1-alpha-L-Ribofuranosyl-4-thiouracil

Details

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Internal ID d2edc994-f4f8-4c48-a521-2bfb13ca2013
Taxonomy Nucleosides, nucleotides, and analogues > Pyrimidine nucleosides
IUPAC Name 1-[(2R,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylidenepyrimidin-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12N2O5S/c12-3-4-6(13)7(14)8(16-4)11-2-1-5(17)10-9(11)15/h1-2,4,6-8,12-14H,3H2,(H,10,15,17)/t4-,6-,7-,8+/m0/s1
InChI Key ZLOIGESWDJYCTF-YDLFOAGRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12N2O5S
Molecular Weight 260.27 g/mol
Exact Mass 260.04669266 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP -1.40
Atomic LogP (AlogP) -1.48
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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ZLOIGESWDJYCTF-YDLFOAGRSA-N
1-alpha-L-Ribofuranosyl-4-thiouracil

2D Structure

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2D Structure of 1-alpha-L-Ribofuranosyl-4-thiouracil

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8522 85.22%
Caco-2 - 0.8793 87.93%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.3990 39.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9239 92.39%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9662 96.62%
P-glycoprotein inhibitior - 0.9442 94.42%
P-glycoprotein substrate - 0.9687 96.87%
CYP3A4 substrate - 0.6009 60.09%
CYP2C9 substrate + 0.6032 60.32%
CYP2D6 substrate - 0.8664 86.64%
CYP3A4 inhibition - 0.9108 91.08%
CYP2C9 inhibition - 0.8360 83.60%
CYP2C19 inhibition - 0.8315 83.15%
CYP2D6 inhibition - 0.9218 92.18%
CYP1A2 inhibition - 0.8393 83.93%
CYP2C8 inhibition - 0.9637 96.37%
CYP inhibitory promiscuity - 0.8402 84.02%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Danger 0.4618 46.18%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.9672 96.72%
Skin irritation - 0.7660 76.60%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5878 58.78%
Micronuclear + 1.0000 100.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.8461 84.61%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.7883 78.83%
Acute Oral Toxicity (c) III 0.6768 67.68%
Estrogen receptor binding - 0.5478 54.78%
Androgen receptor binding + 0.7678 76.78%
Thyroid receptor binding + 0.5318 53.18%
Glucocorticoid receptor binding + 0.7688 76.88%
Aromatase binding - 0.5778 57.78%
PPAR gamma + 0.7407 74.07%
Honey bee toxicity - 0.8823 88.23%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.6806 68.06%

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 95.40% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 93.50% 95.93%
CHEMBL2581 P07339 Cathepsin D 93.05% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.51% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.15% 91.11%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.13% 86.92%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.68% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 82.23% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.15% 95.56%
CHEMBL255 P29275 Adenosine A2b receptor 80.87% 98.59%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.49% 89.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 22865605
LOTUS LTS0102288
wikiData Q105379009