Neurine

Details

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Internal ID a850255f-e51a-40c2-9d9a-80c87415c91a
Taxonomy Alkaloids and derivatives
IUPAC Name ethenyl(trimethyl)azanium hydroxide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H12N.H2O/c1-5-6(2,3)4;/h5H,1H2,2-4H3;1H2/q+1;/p-1
InChI Key NIPLIJLVGZCKMP-UHFFFAOYSA-M
Popularity 341 references in papers

Physical and Chemical Properties

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Molecular Formula C5H13NO
Molecular Weight 103.16 g/mol
Exact Mass 103.099714038 g/mol
Topological Polar Surface Area (TPSA) 1.00 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.66
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Vitaloid
Neurin
trimethylvinylammonium hydroxide
Neirin
Neirine
Vinyltrimethylammonium hydroxide
N,N,N-Trimethylethenaminium hydroxide
Trimethyl vinyl ammonium hydroxide
Trimethyl(vinyl)ammonium hydroxide
Ethenaminium, N,N,N-trimethyl-, hydroxide
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Neurine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8897 88.97%
Caco-2 + 0.6600 66.00%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.4989 49.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9653 96.53%
OATP1B3 inhibitior + 0.9463 94.63%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9260 92.60%
P-glycoprotein inhibitior - 0.9843 98.43%
P-glycoprotein substrate - 0.9907 99.07%
CYP3A4 substrate - 0.7428 74.28%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7563 75.63%
CYP3A4 inhibition - 0.8719 87.19%
CYP2C9 inhibition - 0.9055 90.55%
CYP2C19 inhibition - 0.8948 89.48%
CYP2D6 inhibition - 0.9410 94.10%
CYP1A2 inhibition - 0.8683 86.83%
CYP2C8 inhibition - 0.9800 98.00%
CYP inhibitory promiscuity - 0.9371 93.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.6794 67.94%
Eye corrosion + 0.7506 75.06%
Eye irritation + 0.9902 99.02%
Skin irritation + 0.6227 62.27%
Skin corrosion - 0.5442 54.42%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7904 79.04%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5731 57.31%
skin sensitisation - 0.7532 75.32%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.5178 51.78%
Nephrotoxicity + 0.6965 69.65%
Acute Oral Toxicity (c) III 0.7075 70.75%
Estrogen receptor binding - 0.9044 90.44%
Androgen receptor binding - 0.9483 94.83%
Thyroid receptor binding - 0.8646 86.46%
Glucocorticoid receptor binding - 0.8076 80.76%
Aromatase binding - 0.8403 84.03%
PPAR gamma - 0.8393 83.93%
Honey bee toxicity - 0.8116 81.16%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.7237 72.37%

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
No predicted targets yet!

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.
Cannabis sativa

Cross-Links

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PubChem 10042
NPASS NPC132043