L-Monomenthyl glutarate
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
Chemical name | L-Monomenthyl glutarate |
CAS number | 220621-22-7 |
Flavouring type | substances |
FL No. | 09.929 |
Mixture | No |
Purity of the named substance at least 95% unless otherwise specified | |
Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF2D Structure | |
CID | 24752885 |
IUPAC Name | 5-[(1R,2S,5R)-5-methyl-2-propan-2-ylcyclohexyl]oxy-5-oxopentanoic acid |
InChI | InChI=1S/C15H26O4/c1-10(2)12-8-7-11(3)9-13(12)19-15(18)6-4-5-14(16)17/h10-13H,4-9H2,1-3H3,(H,16,17)/t11-,12+,13-/m1/s1 |
InChI Key | CTMTYSVTTGVYAW-FRRDWIJNSA-N |
Canonical SMILES | CC1CCC(C(C1)OC(=O)CCCC(=O)O)C(C)C |
Molecular Formula | C15H26O4 |
Wikipedia | (-)-monomenthyl glutarate |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 270.369 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 7 |
Complexity | 311.0 |
CACTVS Substructure Key Fingerprint | A A A D c e B w 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 w A A A A A A A A A A A A A A A A G g A A C A A A D R S g g A I C C A A A B g A I A A C Q C A A A A A A A A A A A A A E A A A A A A B I A A A A C Q A A E A A A A A A G I 5 v g O g A A A A A A A A A C A A A I A A B A A A A A A A A A A A A = = |
Topological Polar Surface Area | 63.6 |
Monoisotopic Mass | 270.183 |
Exact Mass | 270.183 |
XLogP3 | None |
XLogP3-AA | 3.4 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 19 |
Defined Atom Stereocenter Count | 3 |
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
ADMET Predicted Profile --- Classification
Model | Result | Probability |
---|---|---|
Absorption | ||
Blood-Brain Barrier | BBB+ | 0.8377 |
Human Intestinal Absorption | HIA+ | 0.9096 |
Caco-2 Permeability | Caco2+ | 0.5328 |
P-glycoprotein Substrate | Substrate | 0.5197 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.7680 |
Inhibitor | 0.6108 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8876 |
Distribution | ||
Subcellular localization | Mitochondria | 0.9344 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.7939 |
CYP450 2D6 Substrate | Non-substrate | 0.8971 |
CYP450 3A4 Substrate | Substrate | 0.6115 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.9290 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.8502 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9236 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.9189 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.8008 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9757 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9201 |
Non-inhibitor | 0.8657 | |
AMES Toxicity | Non AMES toxic | 0.8609 |
Carcinogens | Non-carcinogens | 0.9054 |
Fish Toxicity | High FHMT | 0.9845 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9973 |
Honey Bee Toxicity | High HBT | 0.7591 |
Biodegradation | Not ready biodegradable | 0.5762 |
Acute Oral Toxicity | III | 0.6976 |
Carcinogenicity (Three-class) | Non-required | 0.7798 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -4.1101 | LogS |
Caco-2 Permeability | 0.7804 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.2806 | LD50, mol/kg |
Fish Toxicity | 1.0782 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 1.3167 | pIGC50, ug/L |
From admetSAR