SCHEMBL19973047

SCHEMBL19973047

O=C1CCC(N2Cc3c(I)cccc3C2=O)C(=O)N1

nearest known ligand 0.77

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CRBN Q96SW2 14/20 0.77
IKZF3 Q9UKT9 5/20 0.75
TNF P01375 4/20 0.75
IKZF1 Q13422 3/20 0.75
DDB1 Q16531 3/20 0.75
IL1B P01584 3/20 0.75
BRD4 O60885 1/20 0.75
CSNK1A1 P48729 1/20 0.56
ALDH1A1 P00352 1/20 0.56
CHRM2 P08172 1/20 0.56
OPRM1 P35372 1/20 0.56
CYP1A2 P05177 1/20 0.56
TSHR P16473 1/20 0.56
TDP1 Q9NUW8 1/20 0.56
MAP1LC3B Q9GZQ8 1/20 0.54
IKZF2 Q9UKS7 2/20 0.53

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
SCHEMBL25031818 1.00 CRBN (0.77) CRBNIKZF3TNFIKZF1DDB1
SCHEMBL23565076 0.91 CRBN (0.72) CRBNIKZF3TNFIKZF1DDB1
SCHEMBL29767481 0.89 CRBN (0.61) CRBNIKZF3TNFIKZF1DDB1
SCHEMBL31727916 0.87 CRBN (1.00) CRBNIKZF3TNFIKZF1DDB1
SCHEMBL29453150 0.87 CRBN (1.00) CRBNIKZF3TNFIKZF1DDB1
SCHEMBL1097880 0.87 CRBN (1.00) CRBNIKZF3TNFIKZF1DDB1
SCHEMBL20442491 0.87 CRBN (1.00) CRBNIKZF3TNFIKZF1DDB1
SCHEMBL868592 0.86 CRBN (0.75) CRBNIKZF3TNFIKZF1DDB1
SCHEMBL21462288 0.86 CRBN (0.75) CRBNIKZF3TNFIKZF1DDB1
SCHEMBL21602701 0.86 CRBN (0.75) CRBNIKZF3TNFIKZF1DDB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12569564-B2 Spirocyclic MDM2 modulator and uses thereof NEWAVE PHARMACEUTICAL INC. (US) 2026-03-10 US disclosed
EP-4676929-A1 PROTAC DEGRADERS OF MLLT1 AND/OR MLLT3 Dark Blue Therapeutics Ltd (GB) 2026-01-14 EP disclosed
WO-2025262297-A1 PROTAC DEGRADERS OF MLLT1 AND/OR MLLT3 DARK BLUE THERAPEUTICS LTD (GB) 2025-12-26 WO disclosed
WO-2025262295-A1 PROTAC DEGRADERS OF MLLT1 AND/OR MLLT3 DARK BLUE THERAPEUTICS LTD (GB) 2025-12-26 WO disclosed
EP-4667467-A1 PROTAC DEGRADERS OF MLLT1 AND/OR MLLT3 Dark Blue Therapeutics Ltd (GB) 2025-12-24 EP disclosed
EP-4667466-A1 PROTAC DEGRADERS OF MLLT1 AND/OR MLLT3 Dark Blue Therapeutics Ltd (GB) 2025-12-24 EP disclosed
US-20250154157-A1 HETEROCYCLIC COMPOUNDS USEFUL FOR TREATING A ERK5-MEDIATED DISEASE CANCER RESEARCH TECH LTD (GB) 2025-05-15 US disclosed
US-20250073340-A1 SPIROCYCLIC MDM2 MODULATOR AND USES THEREOF NEWAVE PHARMACEUTICAL INC. 2025-03-06 US disclosed
EP-4479400-A1 HETEROCYCLIC COMPOUNDS USEFUL FOR TREATING A ERK5-MEDIATED DISEASE Cancer Research Technology Limited (GB) 2024-12-25 EP disclosed
CN-119053604-A Heterocyclic compounds for the treatment of ERK5 mediated diseases 癌症研究技术有限公司 2024-11-29 CN disclosed
WO-2020239103-A1 BTK INHIBITOR RING DERIVATIVE, PREPARATION METHOD THEREFOR AND PHARMACEUTICAL APPLICATION THEREOF 四川海思科制药有限公司 2020-12-03 WO disclosed
US-20200277305-A1 BET Bromodomain Protein Degraders with Cleavable Linkers NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2020-09-03 US disclosed
WO-2020142227-A1 ESTROGEN RECEPTOR PROTEIN DEGRADERS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2020-07-09 WO disclosed
WO-2020038415-A1 TROPOMYOSIN RECEPTOR KINASE (TRK) DEGRADATION COMPOUNDS AND METHODS OF USE CULLGEN (SHANGHAI), INC. (CN) 2020-02-27 WO disclosed
US-20190263827-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS UNIV MICHIGAN REGENTS (US) 2019-08-29 US disclosed
US-20190263827-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS UNIV MICHIGAN REGENTS (US) 2019-08-29 US disclosed
EP-3512853-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS The Regents of The University of Michigan (US) 2019-07-24 EP disclosed
WO-2019055444-A1 BET BROMODOMAIN PROTEIN DEGRADERS WITH CLEAVABLE LINKERS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2019-03-21 WO disclosed
WO-2018052949-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2018-03-22 WO disclosed
WO-2018052949-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2018-03-22 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 (5 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-20200277305-A1 BET Bromodomain Protein Degraders with Cleavable Linkers BRD4, BET1, BRWD1 CRBN 142/4885IKZF3 453/4885TNF 4467/4885
US-20190263827-A1 FUSED 1,4-DIAZEPINES AS BET PROTEIN DEGRADERS BRD4, BRD1, BET1 CRBN 114/4885IKZF3 206/4885TNF 4719/4885
US-20250073340-A1 SPIROCYCLIC MDM2 MODULATOR AND USES THEREOF FOXM1, MDM2, FOXO1 CRBN 833/4885IKZF3 799/4885TNF 976/4885
US-12569564-B2 Spirocyclic MDM2 modulator and uses thereof MDM2, TP53, XIAP CRBN 39/4885IKZF3 989/4885TNF 2317/4885
US-20250154157-A1 HETEROCYCLIC COMPOUNDS USEFUL FOR TREATING A ERK5-MEDIATED DISEASE MAP3K5, MAPK1, MAP3K20 CRBN 2451/4885IKZF3 3510/4885TNF 2344/4885

“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.