SCHEMBL2169035

SCHEMBL2169035

Nc1cccc2c1CN(C(CCC(=O)O)C(=O)O)C2=O

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 4/20 0.52
ALDH1A1 P00352 2/20 0.52
HPGD P15428 2/20 0.52
MAPK1 P28482 2/20 0.52
HSD17B10 Q99714 2/20 0.52
TP53 P04637 1/20 0.52
GLA P06280 1/20 0.52
POLB P06746 1/20 0.52
CYP3A4 P08684 1/20 0.52
CYP2D6 P10635 1/20 0.52
ALOX12 P18054 1/20 0.52
NFKB1 P19838 1/20 0.52
APEX1 P27695 1/20 0.52
ALOX15 P16050 4/20 0.46
MAPT P10636 2/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
DHFR P00374 4/20 0.41
SLC19A1 P41440 3/20 0.41
TYMS P04818 2/20 0.41
CYP1A2 P05177 1/20 0.38

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
SCHEMBL14506392 1.00 KDM4E (0.52) KDM4EALDH1A1HPGDMAPK1HSD17B10
SCHEMBL501841 0.91 KDM4E (0.45) KDM4EALDH1A1HPGDMAPK1HSD17B10
SCHEMBL30001202 0.91 ALOX15 (0.46) KDM4EALDH1A1HPGDMAPK1HSD17B10
SCHEMBL502389 0.91 ALOX15 (0.46) KDM4EALDH1A1HPGDMAPK1HSD17B10
SCHEMBL30677181 0.91 KDM4E (0.45) KDM4EALDH1A1HPGDMAPK1HSD17B10
SCHEMBL15247750 0.90 KDM4E (0.44) KDM4EALDH1A1HPGDMAPK1HSD17B10
SCHEMBL12862399 0.87 KDM4E (0.41) KDM4EALDH1A1HPGDMAPK1HSD17B10
SCHEMBL7677588 0.87 ALOX15 (0.46) KDM4EALDH1A1HPGDMAPK1HSD17B10
SCHEMBL21251503 0.86 ALOX15 (0.46) KDM4EALDH1A1HPGDMAPK1HSD17B10
SCHEMBL11888309 0.85 ALOX15 (0.45) KDM4EALDH1A1HPGDMAPK1HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111298127-A Composition comprising histamine release-promoting substance and inhibitory compound, and oral solid preparation containing the same 黄泳华 2020-06-19 CN claimed
JP-4728487-B2 2011-07-20 JP claimed
JP-2002539197-A 2002-11-19 JP claimed
EP-1163219-A1 SUBSTITUTED 1-OXO- AND 1,3-DIOXOISOINDOLINES AND THEIR USE IN PHARMACEUTICAL COMPOSITIONS FOR REDUCING INFLAMMATORY CYTOKINE LEVELS CELGENE CORPORATION (US) 2001-12-19 EP claimed
WO-2000055134-A1 SUBSTITUTED 1-OXO- AND 1,3-DIOXOISOINDOLINES AND THEIR USE IN PHARMACEUTICAL COMPOSITIONS FOR REDUCING INFLAMMATORY CYTOKINE LEVELS CELGENE CORPORATION (US) 2000-09-21 WO claimed
US-20230210999-A1 TARGETED PROTEASE DEGRADATION (TED) PLATFORM EUBULUS BIOTHERAPEUTICS (HONG KONG) LIMITED (HK) 2023-07-06 US disclosed
US-20230210999-A1 TARGETED PROTEASE DEGRADATION (TED) PLATFORM EUBULUS BIOTHERAPEUTICS (HONG KONG) LIMITED (HK) 2023-07-06 US disclosed
WO-2022150561-A1 STABLE SOLUTIONS OF IMMUNOMODULATORY IMIDE COMPOUNDS FOR PARENTERAL USE STARTON THERAPEUTICS, INC. (US) 2022-07-14 WO disclosed
US-20220218687-A1 Stable Solutions of Immunomodulatory Imide Compounds for Parenteral Use STARTON THERAPEUTICS, INC. 2022-07-14 US disclosed
