D-SORBITOL
Relevant Data
Food Additives Approved by WHO:
General Information
| Mainterm | D-SORBITOL |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 50-70-4 |
| Regnum |
175.300 175.320 176.180 176.210 177.1390 177.2420 182.90 101.9 100.130 101.80 184.1835 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 5780 |
| IUPAC Name | (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol |
| InChI | InChI=1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5-,6-/m1/s1 |
| InChI Key | FBPFZTCFMRRESA-JGWLITMVSA-N |
| Canonical SMILES | C(C(C(C(C(CO)O)O)O)O)O |
| Molecular Formula | C6H14O6 |
| Wikipedia | sorbitol |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 182.172 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 5 |
| Complexity | 105.0 |
| 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 A A A A A A g 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 B E A I A A A A A Q A A F A A A B A A H A Y A Q 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 | 121.0 |
| Monoisotopic Mass | 182.079 |
| Exact Mass | 182.079 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 12 |
| 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- | 0.5997 |
| Human Intestinal Absorption | HIA+ | 0.6525 |
| Caco-2 Permeability | Caco2- | 0.8958 |
| P-glycoprotein Substrate | Non-substrate | 0.6620 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9535 |
| Non-inhibitor | 0.9551 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9252 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5618 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8706 |
| CYP450 2D6 Substrate | Non-substrate | 0.8780 |
| CYP450 3A4 Substrate | Non-substrate | 0.7431 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.8240 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9419 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9412 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9232 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9402 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9580 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9709 |
| Non-inhibitor | 0.9329 | |
| AMES Toxicity | Non AMES toxic | 0.9132 |
| Carcinogens | Non-carcinogens | 0.7823 |
| Fish Toxicity | Low FHMT | 0.9260 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.9924 |
| Honey Bee Toxicity | High HBT | 0.6756 |
| Biodegradation | Ready biodegradable | 0.8595 |
| Acute Oral Toxicity | IV | 0.6451 |
| Carcinogenicity (Three-class) | Non-required | 0.6932 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | 1.0329 | LogS |
| Caco-2 Permeability | -0.3908 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.1260 | LD50, mol/kg |
| Fish Toxicity | 3.1559 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -1.9267 | 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 | Not available |
| Direct Parent | Sugar alcohols |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Sugar alcohol - Monosaccharide - Secondary alcohol - Polyol - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as sugar alcohols. These are hydrogenated forms of carbohydrate in which the carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group. |
From ClassyFire
Targets
- General Function:
- Xylose isomerase activity
- Specific Function:
- Involved in D-xylose catabolism.
- Gene Name:
- xylA
- Uniprot ID:
- P24300
- Molecular Weight:
- 43226.915 Da
- General Function:
- Xylose isomerase activity
- Gene Name:
- xylA
- Uniprot ID:
- P12851
- Molecular Weight:
- 43498.425 Da
- General Function:
- Xylose isomerase activity
- Gene Name:
- xylA
- Uniprot ID:
- P12070
- Molecular Weight:
- 43291.15 Da
- General Function:
- Metal ion binding
- Specific Function:
- Involved in the glycolate utilization. Catalyzes the condensation and subsequent hydrolysis of acetyl-coenzyme A (acetyl-CoA) and glyoxylate to form malate and CoA.
- Gene Name:
- glcB
- Uniprot ID:
- P37330
- Molecular Weight:
- 80487.88 Da
From T3DB