(5-Methylpyrazin-2-yl)methanol

Details

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Internal ID 57587259-e813-4fed-8bb4-d1c87b4833de
Taxonomy Organoheterocyclic compounds > Diazines > Pyrazines
IUPAC Name (5-methylpyrazin-2-yl)methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H8N2O/c1-5-2-8-6(4-9)3-7-5/h2-3,9H,4H2,1H3
InChI Key QYANNJBVADZUDN-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8N2O
Molecular Weight 124.14 g/mol
Exact Mass 124.063662883 g/mol
Topological Polar Surface Area (TPSA) 46.00 Ų
XlogP -0.70
Atomic LogP (AlogP) 0.28
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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RefChem:404135
865-323-9
61892-95-3
5-Methyl-2-pyrazinemethanol
5-Methyl-2-pyrazinylmethanol
MFCD11044903
2-pyrazinemethanol, 5-methyl-
orb3029655
SCHEMBL2517213
(5-Methyl-2-pyrazinyl)methanol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (5-Methylpyrazin-2-yl)methanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 + 0.5332 53.32%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7513 75.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9539 95.39%
OATP1B3 inhibitior + 0.9536 95.36%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8568 85.68%
P-glycoprotein inhibitior - 0.9816 98.16%
P-glycoprotein substrate - 0.9549 95.49%
CYP3A4 substrate - 0.7031 70.31%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7917 79.17%
CYP3A4 inhibition - 0.9448 94.48%
CYP2C9 inhibition - 0.9634 96.34%
CYP2C19 inhibition - 0.9418 94.18%
CYP2D6 inhibition - 0.9682 96.82%
CYP1A2 inhibition - 0.6626 66.26%
CYP2C8 inhibition - 0.9632 96.32%
CYP inhibitory promiscuity - 0.9707 97.07%
UGT catelyzed - 0.5841 58.41%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.7376 73.76%
Eye corrosion - 0.9481 94.81%
Eye irritation + 0.9788 97.88%
Skin irritation + 0.5783 57.83%
Skin corrosion - 0.6314 63.14%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6426 64.26%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5147 51.47%
skin sensitisation - 0.7414 74.14%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6861 68.61%
Acute Oral Toxicity (c) III 0.7922 79.22%
Estrogen receptor binding - 0.8702 87.02%
Androgen receptor binding - 0.9323 93.23%
Thyroid receptor binding - 0.8711 87.11%
Glucocorticoid receptor binding - 0.9235 92.35%
Aromatase binding - 0.8551 85.51%
PPAR gamma - 0.8682 86.82%
Honey bee toxicity - 0.9885 98.85%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.9878 98.78%

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
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 92.97% 93.10%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.68% 96.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.10% 90.24%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.69% 93.65%
CHEMBL4208 P20618 Proteasome component C5 81.11% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 80.22% 94.73%

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 580061
LOTUS LTS0168848
wikiData Q72496272