Tetrahydrolavandulol

Details

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Internal ID 2d874cd3-1861-4a21-a027-5c26aea21c94
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 5-methyl-2-propan-2-ylhexan-1-ol
SMILES (Canonical) CC(C)CCC(CO)C(C)C
SMILES (Isomeric) CC(C)CCC(CO)C(C)C
InChI InChI=1S/C10H22O/c1-8(2)5-6-10(7-11)9(3)4/h8-11H,5-7H2,1-4H3
InChI Key SFIQHFBITUEIBP-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C10H22O
Molecular Weight 158.28 g/mol
Exact Mass 158.167065321 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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2051-33-4
2-Isopropyl-5-methylhexan-1-ol
1-Hexanol, 5-methyl-2-(1-methylethyl)-
5-methyl-2-propan-2-ylhexan-1-ol
2-Isopropyl-5-methylhexanol
EINECS 218-119-3
5-methyl-2-(1-methylethyl)-hexan-1-ol
NSC65622
NCIOpen2_000231
SCHEMBL671825
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Tetrahydrolavandulol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9825 98.25%
Caco-2 + 0.7635 76.35%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.6154 61.54%
OATP2B1 inhibitior - 0.8433 84.33%
OATP1B1 inhibitior + 0.9633 96.33%
OATP1B3 inhibitior + 0.9358 93.58%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9651 96.51%
P-glycoprotein inhibitior - 0.9700 97.00%
P-glycoprotein substrate - 0.8994 89.94%
CYP3A4 substrate - 0.6995 69.95%
CYP2C9 substrate - 0.8468 84.68%
CYP2D6 substrate - 0.7359 73.59%
CYP3A4 inhibition - 0.9319 93.19%
CYP2C9 inhibition - 0.8673 86.73%
CYP2C19 inhibition - 0.9088 90.88%
CYP2D6 inhibition - 0.9366 93.66%
CYP1A2 inhibition - 0.8154 81.54%
CYP2C8 inhibition - 0.9964 99.64%
CYP inhibitory promiscuity - 0.8974 89.74%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6759 67.59%
Eye corrosion + 0.8846 88.46%
Eye irritation + 0.9791 97.91%
Skin irritation + 0.6069 60.69%
Skin corrosion - 0.9097 90.97%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5151 51.51%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5221 52.21%
skin sensitisation + 0.9148 91.48%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.9531 95.31%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6529 65.29%
Acute Oral Toxicity (c) III 0.7582 75.82%
Estrogen receptor binding - 0.9104 91.04%
Androgen receptor binding - 0.8782 87.82%
Thyroid receptor binding - 0.7872 78.72%
Glucocorticoid receptor binding - 0.8730 87.30%
Aromatase binding - 0.8974 89.74%
PPAR gamma - 0.9428 94.28%
Honey bee toxicity - 0.9664 96.64%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.7612 76.12%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 92.25% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.91% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.97% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Persicaria bistorta

Cross-Links

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PubChem 96291
NPASS NPC126509
LOTUS LTS0178604
wikiData Q105251776