97.84%
P-glycoprotein inhibitior - 0.9782 97.82%
P-glycoprotein substrate - 0.9699 96.99%
CYP3A4 substrate - 0.7223 72.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7995 79.95%
CYP3A4 inhibition - 0.9065 90.65%
CYP2C9 inhibition - 0.9411 94.11%
CYP2C19 inhibition - 0.9420 94.20%
CYP2D6 inhibition - 0.9366 93.66%
CYP1A2 inhibition - 0.8505 85.05%
CYP2C8 inhibition - 0.9923 99.23%
CYP inhibitory promiscuity - 0.9652 96.52%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.7860 78.60%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9789 97.89%
Skin irritation - 0.7107 71.07%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6918 69.18%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.8625 86.25%
skin sensitisation - 0.9302 93.02%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.5362 53.62%
Acute Oral Toxicity (c) IV 0.6209 62.09%
Estrogen receptor binding - 0.8640 86.40%
Androgen receptor binding - 0.8579 85.79%
Thyroid receptor binding - 0.6879 68.79%
Glucocorticoid receptor binding - 0.5054 50.54%
Aromatase binding - 0.8589 85.89%
PPAR gamma - 0.9009 90.09%
Honey bee toxicity - 0.9679 96.79%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.9900 99.00%
Fish aquatic toxicity - 0.9544 95.44%

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 85.90% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.60% 96.09%
CHEMBL2581 P07339 Cathepsin D 81.71% 98.95%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.49% 98.75%

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.
Podophyllum hexandrum
Pogostemon cablin

Cross-Links

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PubChem 102288
NPASS NPC1050
LOTUS LTS0023055
wikiData Q423216