(2R,3S,4R,5R)-2-(hydroxymethyl)-5-[6-[[(3S)-4-hydroxy-3-methylbutyl]amino]purin-9-yl]oxolane-3,4-diol

Details

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Internal ID 64045629-6005-4995-8ace-d8f919c6db80
Taxonomy Nucleosides, nucleotides, and analogues > Purine nucleosides
IUPAC Name (2R,3S,4R,5R)-2-(hydroxymethyl)-5-[6-[[(3S)-4-hydroxy-3-methylbutyl]amino]purin-9-yl]oxolane-3,4-diol
SMILES (Canonical) CC(CCNC1=C2C(=NC=N1)N(C=N2)C3C(C(C(O3)CO)O)O)CO
SMILES (Isomeric) C[C@@H](CCNC1=C2C(=NC=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O)CO
InChI InChI=1S/C15H23N5O5/c1-8(4-21)2-3-16-13-10-14(18-6-17-13)20(7-19-10)15-12(24)11(23)9(5-22)25-15/h6-9,11-12,15,21-24H,2-5H2,1H3,(H,16,17,18)/t8-,9+,11+,12+,15+/m0/s1
InChI Key DBVVQDGIJAUEAZ-OPYVMVOTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H23N5O5
Molecular Weight 353.37 g/mol
Exact Mass 353.16991885 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP 0.10
Atomic LogP (AlogP) -1.13
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3S,4R,5R)-2-(hydroxymethyl)-5-[6-[[(3S)-4-hydroxy-3-methylbutyl]amino]purin-9-yl]oxolane-3,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9093 90.93%
Caco-2 - 0.8864 88.64%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.8857 88.57%
Subcellular localzation Nucleus 0.3649 36.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9314 93.14%
OATP1B3 inhibitior + 0.9439 94.39%
MATE1 inhibitior - 0.9212 92.12%
OCT2 inhibitior - 0.8423 84.23%
BSEP inhibitior - 0.9673 96.73%
P-glycoprotein inhibitior - 0.8705 87.05%
P-glycoprotein substrate - 0.6214 62.14%
CYP3A4 substrate + 0.5119 51.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8422 84.22%
CYP3A4 inhibition - 0.9758 97.58%
CYP2C9 inhibition - 0.8927 89.27%
CYP2C19 inhibition - 0.8922 89.22%
CYP2D6 inhibition - 0.9372 93.72%
CYP1A2 inhibition - 0.9201 92.01%
CYP2C8 inhibition - 0.8944 89.44%
CYP inhibitory promiscuity - 0.9307 93.07%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6607 66.07%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9722 97.22%
Skin irritation - 0.7606 76.06%
Skin corrosion - 0.9300 93.00%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5071 50.71%
Micronuclear + 0.9600 96.00%
Hepatotoxicity - 0.6482 64.82%
skin sensitisation - 0.8764 87.64%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.8777 87.77%
Acute Oral Toxicity (c) III 0.6167 61.67%
Estrogen receptor binding + 0.6825 68.25%
Androgen receptor binding + 0.6243 62.43%
Thyroid receptor binding + 0.6473 64.73%
Glucocorticoid receptor binding - 0.5118 51.18%
Aromatase binding + 0.7887 78.87%
PPAR gamma + 0.5841 58.41%
Honey bee toxicity - 0.9228 92.28%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.6843 68.43%

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 98.46% 96.09%
CHEMBL3589 P55263 Adenosine kinase 97.83% 98.05%
CHEMBL226 P30542 Adenosine A1 receptor 94.39% 95.93%
CHEMBL3401 O75469 Pregnane X receptor 91.10% 94.73%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 90.77% 93.10%
CHEMBL2581 P07339 Cathepsin D 90.77% 98.95%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 89.82% 95.83%
CHEMBL3038469 P24941 CDK2/Cyclin A 88.80% 91.38%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 88.71% 80.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.83% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.43% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.37% 94.00%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 85.16% 96.90%
CHEMBL3979 Q03181 Peroxisome proliferator-activated receptor delta 84.58% 93.95%
CHEMBL5524 Q99873 Protein-arginine N-methyltransferase 1 83.55% 96.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.31% 91.11%
CHEMBL3137261 O14744 PRMT5/MEP50 complex 82.88% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.84% 95.89%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 82.34% 98.46%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.71% 99.23%
CHEMBL2094135 Q96BI3 Gamma-secretase 80.51% 98.05%
CHEMBL237 P41145 Kappa opioid receptor 80.36% 98.10%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 80.20% 89.67%

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.
Medicago sativa

Cross-Links

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PubChem 92143404
LOTUS LTS0137183
wikiData Q104974889