CN-111298127-A Composition comprising histamine release-promoting substance and inhibitory compound, and oral solid preparation containing the same 黄泳华 2020-06-19 CN disclosed
US-9522899-B2 Methods for synthesizing 3-(substituted dihydroisoindolinone-2-yl)-2, 6-dioxopiperidine, and intermediates thereof NANJIAN CAVENDISH BIO-ENGINEERING TECHNOLOGY CO., LTD (CN) 2016-12-20 US disclosed
US-9522899-B2 Methods for synthesizing 3-(substituted dihydroisoindolinone-2-yl)-2, 6-dioxopiperidine, and intermediates thereof NANJIAN CAVENDISH BIO-ENGINEERING TECHNOLOGY CO., LTD (CN) 2016-12-20 US disclosed
US-20110021567-A1 PREPARATION OF LENALIDOMIDE DR. REDDY'S LABORATORIES LTD. (IN) 2011-01-27 US disclosed
WO-2010139266-A1 METHODS FOR SYNTHESIZING 3-(SUBSTITUTED DIHYDROISOINDOLINONE-2-YL)-2,6-DIOXOPIPERIDINE, AND INTERMEDIATES THEREOF Nanjing Cavendish Bio-Engineering Technology Co., Ltd. (CN) 2010-12-09 WO disclosed
WO-2010056384-A1 LENALIDOMIDE SOLVATES AND PROCESSES DR. REDDY'S LABORATORIES LTD. (IN) 2010-05-20 WO disclosed
WO-2009114601-A2 PREPARATION OF LENALIDOMIDE DR. REDDY'S LABORATORIES LTD. (IN) 2009-09-17 WO disclosed
US-20070105903-A1 Synthesis and anti-tumor activity of nitrogen substituted thalidomide analogs CELGENE CORPORATION 2007-05-10 US disclosed
US-6380239-B1 FOR THERAPY OF ARTHRITIS, RHEUMATOID ARTHRITIS, OSTEOARTHRITIS, REPERFUSION INJURY, INFLAMMATORY BOWEL DISEASE, CROHN'S DISEASE, ULCERATIVE COLITIS, SYSTEMIC LUPUS ERYTHREMATOSIS, SCLERODERMA, APHTHOUS ULCERS, ASTHMA CELGENE CORPORATION 2002-04-30 US disclosed
EP-1163219-A1 SUBSTITUTED 1-OXO- AND 1,3-DIOXOISOINDOLINES AND THEIR USE IN PHARMACEUTICAL COMPOSITIONS FOR REDUCING INFLAMMATORY CYTOKINE LEVELS CELGENE CORPORATION (US) 2001-12-19 EP disclosed
WO-2000055134-A1 SUBSTITUTED 1-OXO- AND 1,3-DIOXOISOINDOLINES AND THEIR USE IN PHARMACEUTICAL COMPOSITIONS FOR REDUCING INFLAMMATORY CYTOKINE LEVELS CELGENE CORPORATION (US) 2000-09-21 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-20230210999-A1 TARGETED PROTEASE DEGRADATION (TED) PLATFORM UCHL3, UBE2L3, ADAM33 KDM4E 2658/4885ALDH1A1 2539/4885HPGD 4691/4885
US-20220218687-A1 Stable Solutions of Immunomodulatory Imide Compounds for Parenteral Use IL2, MYD88, MALT1 KDM4E 602/4885ALDH1A1 2825/4885HPGD 513/4885
US-20110021567-A1 PREPARATION OF LENALIDOMIDE RPS27A, PDCD2L, PML KDM4E 806/4885ALDH1A1 3535/4885HPGD 2457/4885
US-20070105903-A1 Synthesis and anti-tumor activity of nitrogen substituted thalidomide analogs VEGFA, FLT4, FLT1 KDM4E 1098/4885ALDH1A1 2713/4885HPGD 371/4885

“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.