2-methoxy-3-methylpurin-6-amine

Details

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Internal ID 7878e13f-3824-4ffb-9231-6e51ee3218b7
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > 6-aminopurines
IUPAC Name 2-methoxy-3-methylpurin-6-amine
SMILES (Canonical) CN1C2=NC=NC2=C(N=C1OC)N
SMILES (Isomeric) CN1C2=NC=NC2=C(N=C1OC)N
InChI InChI=1S/C7H9N5O/c1-12-6-4(9-3-10-6)5(8)11-7(12)13-2/h3H,8H2,1-2H3
InChI Key LBEZAAAVJBINPH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9N5O
Molecular Weight 179.18 g/mol
Exact Mass 179.08070993 g/mol
Topological Polar Surface Area (TPSA) 78.80 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.09
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 - 0.7357 73.57%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Lysosomes 0.5369 53.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9660 96.60%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.8819 88.19%
BSEP inhibitior - 0.8796 87.96%
P-glycoprotein inhibitior - 0.9765 97.65%
P-glycoprotein substrate - 0.8709 87.09%
CYP3A4 substrate - 0.5641 56.41%
CYP2C9 substrate - 0.7829 78.29%
CYP2D6 substrate - 0.8660 86.60%
CYP3A4 inhibition - 0.8900 89.00%
CYP2C9 inhibition - 0.9692 96.92%
CYP2C19 inhibition - 0.9260 92.60%
CYP2D6 inhibition - 0.8602 86.02%
CYP1A2 inhibition + 0.7891 78.91%
CYP2C8 inhibition - 0.9430 94.30%
CYP inhibitory promiscuity - 0.9578 95.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4851 48.51%
Eye corrosion - 0.9843 98.43%
Eye irritation + 0.6619 66.19%
Skin irritation - 0.7550 75.50%
Skin corrosion - 0.9465 94.65%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7278 72.78%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.6846 68.46%
skin sensitisation - 0.9185 91.85%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.5573 55.73%
Acute Oral Toxicity (c) II 0.5216 52.16%
Estrogen receptor binding - 0.8972 89.72%
Androgen receptor binding - 0.5408 54.08%
Thyroid receptor binding - 0.6581 65.81%
Glucocorticoid receptor binding - 0.6774 67.74%
Aromatase binding - 0.5515 55.15%
PPAR gamma - 0.8956 89.56%
Honey bee toxicity - 0.9386 93.86%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.7358 73.58%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.08% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.89% 94.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 89.96% 93.65%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.36% 86.33%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.90% 94.42%
CHEMBL2243 O00519 Anandamide amidohydrolase 84.98% 97.53%
CHEMBL235 P37231 Peroxisome proliferator-activated receptor gamma 83.42% 95.39%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.26% 96.00%
CHEMBL4040 P28482 MAP kinase ERK2 83.23% 83.82%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.56% 96.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.63% 95.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.16% 100.00%
CHEMBL290 Q13370 Phosphodiesterase 3B 80.04% 94.00%

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.
Scleromitrion diffusum

Cross-Links

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PubChem 10442272
NPASS NPC254717
LOTUS LTS0065623
wikiData Q105149220