ALKYL(C9-11) BENZOATE, BRANCHED
General Information
| Mainterm | ALKYL(C9-11) BENZOATE, BRANCHED |
| CAS Reg.No.(or other ID) | 131298-44-7 |
| Regnum |
175.105 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 3078322 |
| IUPAC Name | 8-methylnonyl benzoate |
| InChI | InChI=1S/C17H26O2/c1-15(2)11-7-4-3-5-10-14-19-17(18)16-12-8-6-9-13-16/h6,8-9,12-13,15H,3-5,7,10-11,14H2,1-2H3 |
| InChI Key | HNDYULRADYGBDU-UHFFFAOYSA-N |
| Canonical SMILES | CC(C)CCCCCCCOC(=O)C1=CC=CC=C1 |
| Molecular Formula | C17H26O2 |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 262.393 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 10 |
| Complexity | 229.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B 4 M 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 B A A A A G g A A A A A A D Q C g m A I y C I A A B A C I A i D S C A A C A A A k A A A I i A E A C M g I J j K A N R i C M Q A k w A E I q Y e I y O C 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 = = |
| Topological Polar Surface Area | 26.3 |
| Monoisotopic Mass | 262.193 |
| Exact Mass | 262.193 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 19 |
| Defined Atom Stereocenter Count | 0 |
| 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+ | 0.9804 |
| Human Intestinal Absorption | HIA+ | 0.9956 |
| Caco-2 Permeability | Caco2+ | 0.8161 |
| P-glycoprotein Substrate | Non-substrate | 0.6277 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9342 |
| Non-inhibitor | 0.8965 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7648 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7259 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8353 |
| CYP450 2D6 Substrate | Non-substrate | 0.8732 |
| CYP450 3A4 Substrate | Non-substrate | 0.5649 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5644 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8954 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9025 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8903 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9488 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8434 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9159 |
| Non-inhibitor | 0.8203 | |
| AMES Toxicity | Non AMES toxic | 0.9437 |
| Carcinogens | Non-carcinogens | 0.7017 |
| Fish Toxicity | High FHMT | 0.9820 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9998 |
| Honey Bee Toxicity | High HBT | 0.6662 |
| Biodegradation | Ready biodegradable | 0.8126 |
| Acute Oral Toxicity | III | 0.7081 |
| Carcinogenicity (Three-class) | Non-required | 0.5984 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -4.9108 | LogS |
| Caco-2 Permeability | 1.5659 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5977 | LD50, mol/kg |
| Fish Toxicity | 0.0963 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 1.7714 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzoic acid esters |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Benzoate ester - Benzoyl - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. |
From ClassyFire