2-(3-methylbut-3-enyl)-7H-purin-6-amine

Details

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Internal ID 2bf76049-c8a6-401f-836a-58d2f1196f89
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > 6-aminopurines
IUPAC Name 2-(3-methylbut-3-enyl)-7H-purin-6-amine
SMILES (Canonical) CC(=C)CCC1=NC(=C2C(=N1)N=CN2)N
SMILES (Isomeric) CC(=C)CCC1=NC(=C2C(=N1)N=CN2)N
InChI InChI=1S/C10H13N5/c1-6(2)3-4-7-14-9(11)8-10(15-7)13-5-12-8/h5H,1,3-4H2,2H3,(H3,11,12,13,14,15)
InChI Key GCUVWBFOTMJVLI-UHFFFAOYSA-N
Popularity 1,581 references in papers

Physical and Chemical Properties

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Molecular Formula C10H13N5
Molecular Weight 203.24 g/mol
Exact Mass 203.11709544 g/mol
Topological Polar Surface Area (TPSA) 80.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.44
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3-methylbut-3-enyl)-7H-purin-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 + 0.9887 98.87%
Caco-2 - 0.6503 65.03%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Nucleus 0.5181 51.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9311 93.11%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.8169 81.69%
P-glycoprotein inhibitior - 0.9780 97.80%
P-glycoprotein substrate - 0.6502 65.02%
CYP3A4 substrate - 0.5658 56.58%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.8491 84.91%
CYP3A4 inhibition - 0.8556 85.56%
CYP2C9 inhibition - 0.8046 80.46%
CYP2C19 inhibition - 0.8492 84.92%
CYP2D6 inhibition - 0.9164 91.64%
CYP1A2 inhibition + 0.6264 62.64%
CYP2C8 inhibition - 0.6681 66.81%
CYP inhibitory promiscuity - 0.5980 59.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5643 56.43%
Eye corrosion - 0.9862 98.62%
Eye irritation - 0.8474 84.74%
Skin irritation - 0.7010 70.10%
Skin corrosion - 0.8998 89.98%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4582 45.82%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8292 82.92%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7983 79.83%
Acute Oral Toxicity (c) III 0.5696 56.96%
Estrogen receptor binding - 0.7598 75.98%
Androgen receptor binding - 0.5692 56.92%
Thyroid receptor binding - 0.4892 48.92%
Glucocorticoid receptor binding - 0.5795 57.95%
Aromatase binding - 0.6339 63.39%
PPAR gamma - 0.5281 52.81%
Honey bee toxicity - 0.8945 89.45%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8770 87.70%

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 96.43% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.95% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 89.66% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.27% 91.11%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.10% 90.24%
CHEMBL4208 P20618 Proteasome component C5 85.52% 90.00%
CHEMBL2581 P07339 Cathepsin D 84.91% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.51% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.51% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.25% 94.45%
CHEMBL290 Q13370 Phosphodiesterase 3B 82.72% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.93% 86.33%

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.
Arabidopsis thaliana

Cross-Links

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PubChem 10352842
LOTUS LTS0115846
wikiData Q105106319