Methylpyrrolidone

Methylpyrrolidone

SCHEMBL1996316

CC#N.CN1CCCC1=O

nearest known ligand 0.77

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ BRD4 O60885 1/20 0.77
▸ BRD2 P25440 1/20 0.77
▸ ALDH1A1 P00352 5/20 0.40
▸ GAA P10253 4/20 0.40
▸ HPGD P15428 2/20 0.40
▸ KDM4E B2RXH2 1/20 0.40
▸ GLA P06280 1/20 0.40
▸ CASP1 P29466 1/20 0.40
▸ HSD17B10 Q99714 1/20 0.40
▸ INMT O95050 2/20 0.39
▸ PIK3CD O00329 1/20 0.36
▸ MEN1 O00255 3/20 0.35
▸ MAPT P10636 3/20 0.35
▸ KMT2A Q03164 3/20 0.35
▸ PSMD14 O00487 2/20 0.35
▸ RAB9A P51151 1/20 0.35
▸ SMN1; SMN2 Q16637 1/20 0.35
▸ LMNA P02545 3/20 0.34
▸ CHRM2 P08172 3/20 0.34
▸ CHRM5 P08912 3/20 0.34

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
Methylpyrrolidone SCHEMBL27685521 0.92 BRD4 (0.65) BRD4BRD2ALDH1A1GAAHPGD
Methylpyrrolidone SCHEMBL27147112 0.92 BRD4 (0.65) BRD4BRD2ALDH1A1GAAHPGD
Methylpyrrolidone SCHEMBL8511272 0.92 BRD4 (0.65) BRD4BRD2ALDH1A1GAAHPGD
Methylpyrrolidone SCHEMBL392259 0.91 — —
Methylpyrrolidone SCHEMBL165029 0.91 BRD4 (0.94) BRD4BRD2ALDH1A1GAAHPGD
Methylpyrrolidone SCHEMBL29239623 0.88 — —
Methylpyrrolidone SCHEMBL28300602 0.88 — —
Methylpyrrolidone SCHEMBL10656247 0.88 BRD4 (0.90) BRD4BRD2ALDH1A1GAAHPGD
Methylpyrrolidone SCHEMBL28609570 0.88 — —
Methylpyrrolidone SCHEMBL1255511 0.88 BRD4 (1.00) BRD4BRD2ALDH1A1GAAINMT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115581074-A Preparation method of flexible radio frequency device based on dry transfer carbon nanotube array 中国电子科技集团公司第五十五研究所 2023-01-06 — — CN claimed
US-20180261404-A1 Printable Composition for an Ionic Gel Separation Layer For Energy Storage Devices NTHDEGREE TECHNOLOGIES WORLDWIDE INC 2018-09-13 — — US claimed
CN-115581074-A Preparation method of flexible radio frequency device based on dry transfer carbon nanotube array 中国电子科技集团公司第五十五研究所 2023-01-06 — — CN disclosed
CN-108289931-B 4' -substituted nucleoside reverse transcriptase inhibitors and preparation thereof 默沙东公司 2022-10-11 — — CN disclosed
US-20220220104-A1 PYRAZOLOPYRIDINE COMPOUND AS RET INHIBITOR AND APPLICATION THEREOF GUANGZHOU BAIYUNSHAN PHARMACEUTICAL HOLDINGS CO., LTD. BAIYUNSHAN PHARMACEUTICAL GENERAL FACTORY (CN) 2022-07-14 — — US disclosed
EP-3950685-A1 PYRAZOLOPYRIDINE COMPOUND AS RET INHIBITOR AND APPLICATION THEREOF Guangzhou Baiyunshan Pharmaceutical Holdings Co., Ltd. Baiyunshan Pharmaceutical General Factory (CN) 2022-02-09 — — EP disclosed
US-20210154221-A1 4'-SUBSTITUTED NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS AND PREPARATIONS THEREOF MERCK SHARP & DOHME CORP. (US) 2021-05-27 — — US disclosed
US-10953029-B2 4′-Substituted nucleoside reverse transcriptase inhibitors and preparations thereof MERCK SHARP & DOHME CORP. (US) 2021-03-23 — — US disclosed
EP-3352781-B1 4'-SUBSTITUTED NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS AND PREPARATIONS THEREOF MERCK SHARP & DOHME (US) 2020-12-16 — — EP disclosed
WO-2020059634-A1 INTERMEDIATE PRODUCTION METHOD 日本ゼオン株式会社 2020-03-26 — — WO disclosed
US-20190022115-A1 4'-SUBSTITUTED NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS AND PREPARATIONS THEREOF MERCK SHARP & DOHME CORP. (US) 2019-01-24 — — US disclosed
WO-2005030757-A1 QUINAZOLINE DERIVATIVES ASTRAZENECA AB (SE) 2005-04-07 — — WO disclosed
WO-2005028470-A1 QUINAZOLINE DERIVATIVES ASTRAZENECA AB (SE) 2005-03-31 — — WO disclosed
WO-2005028469-A1 QUINAZOLINE DERIVATIVES ASTRAZENECA AB (SE) 2005-03-31 — — WO disclosed
EP-1487806-A1 4-ANILINO QUINAZOLINE DERIVATIVES AS ANTIPROLIFERATIVE AGENTS Astrazeneca AB (SE) 2004-12-22 — — EP disclosed
WO-2003082831-A1 4-ANILINO QUINAZOLINE DERIVATIVES AS ANTIPROLIFERATIVE AGENTS ASTRAZENECA AB (SE) 2003-10-09 — — WO disclosed
US-5419966-A Solid support for synthesis of 3'-tailed oligonucleotides MICROPROBE CORPORATION (US) 1995-05-30 — — US disclosed
EP-0547142-A4 — MICROPROBE CORP (US) 1995-01-18 — — EP disclosed
EP-0547142-A1 SOLID SUPPORT SYNTHESIS OF 3'-TAILED OLIGONUCLEOTIDES VIA A LINKING MOLECULE EPOCH PHARMACEUTICALS, INC. (US) 1993-06-23 — — EP disclosed
WO-1992003464-A1 SOLID SUPPORT SYNTHESIS OF 3'-TAILED OLIGONUCLEOTIDES VIA A LINKING MOLECULE MICROPROBE CORPORATION (US) 1992-03-05 — — 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 (4 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-20210154221-A1 4'-SUBSTITUTED NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS AND PREPARATIONS THEREOF HPRT1, SAMHD1, DUT BRD4 1857/4885BRD2 3920/4885ALDH1A1 433/4885
US-20220220104-A1 PYRAZOLOPYRIDINE COMPOUND AS RET INHIBITOR AND APPLICATION THEREOF RET, BRAF, RAF1 BRD4 1488/4885BRD2 902/4885ALDH1A1 1309/4885
US-20190022115-A1 4'-SUBSTITUTED NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS AND PREPARATIONS THEREOF HPRT1, DUT, SAMHD1 BRD4 1971/4885BRD2 3991/4885ALDH1A1 386/4885
US-10953029-B2 4′-Substituted nucleoside reverse transcriptase inhibitors and preparations thereof DUT, HPRT1, SAMHD1 BRD4 2042/4885BRD2 4008/4885ALDH1A1 391/4885

“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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