2-Azaniumyl-4-(diaminomethylideneazaniumyloxy)butanoate

Details

Top
Internal ID fa586999-f60b-4480-aac1-626f12822329
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 2-azaniumyl-4-(diaminomethylideneazaniumyloxy)butanoate
SMILES (Canonical) C(CO[NH+]=C(N)N)C(C(=O)[O-])[NH3+]
SMILES (Isomeric) C(CO[NH+]=C(N)N)C(C(=O)[O-])[NH3+]
InChI InChI=1S/C5H12N4O3/c6-3(4(10)11)1-2-12-9-5(7)8/h3H,1-2,6H2,(H,10,11)(H4,7,8,9)/p+1
InChI Key FSBIGDSBMBYOPN-UHFFFAOYSA-O
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C5H13N4O3+
Molecular Weight 177.18 g/mol
Exact Mass 177.09876529 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP -3.40
Atomic LogP (AlogP) -5.98
H-Bond Acceptor 3
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-Azaniumyl-4-(diaminomethylideneazaniumyloxy)butanoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8768 87.68%
Caco-2 - 0.8580 85.80%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7181 71.81%
OATP2B1 inhibitior - 0.8488 84.88%
OATP1B1 inhibitior + 0.9578 95.78%
OATP1B3 inhibitior + 0.9401 94.01%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9450 94.50%
P-glycoprotein inhibitior - 0.9825 98.25%
P-glycoprotein substrate - 0.8824 88.24%
CYP3A4 substrate - 0.5913 59.13%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8227 82.27%
CYP3A4 inhibition - 0.8697 86.97%
CYP2C9 inhibition - 0.8855 88.55%
CYP2C19 inhibition - 0.8705 87.05%
CYP2D6 inhibition - 0.9124 91.24%
CYP1A2 inhibition - 0.8550 85.50%
CYP2C8 inhibition - 0.9631 96.31%
CYP inhibitory promiscuity - 0.9421 94.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5123 51.23%
Eye corrosion - 0.9689 96.89%
Eye irritation - 0.8182 81.82%
Skin irritation - 0.7680 76.80%
Skin corrosion - 0.8914 89.14%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6219 62.19%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8424 84.24%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7392 73.92%
Acute Oral Toxicity (c) III 0.5165 51.65%
Estrogen receptor binding - 0.8378 83.78%
Androgen receptor binding - 0.8322 83.22%
Thyroid receptor binding - 0.8352 83.52%
Glucocorticoid receptor binding - 0.8104 81.04%
Aromatase binding - 0.8549 85.49%
PPAR gamma - 0.7205 72.05%
Honey bee toxicity - 0.8088 80.88%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.8823 88.23%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.13% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.86% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.60% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.30% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.04% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.07% 94.45%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.52% 100.00%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 80.31% 83.10%

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.
Astragalus mongholicus
Astragalus sinicus
Canavalia gladiata

Cross-Links

Top
PubChem 25243900
NPASS NPC15620