1-(3-methylbut-2-enyl)purin-6-amine

Details

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Internal ID c7fb01a9-7c73-4d5f-8869-f72494b02ba7
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > 6-aminopurines
IUPAC Name 1-(3-methylbut-2-enyl)purin-6-amine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H13N5/c1-7(2)3-4-15-6-14-10-8(9(15)11)12-5-13-10/h3,5-6H,4,11H2,1-2H3
InChI Key IOHHJJXUINJFQB-UHFFFAOYSA-N
Popularity 0 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) 69.60 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(3-methylbut-2-enyl)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 + 0.9951 99.51%
Caco-2 + 0.6077 60.77%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4955 49.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9501 95.01%
OATP1B3 inhibitior + 0.9446 94.46%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9141 91.41%
P-glycoprotein inhibitior - 0.9589 95.89%
P-glycoprotein substrate - 0.8058 80.58%
CYP3A4 substrate - 0.6594 65.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8956 89.56%
CYP3A4 inhibition - 0.7207 72.07%
CYP2C9 inhibition - 0.6977 69.77%
CYP2C19 inhibition - 0.6408 64.08%
CYP2D6 inhibition - 0.5440 54.40%
CYP1A2 inhibition + 0.7549 75.49%
CYP2C8 inhibition - 0.8920 89.20%
CYP inhibitory promiscuity + 0.6572 65.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.4785 47.85%
Eye corrosion - 0.9811 98.11%
Eye irritation - 0.8853 88.53%
Skin irritation - 0.6606 66.06%
Skin corrosion - 0.8886 88.86%
Ames mutagenesis + 0.6046 60.46%
Human Ether-a-go-go-Related Gene inhibition - 0.4632 46.32%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.5824 58.24%
skin sensitisation - 0.8386 83.86%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.4932 49.32%
Acute Oral Toxicity (c) III 0.6154 61.54%
Estrogen receptor binding - 0.7119 71.19%
Androgen receptor binding - 0.4866 48.66%
Thyroid receptor binding - 0.5685 56.85%
Glucocorticoid receptor binding - 0.5381 53.81%
Aromatase binding + 0.7099 70.99%
PPAR gamma - 0.5742 57.42%
Honey bee toxicity - 0.9679 96.79%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8772 87.72%

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 93.15% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.19% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.81% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.40% 89.34%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.13% 93.10%

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.
Bridelia balansae

Cross-Links

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PubChem 101596827
LOTUS LTS0168902
wikiData Q105116654