TETRAHYDROLINALOOL
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
Mainterm | TETRAHYDROLINALOOL |
Doc Type | ASP |
CAS Reg.No.(or other ID) | 78-69-3 |
Regnum |
172.515 |
From www.fda.gov
Computed Descriptors
Download SDF2D Structure | |
CID | 6548 |
IUPAC Name | 3,7-dimethyloctan-3-ol |
InChI | InChI=1S/C10H22O/c1-5-10(4,11)8-6-7-9(2)3/h9,11H,5-8H2,1-4H3 |
InChI Key | DLHQZZUEERVIGQ-UHFFFAOYSA-N |
Canonical SMILES | CCC(C)(CCCC(C)C)O |
Molecular Formula | C10H22O |
Wikipedia | tetrahydrolinalool |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 158.285 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 5 |
Complexity | 99.0 |
CACTVS Substructure Key Fingerprint | A A A D c e B w I 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 D U S A g A A C 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 A A A I A A A A A Q A A E A A A A A A G A w N A 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 | 20.2 |
Monoisotopic Mass | 158.167 |
Exact Mass | 158.167 |
XLogP3 | None |
XLogP3-AA | 3.3 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 11 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 1 |
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+ | 0.9837 |
Human Intestinal Absorption | HIA+ | 0.9905 |
Caco-2 Permeability | Caco2+ | 0.7710 |
P-glycoprotein Substrate | Substrate | 0.5082 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.8605 |
Non-inhibitor | 0.6131 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.9209 |
Distribution | ||
Subcellular localization | Mitochondria | 0.4601 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8234 |
CYP450 2D6 Substrate | Non-substrate | 0.8410 |
CYP450 3A4 Substrate | Substrate | 0.5176 |
CYP450 1A2 Inhibitor | Inhibitor | 0.5605 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.8007 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9341 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.8736 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9318 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8390 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9377 |
Non-inhibitor | 0.6950 | |
AMES Toxicity | Non AMES toxic | 0.9576 |
Carcinogens | Carcinogens | 0.5398 |
Fish Toxicity | High FHMT | 0.8100 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9890 |
Honey Bee Toxicity | High HBT | 0.7654 |
Biodegradation | Not ready biodegradable | 0.7243 |
Acute Oral Toxicity | III | 0.8214 |
Carcinogenicity (Three-class) | Non-required | 0.7272 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -2.2685 | LogS |
Caco-2 Permeability | 1.3423 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 1.5321 | LD50, mol/kg |
Fish Toxicity | 0.9764 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.4653 | pIGC50, ug/L |
From admetSAR
Toxicity Profile
Route of Exposure | |
---|---|
Mechanism of Toxicity | |
Metabolism | |
Toxicity Values | |
Lethal Dose | |
Carcinogenicity (IARC Classification) | No indication of carcinogenicity to humans (not listed by IARC). |
Minimum Risk Level | |
Health Effects | |
Treatment | |
Reference |
|
From T3DB
Taxonomic Classification
Kingdom | Organic compounds |
---|---|
Superclass | Organic oxygen compounds |
Class | Organooxygen compounds |
Subclass | Alcohols and polyols |
Intermediate Tree Nodes | Not available |
Direct Parent | Tertiary alcohols |
Alternative Parents | |
Molecular Framework | Aliphatic acyclic compounds |
Substituents | Tertiary alcohol - Hydrocarbon derivative - Aliphatic acyclic compound |
Description | This compound belongs to the class of organic compounds known as tertiary alcohols. These are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). |
From ClassyFire
Targets
- General Function:
- Zinc ion binding
- Specific Function:
- Nuclear hormone receptor. The steroid hormones and their receptors are involved in the regulation of eukaryotic gene expression and affect cellular proliferation and differentiation in target tissues. Ligand-dependent nuclear transactivation involves either direct homodimer binding to a palindromic estrogen response element (ERE) sequence or association with other DNA-binding transcription factors, such as AP-1/c-Jun, c-Fos, ATF-2, Sp1 and Sp3, to mediate ERE-independent signaling. Ligand binding induces a conformational change allowing subsequent or combinatorial association with multiprotein coactivator complexes through LXXLL motifs of their respective components. Mutual transrepression occurs between the estrogen receptor (ER) and NF-kappa-B in a cell-type specific manner. Decreases NF-kappa-B DNA-binding activity and inhibits NF-kappa-B-mediated transcription from the IL6 promoter and displace RELA/p65 and associated coregulators from the promoter. Recruited to the NF-kappa-B response element of the CCL2 and IL8 promoters and can displace CREBBP. Present with NF-kappa-B components RELA/p65 and NFKB1/p50 on ERE sequences. Can also act synergistically with NF-kappa-B to activate transcription involving respective recruitment adjacent response elements; the function involves CREBBP. Can activate the transcriptional activity of TFF1. Also mediates membrane-initiated estrogen signaling involving various kinase cascades. Isoform 3 is involved in activation of NOS3 and endothelial nitric oxide production. Isoforms lacking one or several functional domains are thought to modulate transcriptional activity by competitive ligand or DNA binding and/or heterodimerization with the full length receptor. Essential for MTA1-mediated transcriptional regulation of BRCA1 and BCAS3. Isoform 3 can bind to ERE and inhibit isoform 1.
- Gene Name:
- ESR1
- Uniprot ID:
- P03372
- Molecular Weight:
- 66215.45 Da
References
- Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]
From T3DB