SCHEMBL17859029

SCHEMBL17859029

NCCNC(=O)COc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O

nearest known ligand 0.73

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ CRBN Q96SW2 12/20 0.73
▸ DDB1 Q16531 10/20 0.73
▸ STAT3 P40763 2/20 0.67
▸ HDAC1 Q13547 5/20 0.64
▸ HDAC6 Q9UBN7 5/20 0.64
▸ HDAC3 O15379 2/20 0.64
▸ HDAC2 Q92769 2/20 0.64
▸ HDAC4 P56524 1/20 0.64
▸ NCOR2 Q9Y618 1/20 0.64
▸ TNF P01375 1/20 0.56
▸ IL1B P01584 1/20 0.56
▸ TBXA2R P21731 1/20 0.56
▸ IKZF1 Q13422 1/20 0.56
▸ IKZF3 Q9UKT9 1/20 0.56
▸ MAPT P10636 1/20 0.56
▸ SNCA P37840 1/20 0.56
▸ GSK3B P49841 2/20 0.54

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
SCHEMBL29622145 1.00 CRBN (0.73) CRBNDDB1STAT3HDAC1HDAC6
SCHEMBL23796444 0.95 CRBN (0.70) CRBNDDB1STAT3HDAC1HDAC6
Trifluoroacetic Acid SCHEMBL17839625 0.94 CRBN (0.68) CRBNDDB1STAT3HDAC1HDAC6
SCHEMBL17859033 0.94 STAT3 (0.71) CRBNDDB1STAT3HDAC1HDAC6
SCHEMBL29622126 0.94 STAT3 (0.71) CRBNDDB1STAT3HDAC1HDAC6
Hydrochloric Acid SCHEMBL30893263 0.93 STAT3 (0.70) CRBNDDB1STAT3HDAC1HDAC6
SCHEMBL21070244 0.93 STAT3 (0.70) CRBNDDB1STAT3HDAC1HDAC6
SCHEMBL17859010 0.93 STAT3 (0.70) CRBNDDB1STAT3HDAC1HDAC6
SCHEMBL24142023 0.93 STAT3 (0.70) CRBNDDB1STAT3HDAC1HDAC6
SCHEMBL17859058 0.93 STAT3 (0.70) CRBNDDB1STAT3HDAC1HDAC6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230391765-A1 HETEROBIFUNCTIONAL COMPOUNDS AS DEGRADERS OF ENL ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI 2023-12-07 — — US disclosed
EP-3256470-B1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA FARBER CANCER INST INC (US) 2023-07-26 — — EP disclosed
US-11583586-B2 Methods to induce targeted protein degradation through bifunctional molecules DANA-FARBER CANCER INSTITUTE, INC. (US) 2023-02-21 — — US disclosed
WO-2022086937-A9 HETEROBIFUNCTIONAL COMPOUNDS AS DEGRADERS OF ENL ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (US) 2023-02-02 — — WO disclosed
EP-4119552-A1 REGULATING CHIMERIC ANTIGEN RECEPTORS Dana-Farber Cancer Institute, Inc. (US) 2023-01-18 — — EP disclosed
US-11505560-B2 Heterobifunctional compounds with improved specificity DANA-FARBER CANCER INSTITUTE, INC. (US) 2022-11-22 — — US disclosed
US-20220135967-A1 TUNABLE ENDOGENOUS PROTEIN DEGRADATION DANA-FARBER CANCER INSTITUTE, INC. (US) 2022-05-05 — — US disclosed
WO-2022086937-A1 HETEROBIFUNCTIONAL COMPOUNDS AS DEGRADERS OF ENL ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (US) 2022-04-28 — — WO disclosed
US-11311609-B2 Regulating chimeric antigen receptors DANA-FARBER CANCER INSTITUTE, INC. (US) 2022-04-26 — — US disclosed
US-20210301286-A1 TARGETED PROTEIN DEGRADATION TO ATTENUATE ADOPTIVE T-CELL THERAPY ASSOCIATED ADVERSE INFLAMMATORY RESPONSES DANA-FARBER CANCER INSTITUTE, INC. (US) 2021-09-30 — — US disclosed
US-9694084-B2 Methods to induce targeted protein degradation through bifunctional molecules DANA-FARBER CANCER INSTITUTE, INC. (US) 2017-07-04 — — US disclosed
WO-2017024317-A2 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA-FARBER CANCER INSTITUTE, INC. (US) 2017-02-09 — — WO disclosed
WO-2017024319-A1 TUNABLE ENDOGENOUS PROTEIN DEGRADATION DANA-FARBER CANCER INSTITUTE, INC. (US) 2017-02-09 — — WO disclosed
WO-2017024318-A1 TARGETED PROTEIN DEGRADATION TO ATTENUATE ADOPTIVE T-CELL THERAPY ASSOCIATED ADVERSE INFLAMMATORY RESPONSES DANA-FARBER CANCER INSTITUTE, INC. (US) 2017-02-09 — — WO disclosed
WO-2017007612-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA-FARBER CANCER INSTITUTE, INC. (US) 2017-01-12 — — WO disclosed
US-20160243247-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA-FARBER CANCER INSTITUTE, INC. 2016-08-25 — — US disclosed
US-20160235731-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA-FARBER CANCER INSTITUTE, INC. 2016-08-18 — — US disclosed
US-20160235730-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA-FARBER CANCER INSTITUTE, INC. 2016-08-18 — — US disclosed
WO-2016105518-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA-FARBER CANCER INSTITUTE, INC. (US) 2016-06-30 — — WO disclosed
US-20160176916-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2016-06-23 — — US 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 (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-20160243247-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP CRBN 1/4885DDB1 113/4885STAT3 2989/4885
US-20230391765-A1 HETEROBIFUNCTIONAL COMPOUNDS AS DEGRADERS OF ENL MLLT1, BCR, MCL1 CRBN 11/4885DDB1 668/4885STAT3 1149/4885
US-20210301286-A1 TARGETED PROTEIN DEGRADATION TO ATTENUATE ADOPTIVE T-CELL THERAPY ASSOCIATED ADVERSE INFLAMMATORY RESPONSES NFATC1, GZMB, ICOS CRBN 97/4885DDB1 940/4885STAT3 601/4885
US-11583586-B2 Methods to induce targeted protein degradation through bifunctional molecules CRBN, MDM2, MYCBP CRBN 1/4885DDB1 113/4885STAT3 2989/4885
US-20160235731-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP CRBN 1/4885DDB1 113/4885STAT3 2989/4885
US-20160235730-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP CRBN 1/4885DDB1 113/4885STAT3 2989/4885
US-11311609-B2 Regulating chimeric antigen receptors NFATC1, TNFRSF9, IL2RA CRBN 154/4885DDB1 979/4885STAT3 313/4885
US-11505560-B2 Heterobifunctional compounds with improved specificity MDM2, STUB1, UBE3C CRBN 113/4885DDB1 249/4885STAT3 2082/4885
US-20160176916-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP CRBN 1/4885DDB1 113/4885STAT3 2989/4885
US-20220135967-A1 TUNABLE ENDOGENOUS PROTEIN DEGRADATION PSMG3, MYCBP, DBN1 CRBN 138/4885DDB1 26/4885STAT3 2603/4885

“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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