L-Rhamnulose

Details

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Internal ID 1a0f8ba3-9046-4dcd-86f3-8b913b3335f7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (3R,4S,5S)-1,3,4,5-tetrahydroxyhexan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H12O5/c1-3(8)5(10)6(11)4(9)2-7/h3,5-8,10-11H,2H2,1H3/t3-,5-,6-/m0/s1
InChI Key QZNPNKJXABGCRC-FUTKDDECSA-N
Popularity 13 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 -2.20
Atomic LogP (AlogP) -2.35
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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6-deoxy-L-fructose
14807-05-7
rhamnulose
L-Fructose, 6-deoxy-
6-deoxy-L-arabino-hex-2-ulose
(3R,4S,5S)-1,3,4,5-tetrahydroxyhexan-2-one
keto-L-rhamnulose
6-deoxy L-fructose
SCHEMBL3392724
CHEBI:17897
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of L-Rhamnulose

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4944 49.44%
Caco-2 - 0.9395 93.95%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7721 77.21%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9473 94.73%
OATP1B3 inhibitior + 0.9503 95.03%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9668 96.68%
P-glycoprotein inhibitior - 0.9728 97.28%
P-glycoprotein substrate - 0.9500 95.00%
CYP3A4 substrate - 0.7055 70.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8139 81.39%
CYP3A4 inhibition - 0.9143 91.43%
CYP2C9 inhibition - 0.9034 90.34%
CYP2C19 inhibition - 0.9375 93.75%
CYP2D6 inhibition - 0.9376 93.76%
CYP1A2 inhibition - 0.8463 84.63%
CYP2C8 inhibition - 0.9955 99.55%
CYP inhibitory promiscuity - 0.9456 94.56%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8323 83.23%
Carcinogenicity (trinary) Non-required 0.7732 77.32%
Eye corrosion - 0.9781 97.81%
Eye irritation - 0.8957 89.57%
Skin irritation - 0.7512 75.12%
Skin corrosion - 0.9390 93.90%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7774 77.74%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.5409 54.09%
skin sensitisation - 0.9524 95.24%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.8719 87.19%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.6087 60.87%
Acute Oral Toxicity (c) IV 0.6480 64.80%
Estrogen receptor binding - 0.8329 83.29%
Androgen receptor binding - 0.8525 85.25%
Thyroid receptor binding - 0.7367 73.67%
Glucocorticoid receptor binding - 0.6868 68.68%
Aromatase binding - 0.8568 85.68%
PPAR gamma - 0.7943 79.43%
Honey bee toxicity - 0.9356 93.56%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.9600 96.00%
Fish aquatic toxicity - 0.9344 93.44%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.18% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.47% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.61% 85.14%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.23% 97.29%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.14% 100.00%

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.
There are no matching plants.

Cross-Links

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PubChem 14461866
LOTUS LTS0206772
wikiData Q27102710