2-amino-4-hydroxypteridine-6-carboxylic acid

Details

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Internal ID 1dfbdb97-ed2c-4590-a974-88e0f7fe7fe4
Taxonomy Organoheterocyclic compounds > Pteridines and derivatives > Pterins and derivatives > Pterin carboxylates
IUPAC Name 2-amino-4-hydroxypteridine-6-carboxylic acid
SMILES (Canonical) C1=C(N=C2C(=N1)N=C(N=C2O)N)C(=O)O
SMILES (Isomeric) C1=C(N=C2C(=N1)N=C(N=C2O)N)C(=O)O
InChI InChI=1S/C7H5N5O3/c8-7-11-4-3(5(13)12-7)10-2(1-9-4)6(14)15/h1H,(H,14,15)(H3,8,9,11,12,13)
InChI Key QABAUCFGPWONOG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H5N5O3
Molecular Weight 207.15 g/mol
Exact Mass 207.03923904 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.59
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-amino-4-hydroxypteridine-6-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9797 97.97%
Caco-2 - 0.8944 89.44%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4578 45.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9461 94.61%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9173 91.73%
P-glycoprotein inhibitior - 0.9753 97.53%
P-glycoprotein substrate - 0.9393 93.93%
CYP3A4 substrate - 0.6672 66.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9017 90.17%
CYP3A4 inhibition - 0.8662 86.62%
CYP2C9 inhibition - 0.9450 94.50%
CYP2C19 inhibition - 0.8923 89.23%
CYP2D6 inhibition - 0.9284 92.84%
CYP1A2 inhibition - 0.7280 72.80%
CYP2C8 inhibition - 0.8736 87.36%
CYP inhibitory promiscuity - 0.9765 97.65%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8850 88.50%
Carcinogenicity (trinary) Non-required 0.6642 66.42%
Eye corrosion - 0.9934 99.34%
Eye irritation + 0.7967 79.67%
Skin irritation - 0.7817 78.17%
Skin corrosion - 0.9735 97.35%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8245 82.45%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.6729 67.29%
skin sensitisation - 0.9152 91.52%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.6141 61.41%
Acute Oral Toxicity (c) III 0.6371 63.71%
Estrogen receptor binding - 0.5647 56.47%
Androgen receptor binding - 0.7666 76.66%
Thyroid receptor binding - 0.6127 61.27%
Glucocorticoid receptor binding - 0.5113 51.13%
Aromatase binding + 0.5916 59.16%
PPAR gamma - 0.4858 48.58%
Honey bee toxicity - 0.9362 93.62%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.7229 72.29%

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
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 94.26% 83.57%
CHEMBL221 P23219 Cyclooxygenase-1 90.00% 90.17%
CHEMBL1811 P34995 Prostanoid EP1 receptor 89.75% 95.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.39% 99.23%
CHEMBL1881 P43116 Prostanoid EP2 receptor 89.02% 93.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.89% 96.09%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.67% 94.42%
CHEMBL1929 P47989 Xanthine dehydrogenase 86.90% 96.12%
CHEMBL4040 P28482 MAP kinase ERK2 86.55% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.05% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.00% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.95% 99.15%

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.
Capsicum annuum
Citrus × aurantium
Citrus deliciosa
Elettaria cardamomum

Cross-Links

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PubChem 5320887
NPASS NPC144223