3-methylpurin-6-amine

Details

Top
Internal ID 481504d9-6a23-41de-8e9b-29e9fa5bef74
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > 6-aminopurines
IUPAC Name 3-methylpurin-6-amine
SMILES (Canonical) CN1C=NC(=C2C1=NC=N2)N
SMILES (Isomeric) CN1C=NC(=C2C1=NC=N2)N
InChI InChI=1S/C6H7N5/c1-11-3-10-5(7)4-6(11)9-2-8-4/h2-3H,7H2,1H3
InChI Key FSASIHFSFGAIJM-UHFFFAOYSA-N
Popularity 13 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H7N5
Molecular Weight 149.15 g/mol
Exact Mass 149.07014524 g/mol
Topological Polar Surface Area (TPSA) 69.60 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.10
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-methylpurin-6-amine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.5614 56.14%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Nucleus 0.5246 52.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9721 97.21%
OATP1B3 inhibitior + 0.9522 95.22%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6569 65.69%
BSEP inhibitior - 0.8901 89.01%
P-glycoprotein inhibitior - 0.9823 98.23%
P-glycoprotein substrate - 0.9155 91.55%
CYP3A4 substrate - 0.7151 71.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8893 88.93%
CYP3A4 inhibition - 0.7759 77.59%
CYP2C9 inhibition - 0.9766 97.66%
CYP2C19 inhibition - 0.7399 73.99%
CYP2D6 inhibition - 0.6641 66.41%
CYP1A2 inhibition + 0.7885 78.85%
CYP2C8 inhibition - 0.9650 96.50%
CYP inhibitory promiscuity - 0.7544 75.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Danger 0.4907 49.07%
Eye corrosion - 0.9722 97.22%
Eye irritation + 0.8338 83.38%
Skin irritation + 0.6068 60.68%
Skin corrosion - 0.8288 82.88%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6814 68.14%
Micronuclear + 0.9700 97.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation - 0.9097 90.97%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7233 72.33%
Acute Oral Toxicity (c) II 0.4823 48.23%
Estrogen receptor binding - 0.9350 93.50%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.7489 74.89%
Glucocorticoid receptor binding - 0.7920 79.20%
Aromatase binding - 0.6608 66.08%
PPAR gamma - 0.8902 89.02%
Honey bee toxicity - 0.9810 98.10%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.8801 88.01%

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 94.79% 96.09%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 91.26% 93.65%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.49% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.98% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.67% 95.56%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 83.14% 93.10%
CHEMBL3401 O75469 Pregnane X receptor 81.42% 94.73%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.18% 100.00%

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.
Momordica charantia

Cross-Links

Top
PubChem 1673
LOTUS LTS0031313
wikiData Q105162255