(S)-6-Amino-2-(dimethylamino)-2-methylhexanoic acid

Details

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Internal ID 33d6adf1-4c76-4cb6-90a4-88038e04b6b7
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > D-alpha-amino acids
IUPAC Name (2S)-6-amino-2-(dimethylamino)-2-methylhexanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H20N2O2/c1-9(8(12)13,11(2)3)6-4-5-7-10/h4-7,10H2,1-3H3,(H,12,13)/t9-/m0/s1
InChI Key YOZNFSJEWZFKCV-VIFPVBQESA-N
Popularity 466 references in papers

Physical and Chemical Properties

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Molecular Formula C9H20N2O2
Molecular Weight 188.27 g/mol
Exact Mass 188.152477885 g/mol
Topological Polar Surface Area (TPSA) 66.60 Ų
XlogP -2.10
Atomic LogP (AlogP) 0.52
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (S)-6-Amino-2-(dimethylamino)-2-methylhexanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8275 82.75%
Caco-2 + 0.8363 83.63%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.8293 82.93%
OATP2B1 inhibitior - 0.8475 84.75%
OATP1B1 inhibitior + 0.9455 94.55%
OATP1B3 inhibitior + 0.9409 94.09%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9411 94.11%
P-glycoprotein inhibitior - 0.9904 99.04%
P-glycoprotein substrate - 0.8077 80.77%
CYP3A4 substrate - 0.5984 59.84%
CYP2C9 substrate - 0.5888 58.88%
CYP2D6 substrate - 0.7263 72.63%
CYP3A4 inhibition - 0.9095 90.95%
CYP2C9 inhibition - 0.9197 91.97%
CYP2C19 inhibition - 0.9400 94.00%
CYP2D6 inhibition - 0.8959 89.59%
CYP1A2 inhibition - 0.9206 92.06%
CYP2C8 inhibition - 0.9735 97.35%
CYP inhibitory promiscuity - 0.9925 99.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.6095 60.95%
Eye corrosion - 0.7970 79.70%
Eye irritation - 0.7364 73.64%
Skin irritation - 0.6543 65.43%
Skin corrosion - 0.5822 58.22%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7004 70.04%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.6954 69.54%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.6655 66.55%
Acute Oral Toxicity (c) III 0.6800 68.00%
Estrogen receptor binding - 0.9255 92.55%
Androgen receptor binding - 0.7502 75.02%
Thyroid receptor binding - 0.7471 74.71%
Glucocorticoid receptor binding - 0.7861 78.61%
Aromatase binding - 0.8264 82.64%
PPAR gamma - 0.7986 79.86%
Honey bee toxicity - 0.9646 96.46%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.7162 71.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.68% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.42% 99.17%
CHEMBL2581 P07339 Cathepsin D 89.15% 98.95%
CHEMBL4581 P52732 Kinesin-like protein 1 86.15% 93.18%
CHEMBL3401 O75469 Pregnane X receptor 82.68% 94.73%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.08% 100.00%
CHEMBL2885 P07451 Carbonic anhydrase III 80.97% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.61% 97.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.53% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 22815233
LOTUS LTS0273252
wikiData Q105351605