SCHEMBL476905

SCHEMBL476905

CC1(N2C(=O)c3cccc(N)c3C2=O)CCC(=O)NC1=O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CRBN Q96SW2 7/20 0.74
▸ DDB1 Q16531 6/20 0.74
▸ TNF P01375 2/20 0.48
▸ IL1B P01584 2/20 0.48
▸ IKZF1 Q13422 2/20 0.48
▸ IKZF3 Q9UKT9 2/20 0.48
▸ TBXA2R P21731 1/20 0.48
▸ DPP4 P27487 1/20 0.40
▸ ADORA2A P29274 1/20 0.40
▸ HSPA1A P0DMV8 1/20 0.39
▸ PABPC1 P11940 1/20 0.39
▸ BRD4 O60885 1/20 0.38
▸ HTR2B P41595 2/20 0.37
▸ TMEM97 Q5BJF2 2/20 0.37
▸ HTR3E A5X5Y0 1/20 0.37
▸ HTR3B O95264 1/20 0.37
▸ HTR3A P46098 1/20 0.37
▸ HTR3D Q70Z44 1/20 0.37
▸ HTR3C Q8WXA8 1/20 0.37
▸ ATM Q13315 2/20 0.36

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
SCHEMBL30896328 1.00 CRBN (0.74) CRBNDDB1TNFIL1BIKZF1
SCHEMBL1962200 1.00 CRBN (0.74) CRBNDDB1TNFIL1BIKZF1
SCHEMBL4674905 1.00 CRBN (0.74) CRBNDDB1TNFIL1BIKZF1
SCHEMBL2049089 0.89 DDB1 (0.74) CRBNDDB1TNFIL1BIKZF1
SCHEMBL6179617 0.89 DDB1 (0.74) CRBNDDB1TNFIL1BIKZF1
SCHEMBL2049091 0.89 DDB1 (0.74) CRBNDDB1TNFIL1BIKZF1
SCHEMBL14533518 0.88 CRBN (0.64) CRBNDDB1TNFIL1BIKZF1
SCHEMBL8259914 0.87 CRBN (0.57) CRBNDDB1TNFIL1BIKZF1
SCHEMBL13699738 0.87 DDB1 (0.57) CRBNDDB1TNFIL1BIKZF1
SCHEMBL17169674 0.86 CRBN (0.72) CRBNDDB1IKZF3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160096818-A1 SUBSTITUTED 2-(2,6-DIOXOPIPERIDIN-3-YL)-PHTHALIMIDES AND -1-OXOISOINDOLINES AND METHOD OF REDUCING TNFALPHA LEVELS CELGENE CORPORATION 2016-04-07 — — US claimed
US-20140187584-A1 Substituted 2-(2,6-Dioxopiperidin-3-yl)-phthalimides and -1-Oxoisoindolines and Method of Reducing TNFalpha Levels CELGENE CORPORATION (US) 2014-07-03 — — US claimed
US-20130030021-A1 Substituted 2-(2,6-Dioxopiperidin-3-yl)-phthalimides and 1-Oxoisoindolines and Method of Reducing TNFalpha Levels CELGENE CORPORATION (US) 2013-01-31 — — US claimed
EP-2168958-A1 Isoindole-Imide Compounds, Compositions And Uses Thereof CELGENE CORPORATION (US) 2010-03-31 — — EP claimed
EP-2070920-A1 Substituted 2-(2,6-dioxopiperidin-3-yl)-phthalimides and 1-oxoisoindolines and method of reducing TNF alpha levels CELGENE CORPORATION (US) 2009-06-17 — — EP claimed
US-7459466-B2 Substituted 2-(2,6-dioxopiperidin-3-yl)-phthalimides and -1-oxoisoindolines and method of reducing TNFα levels CELGENE CORPORATION (US) 2008-12-02 — — US claimed
EP-1486496-B1 Substituted 2-(2,6-Dioxopiperidin-3-yl)-Phthalimides and method fo reducing TNF alpha levels CELGENE CORP (US) 2008-07-16 — — EP claimed
US-20080161360-A1 Methods of using and compositions comprising immunomodulatory compounds for the treatment and management of myelodysplastic syndromes CELGENE CORPORATION 2008-07-03 — — US claimed
EP-1848433-A2 METHODS AND COMPOSITIONS USING 4-AMINO-2-(3-METHYL-2,6-DIOXOPIPERIDIN-3-YL)-ISOINDOLE-1-3-DIONE CELGENE CORPORATION (US) 2007-10-31 — — EP claimed
US-20060205787-A1 Methods and compositions using 4-amino-2-(3-methyl-2,6-dioxopiperidin-3-yl)-isoindole-1,3-dione MULLER GEORGE W 2006-09-14 — — US claimed
WO-2006081251-A2 METHODS AND COMPOSITIONS USING 4-AMINO-2-(3-METHYL-2,6-DIOXOPIPERIDIN-3-YL)-ISOINDOLE-1-3-DIONE CELGENE CORPORATION (US) 2006-08-03 — — WO claimed
