SCHEMBL264019

SCHEMBL264019

C=CC(N)n1ccc(=O)[nH]c1=O

nearest known ligand 0.46

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
▸ CRBN Q96SW2 3/20 0.46
▸ DDB1 Q16531 1/20 0.38
▸ PKM P14618 1/20 0.35
▸ POLB P06746 1/20 0.33
▸ HSD17B10 Q99714 1/20 0.33
▸ DUT P33316 2/20 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
SCHEMBL2990979 0.76 CRBN (0.50) CRBNDDB1PKMPOLBHSD17B10
SCHEMBL1344880 0.76 CRBN (0.50) CRBNDDB1PKMPOLBHSD17B10
SCHEMBL669511 0.75 CRBN (0.42) CRBNDDB1PKMPOLBHSD17B10
SCHEMBL17205220 0.75 CRBN (0.38) CRBNDDB1PKMPOLBHSD17B10
SCHEMBL3993881 0.73 CRBN (0.45) CRBNDDB1POLBHSD17B10DUT
SCHEMBL27480972 0.71 CRBN (0.46) CRBNDDB1PKMPOLBHSD17B10
SCHEMBL5290093 0.71 CRBN (0.46) CRBNDDB1PKMPOLBHSD17B10
SCHEMBL2719765 0.71 CRBN (0.54) CRBNDDB1PKMPOLBHSD17B10
SCHEMBL10642564 0.71 CRBN (0.48) CRBNDDB1PKMPOLBHSD17B10
SCHEMBL669608 0.70 CYP17A1 (0.39) CRBNDDB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2294076-B1 CHEMICALLY MODIFIED NUCLEOSIDE 5'-TRIPHOSPHATES FOR THERMALLY INITIATED REPLICATION OF NUCLEIC ACID TRILINK BIOTECHNOLOGIES (US) 2017-03-08 — — EP claimed
EP-2294076-A1 CHEMICALLY MODIFIED NUCLEOSIDE 5'-TRIPHOSPHATES FOR THERMALLY INITIATED AMPLIFICATION OF NUCLEIC ACID TriLink BioTechnologies (US) 2011-03-16 — — EP claimed
US-20100003724-A1 CHEMICALLY MODIFIED NUCLEOSIDE 5'-TRIPHOSPHATES FOR THERMALLY INITIATED AMPLIFICATION OF NUCLEIC ACID TriLink Bio Technologies 2010-01-07 — — US claimed
WO-2009151921-A1 CHEMICALLY MODIFIED NUCLEOSIDE 5'-TRIPHOSPHATES FOR THERMALLY INITIATED AMPLIFICATION OF NUCLEIC ACID TRILINK BIOTECHNOLOGIES (US) 2009-12-17 — — WO claimed
US-20090011488-A1 METHODS FOR STORING COMPOSITIONS USEFUL FOR SYNTHESIZING NUCLEIC ACID MOLECULES ROSETTA INPHARMATICS, LLC (US) 2009-01-08 — — US claimed
US-20250333473-A1 CELLS LACKING B2M SURFACE EXPRESSION AND METHODS FOR ALLOGENEIC ADMINISTRATION OF SUCH CELLS HARVARD COLLEGE (US) 2025-10-30 — — US disclosed
US-12357675-B2 Efficient protein expression in vivo using modified RNA (mod-RNA) THE GENERAL HOSPITAL CORPORATION 2025-07-15 — — US disclosed
US-12180263-B2 Cells lacking B2M surface expression and methods for allogeneic administration of such cells PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2024-12-31 — — US disclosed
US-20240335551-A1 FUNCTIONAL MOIETIES AND THEIR USES AND SYNTHETIC PREPARATION OLIX US, INC. 2024-10-10 — — US disclosed
US-12054748-B2 Mammalian somatic cell with modified RNA encoding reprogramming factors CHILDREN'S MEDICAL CENTER CORPORATION (US) 2024-08-06 — — US disclosed
WO-2024151687-A1 GENETIC SWITCHES AND THEIR USE IN TREATING CANCER FLAGSHIP PIONEERING INNOVATIONS V, INC. (US) 2024-07-18 — — WO disclosed
US-20240238210-A1 POLYNUCLEOTIDES ENCODING CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR FOR THE TREATMENT OF CYSTIC FIBROSIS ARES CAPITAL CORPORATION, AS AGENT 2024-07-18 — — US disclosed
EP-1339699-A1 SUBSTITUTED AMIDOALKYL URACILS AND THE USE THEREOF Bayer Aktiengesellschaft (DE) 2003-09-03 — — EP disclosed
EP-1303497-A1 SUBSTITUTED AMIDOALKYL-URACILS AS PARP INHIBITORS Bayer Aktiengesellschaft (DE) 2003-04-23 — — EP disclosed
US-20030022905-A1 Substituted amidoalkyl-uracils and their use BAYER AKTIENGESELLSCHAFT (DE) 2003-01-30 — — US disclosed
US-20030022905-A1 Substituted amidoalkyl-uracils and their use BAYER AKTIENGESELLSCHAFT (DE) 2003-01-30 — — US disclosed
WO-2002040455-A8 SUBSTITUTED AMIDOALKYL URACILS AND THEIR USE AS INHIBITORS OF THE POLY(ADP-RIBOSE) SYNTHETASE (PARS) BAYER AG (DE) 2002-07-18 — — WO disclosed
WO-2002040455-A1 SUBSTITUTED AMIDOALKYL URACILS AND THEIR USE AS INHIBITORS OF THE POLY(ADP-RIBOSE) SYNTHETASE (PARS) BAYER AKTIENGESELLSCHAFT (DE) 2002-05-23 — — WO disclosed
WO-2002006247-A8 SUBSTITUTED AMIDOALKYL-URACILS AS PARP INHIBITORS BAYER AG (DE) 2002-02-21 — — WO disclosed
WO-2002006247-A1 SUBSTITUTED AMIDOALKYL-URACILS AS PARP INHIBITORS BAYER AKTIENGESELLSCHAFT (DE) 2002-01-24 — — WO 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-20240238210-A1 POLYNUCLEOTIDES ENCODING CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR FOR THE TREATMENT OF CYSTIC FIBROSIS CFTR, SLC47A1, TMEM205 CRBN 3966/4885DDB1 1849/4885PKM 2664/4885
US-20240335551-A1 FUNCTIONAL MOIETIES AND THEIR USES AND SYNTHETIC PREPARATION FGB, SELP, PTMS CRBN 1185/4885DDB1 3723/4885PKM 1524/4885
US-20030022905-A1 Substituted amidoalkyl-uracils and their use UNG, UMPS, TYMP CRBN 4595/4885DDB1 58/4885PKM 3951/4885

“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.

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