3'-Fluoro-3'-deoxythymidine 5'-monophosphate

Details

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Internal ID 3b852b5c-95ef-4eb6-91ae-66cba2633989
Taxonomy Organoheterocyclic compounds > Diazines > Pyrimidines and pyrimidine derivatives > Pyrimidones
IUPAC Name [(2R,3S,5R)-3-fluoro-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl dihydrogen phosphate
SMILES (Canonical) CC1=CN(C(=O)NC1=O)C2CC(C(O2)COP(=O)(O)O)F
SMILES (Isomeric) CC1=CN(C(=O)NC1=O)[C@H]2C[C@@H]([C@H](O2)COP(=O)(O)O)F
InChI InChI=1S/C10H14FN2O7P/c1-5-3-13(10(15)12-9(5)14)8-2-6(11)7(20-8)4-19-21(16,17)18/h3,6-8H,2,4H2,1H3,(H,12,14,15)(H2,16,17,18)/t6-,7+,8+/m0/s1
InChI Key GGCAVPJXJISBOA-XLPZGREQSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14FN2O7P
Molecular Weight 324.20 g/mol
Exact Mass 324.05226595 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP -1.40
Atomic LogP (AlogP) -0.42
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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3'-Fluoro-3'-deoxythymidine 5'-monophosphate
3'-Deoxy-3'-fluorothymidine monophosphate
UNII-K6W0IAP44B
K6W0IAP44B
3'-Fluoro-3'-deoxythymidine 5'-phosphate
5'-Thymidylic acid, 3'-deoxy-3'-fluoro-
Uridine, 2',3'-dideoxy-3'-fluoro-5-methyl-, 5'-(dihydrogen phosphate)
[(2R,3S,5R)-3-fluoro-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl dihydrogen phosphate
{[(2R,3S,5R)-3-fluoro-5-(5-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methoxy}phosphonic acid
(((2R,3S,5R)-3-fluoro-5-(5-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl)methoxy)phosphonic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3'-Fluoro-3'-deoxythymidine 5'-monophosphate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8072 80.72%
Caco-2 - 0.7926 79.26%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5920 59.20%
OATP2B1 inhibitior - 0.8635 86.35%
OATP1B1 inhibitior + 0.9532 95.32%
OATP1B3 inhibitior + 0.9399 93.99%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9424 94.24%
P-glycoprotein inhibitior - 0.8796 87.96%
P-glycoprotein substrate - 0.8668 86.68%
CYP3A4 substrate + 0.5454 54.54%
CYP2C9 substrate - 0.7741 77.41%
CYP2D6 substrate - 0.8816 88.16%
CYP3A4 inhibition - 0.7537 75.37%
CYP2C9 inhibition - 0.8022 80.22%
CYP2C19 inhibition - 0.7639 76.39%
CYP2D6 inhibition - 0.8911 89.11%
CYP1A2 inhibition - 0.8160 81.60%
CYP2C8 inhibition - 0.9093 90.93%
CYP inhibitory promiscuity - 0.7579 75.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.5237 52.37%
Eye corrosion - 0.9830 98.30%
Eye irritation - 0.9804 98.04%
Skin irritation - 0.7902 79.02%
Skin corrosion - 0.9308 93.08%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4867 48.67%
Micronuclear + 0.9800 98.00%
Hepatotoxicity + 0.8350 83.50%
skin sensitisation - 0.8523 85.23%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.5173 51.73%
Acute Oral Toxicity (c) III 0.5218 52.18%
Estrogen receptor binding - 0.6082 60.82%
Androgen receptor binding + 0.6622 66.22%
Thyroid receptor binding + 0.5646 56.46%
Glucocorticoid receptor binding - 0.4932 49.32%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.5537 55.37%
Honey bee toxicity - 0.7914 79.14%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9082 90.82%

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 96.17% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 93.90% 94.73%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 93.19% 94.01%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.73% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.19% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.69% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.04% 97.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.04% 86.92%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 88.11% 80.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.37% 99.23%
CHEMBL255 P29275 Adenosine A2b receptor 85.23% 98.59%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.12% 93.04%
CHEMBL5957 P21589 5'-nucleotidase 83.46% 97.78%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.77% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.99% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.36% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.10% 94.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.91% 94.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.75% 89.00%

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.
There are no matching plants.

Cross-Links

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PubChem 447405
LOTUS LTS0013329
wikiData Q27094127