2-Amino-4H-purin-6-ol

Details

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Internal ID c8a813b4-9df7-41b1-8f0b-fe5f4d244a39
Taxonomy Organoheterocyclic compounds > Imidazopyrimidines > Purines and purine derivatives > Purinones
IUPAC Name 2-amino-1,4-dihydropurin-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H5N5O/c6-5-9-3-2(4(11)10-5)7-1-8-3/h1,3H,(H3,6,9,10,11)
InChI Key DVSXEQQNZWZVJD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C5H5N5O
Molecular Weight 151.13 g/mol
Exact Mass 151.04940980 g/mol
Topological Polar Surface Area (TPSA) 92.20 Ų
XlogP -1.60
Atomic LogP (AlogP) -1.76
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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914452-02-1
BDBM626104

2D Structure

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2D Structure of 2-Amino-4H-purin-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 - 0.8318 83.18%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.4054 40.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9655 96.55%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9310 93.10%
P-glycoprotein inhibitior - 0.9840 98.40%
P-glycoprotein substrate - 0.9494 94.94%
CYP3A4 substrate - 0.6307 63.07%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8379 83.79%
CYP3A4 inhibition - 0.9844 98.44%
CYP2C9 inhibition - 0.9588 95.88%
CYP2C19 inhibition - 0.9154 91.54%
CYP2D6 inhibition - 0.9366 93.66%
CYP1A2 inhibition - 0.6535 65.35%
CYP2C8 inhibition - 0.9567 95.67%
CYP inhibitory promiscuity - 0.9946 99.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6938 69.38%
Eye corrosion - 0.9821 98.21%
Eye irritation - 0.7924 79.24%
Skin irritation - 0.7126 71.26%
Skin corrosion - 0.9395 93.95%
Ames mutagenesis + 0.6230 62.30%
Human Ether-a-go-go-Related Gene inhibition - 0.6656 66.56%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8873 88.73%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5689 56.89%
Acute Oral Toxicity (c) III 0.6089 60.89%
Estrogen receptor binding - 0.9118 91.18%
Androgen receptor binding - 0.7034 70.34%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.8511 85.11%
Aromatase binding - 0.6407 64.07%
PPAR gamma - 0.8172 81.72%
Honey bee toxicity - 0.7890 78.90%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity - 0.9764 97.64%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.68% 94.45%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.20% 85.30%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.14% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.25% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.97% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 83.21% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.18% 96.09%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.93% 92.88%
CHEMBL221 P23219 Cyclooxygenase-1 80.92% 90.17%

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.
Aesculus chinensis
Leonurus japonicus

Cross-Links

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PubChem 23644321
NPASS NPC287928