SCHEMBL381848

SCHEMBL381848

CC(=O)O[C@]1(C(C)=O)[C@H](O)[C@@H](CO)O[C@@]1(C(C)=O)n1ccc(N)nc1=O

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE3A Q14432 3/20 0.41
PDE4D Q08499 1/20 0.41
SLC29A1 Q99808 1/20 0.41
LMNA P02545 4/20 0.41
THRB P10828 1/20 0.41
MTOR P42345 1/20 0.41
MDM2 Q00987 1/20 0.41
NCOA1 Q15788 1/20 0.41
NCOA3 Q9Y6Q9 1/20 0.41
POLA1 P09884 1/20 0.35
CACNA1F O60840 2/20 0.33
ALB P02768 2/20 0.33
MAPT P10636 2/20 0.33
CACNA1D Q01668 2/20 0.33
CACNA1S Q13698 2/20 0.33
CACNA1C Q13936 2/20 0.33
SMN1; SMN2 Q16637 2/20 0.32
POLB P06746 1/20 0.32
ALDH1A1 P00352 1/20 0.32
L3MBTL1 Q9Y468 1/20 0.30

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
SCHEMBL8712262 0.90 POLA1 (0.38) PDE3APDE4DSLC29A1LMNATHRB
SCHEMBL12813023 0.86 DNMT1 (0.41) LMNAMTORALDH1A1
SCHEMBL6534202 0.84 PDE3A (0.45) PDE3APDE4DSLC29A1LMNATHRB
SCHEMBL27321202 0.83 PDE3A (0.44) PDE3APDE4DSLC29A1LMNATHRB
SCHEMBL29414447 0.82 PDE3A (0.42) PDE3APDE4DSLC29A1LMNATHRB
SCHEMBL31189348 0.82 PDE3A (0.48) PDE3APDE4DSLC29A1LMNATHRB
SCHEMBL60518 0.79 SLC28A1 (0.39) SLC29A1LMNAALDH1A1
SCHEMBL11664470 0.78 LMNA (0.46) PDE3APDE4DSLC29A1LMNATHRB
SCHEMBL6060293 0.77 PDE3A (0.35) PDE3APDE4DSLC29A1LMNATHRB
SCHEMBL10615248 0.77 PDE3A (0.44) PDE3APDE4DSLC29A1LMNATHRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240327447-A1 CHEMICAL SYNTHESIS OF CYTIDINE-5'-MONOPHOSPHO-N-GLYCYL-SIALIC ACID 89BIO, INC. (US) 2024-10-03 US claimed
CN-118414344-A Chemical synthesis of cytidine-5' -monophosphate-N-glycyl-sialic acid 89生物公司 2024-07-30 CN claimed
EP-4225766-A1 CHEMICAL SYNTHESIS OF CYTIDINE-5'-MONOPHOSPHO-N-GLYCYL-SIALIC ACID 89Bio, Inc. (US) 2023-08-16 EP claimed
WO-2023122616-A1 CHEMICAL SYNTHESIS OF CYTIDINE-5'-MONOPHOSPHO-N-GLYCYL-SIALIC ACID 89BIO, INC. (US) 2023-06-29 WO claimed
CN-112301118-B Method and kit for simultaneously obtaining RNA abundance and active RNA polymerase sites in full transcriptome range 浙江大学 2022-05-13 CN claimed
US-7776838-B1 Treatment of chemotherapeutic agent and antiviral agent toxicity with acylated pyrimidine nucleosides WELLSTAT THERAPEUTICS CORPORATION (US) 2010-08-17 US claimed
EP-1491201-B1 Methods of reducing toxicity of 5-fluorouracil with acylated pyrimidine nucleosides WELLSTAT THERAPEUTICS CORP (US) 2006-03-22 EP claimed
US-20040220134-A1 Pyrimidine nucleotide precursors for treatment of systemic inflammation and inflammatory hepatitis PRO-NEURON, INC. (US) 2004-11-04 US claimed
EP-0831849-A4 METHODS OF REDUCING TOXICITY OF CHEMOTHERAPEUTIC AND ANTIVIRAL AGENTS WITH ACYLATED PYRIMIDINE NUCLEOSIDES WELLSTAT THERAPEUTICS CORP (US) 2003-03-26 EP claimed
US-6344447-B2 ADMINISTERING MIXTURE OF NUCLEOSIDES; ANTICANCER AGENT PRO-NEURON, INC. 2002-02-05 US claimed
EP-0594667-B1 TREATMENT OF CHEMOTHERAPEUTIC AGENT AND ANTIVIRAL AGENT TOXICITY WITH ACYLATED PYRIMIDINE NUCLEOSIDES PRO NEURON INC (US) 2001-09-19 EP claimed
US-5968914-A Treatment of chemotherapeutic agent and antiviral agent toxicity with acylated pyrimidine nucleosides PRO-NEURON, INC. (US) 1999-10-19 US claimed
EP-0831849-A1 METHODS OF REDUCING TOXICITY OF CHEMOTHERAPEUTIC AND ANTIVIRAL AGENTS WITH ACYLATED PYRIMIDINE NUCLEOSIDES PRO-NEURON, INC. (US) 1998-04-01 EP claimed
JP-2584947-B2 1997-02-26 JP claimed
WO-1996040165-A1 METHODS OF REDUCING TOXICITY OF CHEMOTHERAPEUTIC AND ANTIVIRAL AGENTS WITH ACYLATED PYRIMIDINE NUCLEOSIDES PRO-NEURON, INC. (US) 1996-12-19 WO claimed
EP-0594667-A4 TREATMENT OF CHEMOTHERAPEUTIC AGENT AND ANTIVIRAL AGENT TOXICITY WITH ACYLATED PYRIMIDINE NUCLEOSIDES PRO NEURON INC (US) 1996-01-10 EP claimed
WO-1994026761-A1 TREATMENT OF CHEMOTHERAPEUTIC AGENT AND ANTIVIRAL AGENT TOXICITY WITH ACYLATED PYRIMIDINE NUCLEOSIDES PRO-NEURON, INC. (US) 1994-11-24 WO claimed
EP-0594667-A1 TREATMENT OF CHEMOTHERAPEUTIC AGENT AND ANTIVIRAL AGENT TOXICITY WITH ACYLATED PYRIMIDINE NUCLEOSIDES PRO-NEURON, INC. (US) 1994-05-04 EP claimed
CN-1071577-A Handle the toxicity of chemotherapy reagent and Anti-virus agent with acylated pyrimidine nucleosides PRO NEURON INC (US) 1993-05-05 CN claimed
WO-1993001202-A1 TREATMENT OF CHEMOTHERAPEUTIC AGENT AND ANTIVIRAL AGENT TOXICITY WITH ACYLATED PYRIMIDINE NUCLEOSIDES PRO-NEURON, INC. (US) 1993-01-21 WO claimed

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

For each of this compound's patents that has machine-readable text (2 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-20240327447-A1 CHEMICAL SYNTHESIS OF CYTIDINE-5'-MONOPHOSPHO-N-GLYCYL-SIALIC ACID NEU2, NEU1, FUT5 PDE3A 2399/4885PDE4D 1156/4885SLC29A1 170/4885
US-20040220134-A1 Pyrimidine nucleotide precursors for treatment of systemic inflammation and inflammatory hepatitis UMPS, PNP, TYMP PDE3A 2887/4885PDE4D 2335/4885SLC29A1 37/4885

“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.