Pomalidomide

Pomalidomide

SCHEMBL369172

Nc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CRBNCUL4ADDB1RBX1

The experimentally established mechanism targets of Pomalidomide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CRBN known ✓ Q96SW2 18/20 1.00
DDB1 known ✓ Q16531 17/20 1.00
IKZF3 Q9UKT9 3/20 1.00
TNF P01375 2/20 1.00
IL1B P01584 2/20 1.00
IKZF1 Q13422 2/20 1.00
TBXA2R P21731 1/20 1.00
ALDH1A1 P00352 1/20 0.74
CHRM2 P08172 1/20 0.74
OPRM1 P35372 1/20 0.74
CYP1A2 P05177 1/20 0.74
TSHR P16473 1/20 0.74
TDP1 Q9NUW8 1/20 0.74
BRD4 O60885 1/20 0.62
HDAC1 Q13547 1/20 0.59
HDAC2 Q92769 1/20 0.59

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
Pomalidomide SCHEMBL29382107 1.00 CRBN (1.00) CRBNDDB1IKZF3TNFIL1B
Pomalidomide SCHEMBL15930059 1.00 CRBN (1.00) CRBNDDB1IKZF3TNFIL1B
Pomalidomide SCHEMBL563317 1.00 CRBN (1.00) CRBNDDB1IKZF3TNFIL1B
Pomalidomide SCHEMBL15930061 1.00 CRBN (1.00) CRBNDDB1IKZF3TNFIL1B
Pomalidomide SCHEMBL931134 1.00 CRBN (1.00) CRBNDDB1IKZF3TNFIL1B
Pomalidomide SCHEMBL15930065 1.00 CRBN (1.00) CRBNDDB1IKZF3TNFIL1B
Pomalidomide SCHEMBL19250920 1.00 CRBN (1.00) CRBNDDB1IKZF3TNFIL1B
Pomalidomide SCHEMBL20525239 0.99 CRBN (0.97) CRBNDDB1IKZF3TNFIL1B
Pomalidomide SCHEMBL20525246 0.99 CRBN (0.97) CRBNDDB1IKZF3TNFIL1B
Pomalidomide SCHEMBL20525238 0.99 CRBN (0.97) CRBNDDB1IKZF3TNFIL1B

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

Appears in 15005 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4748376-A2 METHODS OF TREATING CANCERS AND ENHANCING EFFICACY OF T CELL REDIRECTING THERAPEUTICS Janssen Biotech, Inc. (US) 2026-05-27 EP claimed
WO-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO claimed
US-20260139071-A1 Subcutaneous Formulations Of Anti-CD38 Antibodies And Their Uses JANSSEN BIOTECH INC (US) 2026-05-21 US claimed
US-20260137794-A1 LIGAND-DRUG CONJUGATE AND USE THEREOF SYSTIMMUNE INC (US) 2026-05-21 US claimed
US-20260137677-A1 PROTACS USEFUL AGAINST THE MAIN PROTEASE SARS-COV-2 TOCRIS COOKSON LTD (GB) 2026-05-21 US claimed
EP-3841097-B1 2,6-BIS(((1H-BENZO[D]IMIDAZOL-2-YL)THIO)METHYL)PYRIDINE AND N2,N6-DIBENZYLPYRIDINE-2,6-DICARBOXAMIDE DERIVATIVES AND RELATED COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE (PI3K) INHIBITORS FOR TREATING CANCER BIOMEDICAL RES FOUNDATION OF THE ACADEMY OF ATHENS BRFAA (GR) 2026-05-20 EP claimed
EP-4744680-A1 TARGETED CHEMICAL DRUG AND PREPARATION METHOD THEREFOR, PHARMACEUTICAL COMPOSITION, AND USE OF TARGETED CHEMICAL DRUG Bai Yao Zhi Da (Beijing) Nanobio Technology Co., Ltd. (CN) 2026-05-20 EP claimed
CN-122059934-A PD-L1 protein degradation targeting chimeric and preparation method and application thereof 首都医科大学 2026-05-19 CN claimed
WO-2026099594-A1 THERAPEUTIC BIFUNCTIONAL AGENTS INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL (GB) 2026-05-15 WO claimed
CN-122055366-A GCN2 and PERK kinase modulators and methods of use thereof 德西费拉制药有限责任公司 2026-05-15 CN claimed
US-20030045552-A1 Isoindole-imide compounds, compositions, and uses thereof CELGENE CORPORATION 2003-03-06 US claimed
EP-1285916-A1 Substituted 2-(2,6-dioxopiperidin-3-yl)-phthalimides and -1-oxoisoindolines and method of reducing TNF alpha levels CELGENE CORPORATION (US) 2003-02-26 EP claimed
EP-0925294-B1 SUBSTITUTED 2(2,6-DIOXOPIPERIDIN-3-YL)PHTHALIMIDES AND -1-OXOISOINDOLINES AND METHOD OF REDUCING TNF-ALPHA LEVELS CELGENE CORP (US) 2002-12-11 EP 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
EP-1242082-A1 METHODS AND COMPOSITIONS FOR THE PREVENTION AND TREATMENT OF ATHEROSCLEROSIS, RESTENOSIS AND RELATED DISORDERS CELGENE CORPORATION (US) 2002-09-25 EP claimed
WO-2002059106-A1 ISOINDOLE-IMIDE COMPOUNDS, COMPOSITIONS, AND USES THEREOF CELGENE CORPORATION (US) 2002-08-01 WO claimed
US-20020054899-A1 Methods and compositions for the prevention and treatment of atherosclerosis, restenosis and related disorders CELGENE CORP. 2002-05-09 US claimed
US-20020045643-A1 Isoindolines, method of use, and pharmaceutical compositions MULLER GEORGE W (US) 2002-04-18 US claimed
WO-2001043743-A1 METHODS AND COMPOSITIONS FOR THE PREVENTION AND TREATMENT OF ATHEROSCLEROSIS, RESTENOSIS AND RELATED DISORDERS CELGENE CORP. (US) 2001-06-21 WO claimed
US-5635517-A Method of reducing TNFα levels with amino substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxo-and 1,3-dioxoisoindolines CELGENE CORPORATION (US) 1997-06-03 US claimed