US-20050131024-A1 Substituted 2-(2,6-dioxopiperidin-3-yl)-phthalimides and -1-oxoisoindolines and method of reducing TNFalpha levels CELGENE CORPORATION 2005-06-16 — — US claimed
EP-1363900-A1 ISOINDOLE-IMIDE COMPOUNDS AS TNF-INHIBITORS CELGENE CORPORATION (US) 2003-11-26 — — EP claimed
US-20030144325-A1 Isoindolines, method of use, and pharmaceutical compositions MULLER GEORGE W (US) 2003-07-31 — — US claimed
US-20030096841-A1 Isoindole-imide compounds, compositions, and uses thereof CELGENE CORPORATION 2003-05-22 — — US claimed
US-20020183360-A1 Substituted 2-(2,6-dioxopiperidin-3-YL)-phthalimides and -1-oxoisoindolines and method of reducing TNFalpha levels MULLER GEORGE W (US) 2002-12-05 — — US claimed
WO-2002059106-A1 ISOINDOLE-IMIDE COMPOUNDS, COMPOSITIONS, AND USES THEREOF CELGENE CORPORATION (US) 2002-08-01 — — WO claimed
US-20020045643-A1 Isoindolines, method of use, and pharmaceutical compositions MULLER GEORGE W (US) 2002-04-18 — — US claimed
EP-0925294-A1 SUBSTITUTED 2(2,6-DIOXOPIPERIDIN-3-YL)PHTHALIMIDES AND -1-OXOISOINDOLINES AND METHOD OF REDUCING TNF-ALPHA LEVELS CELGENE CORPORATION (US) 1999-06-30 — — EP claimed
WO-1998003502-A1 SUBSTITUTED 2(2,6-DIOXOPIPERIDIN-3-YL)PHTHALIMIDES AND -1-OXOISOINDOLINES AND METHOD OF REDUCING TNF-ALPHA LEVELS CELGENE CORPORATION (US) 1998-01-29 — — 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 (10 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-20160096818-A1 SUBSTITUTED 2-(2,6-DIOXOPIPERIDIN-3-YL)-PHTHALIMIDES AND -1-OXOISOINDOLINES AND METHOD OF REDUCING TNFALPHA LEVELS TNF, NFKBIA, TRAF2 CRBN 3501/4885DDB1 447/4885TNF 1/4885
US-20030144325-A1 Isoindolines, method of use, and pharmaceutical compositions TNF, INA, VIP CRBN 4462/4885DDB1 3090/4885TNF 1/4885
US-20140187584-A1 Substituted 2-(2,6-Dioxopiperidin-3-yl)-phthalimides and -1-Oxoisoindolines and Method of Reducing TNFalpha Levels TNF, NFKBIA, TRAF2 CRBN 3501/4885DDB1 447/4885TNF 1/4885
US-20030096841-A1 Isoindole-imide compounds, compositions, and uses thereof TNF, IKZF3, IKZF1 CRBN 1511/4885DDB1 3650/4885TNF 1/4885
US-20080161360-A1 Methods of using and compositions comprising immunomodulatory compounds for the treatment and management of myelodysplastic syndromes IL2, MCL1, MYD88 CRBN 1257/4885DDB1 1332/4885TNF 466/4885
US-20060205787-A1 Methods and compositions using 4-amino-2-(3-methyl-2,6-dioxopiperidin-3-yl)-isoindole-1,3-dione HTR5A, IDO1, HTR3C CRBN 1786/4885DDB1 2398/4885TNF 3851/4885
US-20020183360-A1 Substituted 2-(2,6-dioxopiperidin-3-YL)-phthalimides and -1-oxoisoindolines and method of reducing TNFalpha levels TNF, TNFRSF1A, TRAF2 CRBN 3437/4885DDB1 1125/4885TNF 1/4885
US-20020045643-A1 Isoindolines, method of use, and pharmaceutical compositions TNF, OPRK1, OPRD1 CRBN 4469/4885DDB1 3697/4885TNF 1/4885
US-20130030021-A1 Substituted 2-(2,6-Dioxopiperidin-3-yl)-phthalimides and 1-Oxoisoindolines and Method of Reducing TNFalpha Levels TNF, NFKBIA, TRAF2 CRBN 3601/4885DDB1 396/4885TNF 1/4885
US-20050131024-A1 Substituted 2-(2,6-dioxopiperidin-3-yl)-phthalimides and -1-oxoisoindolines and method of reducing TNFalpha levels TNF, TNFRSF1A, IL1A CRBN 3510/4885DDB1 1386/4885TNF 1/4885

“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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