L-RHAMNOSE
General Information
| Mainterm | L-RHAMNOSE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 3615-41-6 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 19233 |
| IUPAC Name | (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal |
| 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 |
| Canonical SMILES | CC(C(C(C(C=O)O)O)O)O |
| Molecular Formula | C6H12O5 |
| Wikipedia | rhamnose |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 164.157 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Complexity | 126.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g O A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A G g A A C A A A C B S g g A I C A A A A A g A I A A g Q g A I A A A A A A A A A A A F A A A A B E B Y A A A A A Q A A F I A A B A A H K D A B A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = = |
| Topological Polar Surface Area | 98.0 |
| Monoisotopic Mass | 164.068 |
| Exact Mass | 164.068 |
| XLogP3 | None |
| XLogP3-AA | -2.4 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 11 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Isotope Atom Count | 0 |
| Covalently-Bonded Unit Count | 1 |
From Pubchem
Food Additives Biosynthesis/Degradation
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.6505 |
| Human Intestinal Absorption | HIA+ | 0.9040 |
| Caco-2 Permeability | Caco2- | 0.8361 |
| P-glycoprotein Substrate | Non-substrate | 0.6823 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9712 |
| Non-inhibitor | 0.9665 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9588 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6942 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8163 |
| CYP450 2D6 Substrate | Non-substrate | 0.9111 |
| CYP450 3A4 Substrate | Non-substrate | 0.7357 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8235 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8432 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9503 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9466 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8437 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9379 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9882 |
| Non-inhibitor | 0.9677 | |
| AMES Toxicity | Non AMES toxic | 0.8425 |
| Carcinogens | Non-carcinogens | 0.5951 |
| Fish Toxicity | Low FHMT | 0.6846 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.5404 |
| Honey Bee Toxicity | High HBT | 0.6906 |
| Biodegradation | Ready biodegradable | 0.8253 |
| Acute Oral Toxicity | III | 0.8477 |
| Carcinogenicity (Three-class) | Non-required | 0.7552 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | 0.9352 | LogS |
| Caco-2 Permeability | -0.1622 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.3420 | LD50, mol/kg |
| Fish Toxicity | 2.7393 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -1.2070 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbohydrates and carbohydrate conjugates |
| Intermediate Tree Nodes | Monosaccharides |
| Direct Parent | Hexoses |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Hexose monosaccharide - Medium-chain aldehyde - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity. |
From ClassyFire
Targets
- General Function:
- Manganese ion binding
- Gene Name:
- rhaA
- Uniprot ID:
- P32170
- Molecular Weight:
- 47198.95 Da
From T3DB