Methylazoxymethanol

Details

Top
Internal ID 9da3b5a2-c05f-420e-aaf8-740c0bb419aa
Taxonomy Organic 1,3-dipolar compounds > Allyl-type 1,3-dipolar organic compounds > Azoxy compounds
IUPAC Name (Z)-hydroxymethylimino-methyl-oxidoazanium
SMILES (Canonical) C[N+](=NCO)[O-]
SMILES (Isomeric) C/[N+](=N/CO)/[O-]
InChI InChI=1S/C2H6N2O2/c1-4(6)3-2-5/h5H,2H2,1H3/b4-3-
InChI Key BJNBRIBHKLJMAG-ARJAWSKDSA-N
Popularity 275 references in papers

Physical and Chemical Properties

Top
Molecular Formula C2H6N2O2
Molecular Weight 90.08 g/mol
Exact Mass 90.042927438 g/mol
Topological Polar Surface Area (TPSA) 61.30 Ų
XlogP -0.80
Atomic LogP (AlogP) -0.47
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
590-96-5
Methanol, (methyl-ONN-azoxy)-
UNII-JGG19N3YDQ
JGG19N3YDQ
(methyl-ONN-azoxy)methanol
CCRIS 1113
HSDB 3509
BRN 1921057
1-Hydroxymethyl-2-methylditmide-2-oxide
MAM
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Methylazoxymethanol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8495 84.95%
Caco-2 - 0.5885 58.85%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.5736 57.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9265 92.65%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9370 93.70%
P-glycoprotein inhibitior - 0.9791 97.91%
P-glycoprotein substrate - 0.9853 98.53%
CYP3A4 substrate - 0.7120 71.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8418 84.18%
CYP3A4 inhibition - 0.9826 98.26%
CYP2C9 inhibition - 0.8095 80.95%
CYP2C19 inhibition - 0.7749 77.49%
CYP2D6 inhibition - 0.9010 90.10%
CYP1A2 inhibition - 0.7095 70.95%
CYP2C8 inhibition - 0.9879 98.79%
CYP inhibitory promiscuity - 0.9860 98.60%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) + 0.6062 60.62%
Carcinogenicity (trinary) Danger 0.4978 49.78%
Eye corrosion - 0.9103 91.03%
Eye irritation + 0.8375 83.75%
Skin irritation - 0.5638 56.38%
Skin corrosion - 0.8792 87.92%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7649 76.49%
Micronuclear + 0.9000 90.00%
Hepatotoxicity + 0.6178 61.78%
skin sensitisation - 0.8028 80.28%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5975 59.75%
Acute Oral Toxicity (c) III 0.5974 59.74%
Estrogen receptor binding - 0.9304 93.04%
Androgen receptor binding - 0.9320 93.20%
Thyroid receptor binding - 0.8419 84.19%
Glucocorticoid receptor binding - 0.8850 88.50%
Aromatase binding - 0.9367 93.67%
PPAR gamma - 0.9181 91.81%
Honey bee toxicity - 0.9173 91.73%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.9567 95.67%

Targets

Top

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 90.72% 96.09%
CHEMBL2581 P07339 Cathepsin D 81.52% 98.95%

Plants that contains it

Top
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.
Cycas revoluta
Nelumbo nucifera

Cross-Links

Top
PubChem 6433205
NPASS NPC239480