SCHEMBL562430

SCHEMBL562430

CC1(C)O[C@@H]2[C@H](O1)[C@@H](CO)O[C@H]2n1ccc(=O)[nH]c1=O

nearest known ligand 0.62

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
SLC28A1 O00337 1/20 0.62
SLC28A2 O43868 1/20 0.62
SLC29A1 Q99808 1/20 0.62
SLC28A3 Q9HAS3 1/20 0.62
P2RY14 Q15391 4/20 0.47
ALDH1A1 P00352 1/20 0.47
LMNA P02545 1/20 0.47
TDP1 Q9NUW8 1/20 0.47
P2RY2 P41231 8/20 0.46
PI4KA P42356 1/20 0.46
PI4K2B Q8TCG2 1/20 0.46
PI4K2A Q9BTU6 1/20 0.46
PI4KB Q9UBF8 1/20 0.46
P2RY6 Q15077 4/20 0.44
P2RY4 P51582 2/20 0.43

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL13901303 1.00 SLC28A1 (0.62) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL14929176 1.00 SLC28A1 (0.62) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL30534760 1.00 SLC28A1 (0.62) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL28746706 1.00 SLC28A1 (0.62) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL4083531 1.00 SLC28A1 (0.62) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL10072865 1.00 SLC28A1 (0.62) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL24780347 1.00 SLC28A1 (0.62) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL12143854 1.00 SLC28A1 (0.62) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL22236624 1.00 SLC28A1 (0.62) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL21055679 1.00 SLC28A1 (0.62) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 112 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122011028-A Method for efficiently preparing various substituted chiral phosphoramides 上海交通大学 2026-05-12 CN claimed
US-12577270-B2 2′,3′-diacetyluridine substituted with acetoacetyl at the 5′ position PHARMA CINQ, LLC (US) 2026-03-17 US claimed
CN-119613475-A Preparation method of copper-catalyzed asymmetric synthesis nucleoside prodrug intermediate or prodrug based on P (V) precursor 上海交通大学 2025-03-14 CN claimed
US-20230357304-A1 2′,3′-Diacetyluridine Substituted With Acetoacetyl at the 5′ Position WELLSTAT THERAPEUTICS CORPORATION 2023-11-09 US claimed
EP-4210709-A1 2',3'-DIACETYLURIDINE SUBSTITUTED WITH ACETOACETYL AT THE 5' POSITION Wellstat Therapeutics Corporation (US) 2023-07-19 EP claimed
CN-116157133-A 2',3' -diacetyluridine substituted with acetoacetyl group at 5' position 维尔斯达医疗公司 2023-05-23 CN claimed
JP-60066953-A None JP disclosed
CN-122011028-A Method for efficiently preparing various substituted chiral phosphoramides 上海交通大学 2026-05-12 CN disclosed
US-12577270-B2 2′,3′-diacetyluridine substituted with acetoacetyl at the 5′ position PHARMA CINQ, LLC (US) 2026-03-17 US disclosed
US-20260055125-A1 LIGAND-ASSISTED DEOXYGENATION OF PHOSPHATES TO FORM NITROGEN-CONTAINING PHOSPHORUS(V) PRECURSORS AND THEIR SUBSEQUENT CONVERSION TO VARIOUS OXYPHOSPHORUS COMPOUNDS UNIV DRESDEN TECH (DE) 2026-02-26 US disclosed
CN-119613475-A Preparation method of copper-catalyzed asymmetric synthesis nucleoside prodrug intermediate or prodrug based on P (V) precursor 上海交通大学 2025-03-14 CN disclosed
CN-119528981-A Chiral phosphonate compound and derivative thereof, preparation method, pesticide bacteriostat and application 贵州大学 2025-02-28 CN disclosed
US-12054768-B2 Methods for detecting agglutination and compositions for use in practicing the same THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-08-06 US disclosed
EP-0111299-B1 FLUORINE-CONTAINING URIDINE DERIVATIVE AND PREPARATION AND USE THEREOF Daikin Kogyo Co., Ltd. (JP) 1986-04-02 EP disclosed
US-4542209-A Fluorine-containing uridine derivative and preparation and use thereof DAIKIN KOGYO CO., LTD. (JP) 1985-09-17 US disclosed
US-4542209-A Fluorine-containing uridine derivative and preparation and use thereof DAIKIN KOGYO CO., LTD. (JP) 1985-09-17 US disclosed
JP-S6066953-A BITTERING AGENT YAMASA SHOYU CO LTD 1985-04-17 JP disclosed
EP-0111299-A1 Fluorine-containing uridine derivative and preparation and use thereof Daikin Kogyo Co., Ltd. (JP) 1984-06-20 EP disclosed
EP-0111299-A1 Fluorine-containing uridine derivative and preparation and use thereof Daikin Kogyo Co., Ltd. (JP) 1984-06-20 EP disclosed
US-4056673-A VIRICIDE, ANTINEOPLASTIC HOFFMANN-LA ROCHE INC. (US) 1977-11-01 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20260055125-A1 LIGAND-ASSISTED DEOXYGENATION OF PHOSPHATES TO FORM NITROGEN-CONTAINING PHOSPHORUS(V) PRECURSORS AND THEIR SUBSEQUENT CONVERSION TO VARIOUS OXYPHOSPHORUS COMPOUNDS CA2, CA4, CA6 SLC28A1 462/4885SLC28A2 406/4885SLC29A1 254/4885
US-12577270-B2 2′,3′-diacetyluridine substituted with acetoacetyl at the 5′ position UQCRC2, ACAT1, ACAA2 SLC28A1 441/4885SLC28A2 268/4885SLC29A1 307/4885
US-20230357304-A1 2′,3′-Diacetyluridine Substituted With Acetoacetyl at the 5′ Position ACAT1, ACADVL, ACAA2 SLC28A1 1416/4885SLC28A2 1134/4885SLC29A1 1327/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.