SCHEMBL17859010

SCHEMBL17859010

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

nearest known ligand 0.70

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ STAT3 P40763 2/20 0.70
▸ CRBN Q96SW2 9/20 0.69
▸ HDAC1 Q13547 5/20 0.69
▸ HDAC6 Q9UBN7 5/20 0.69
▸ HDAC3 O15379 2/20 0.69
▸ HDAC2 Q92769 2/20 0.69
▸ HDAC4 P56524 1/20 0.69
▸ NCOR2 Q9Y618 1/20 0.69
▸ DDB1 Q16531 7/20 0.68
▸ GSK3B P49841 2/20 0.58
▸ PIP4K2C Q8TBX8 1/20 0.57
▸ TRIM24 O15164 3/20 0.57
▸ BRD4 O60885 4/20 0.56
▸ TRIM33 Q9UPN9 1/20 0.56

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
SCHEMBL21070244 1.00 STAT3 (0.70) STAT3CRBNHDAC1HDAC6HDAC3
SCHEMBL29622083 1.00 STAT3 (0.70) STAT3CRBNHDAC1HDAC6HDAC3
SCHEMBL29622326 1.00 STAT3 (0.70) STAT3CRBNHDAC1HDAC6HDAC3
SCHEMBL29622211 1.00 STAT3 (0.70) STAT3CRBNHDAC1HDAC6HDAC3
SCHEMBL17859058 1.00 STAT3 (0.70) STAT3CRBNHDAC1HDAC6HDAC3
SCHEMBL24142023 1.00 STAT3 (0.70) STAT3CRBNHDAC1HDAC6HDAC3
Hydrochloric Acid SCHEMBL22263309 0.99 STAT3 (0.69) STAT3CRBNHDAC1HDAC6HDAC3
Hydrochloric Acid SCHEMBL22263317 0.99 STAT3 (0.69) STAT3CRBNHDAC1HDAC6HDAC3
Hydrochloric Acid SCHEMBL22263290 0.99 STAT3 (0.69) STAT3CRBNHDAC1HDAC6HDAC3
Hydrochloric Acid SCHEMBL31083322 0.99 STAT3 (0.69) STAT3CRBNHDAC1HDAC6HDAC3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
EP-4119552-A1 REGULATING CHIMERIC ANTIGEN RECEPTORS Dana-Farber Cancer Institute, Inc. (US) 2023-01-18 — — EP disclosed
US-20220135967-A1 TUNABLE ENDOGENOUS PROTEIN DEGRADATION DANA-FARBER CANCER INSTITUTE, INC. (US) 2022-05-05 — — US 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-11059801-B2 Methods to induce targeted protein degradation through bifunctional molecules DANA-FARBER CANCER INSTITUTE, INC. (US) 2021-07-13 — — US disclosed
US-11046954-B2 Targeted protein degradation to attenuate adoptive T-cell therapy associated adverse inflammatory responses DANA-FARBER CANCER INSTITUTE, INC. (US) 2021-06-29 — — US disclosed
US-20210015929-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA-FARBER CANCER INSTITUTE, INC. (US) 2021-01-21 — — US disclosed
US-10849980-B2 Methods to induce targeted protein degradation through bifunctional molecules DANA-FARBER CANCER INSTITUTE, INC. (US) 2020-12-01 — — US disclosed
US-9750816-B2 Methods to induce targeted protein degradation through bifunctional molecules DANA-FARBER CANCER INSTITUTE, INC. (US) 2017-09-05 — — 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-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-20160235730-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA-FARBER CANCER INSTITUTE, INC. 2016-08-18 — — US disclosed
US-20160235731-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 (12 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 STAT3 2989/4885CRBN 1/4885HDAC1 2291/4885
US-20210301286-A1 TARGETED PROTEIN DEGRADATION TO ATTENUATE ADOPTIVE T-CELL THERAPY ASSOCIATED ADVERSE INFLAMMATORY RESPONSES NFATC1, GZMB, ICOS STAT3 601/4885CRBN 97/4885HDAC1 2810/4885
US-11583586-B2 Methods to induce targeted protein degradation through bifunctional molecules CRBN, MDM2, MYCBP STAT3 2989/4885CRBN 1/4885HDAC1 2291/4885
US-11059801-B2 Methods to induce targeted protein degradation through bifunctional molecules CRBN, XIAP, MDM2 STAT3 3234/4885CRBN 1/4885HDAC1 2203/4885
US-20160235731-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP STAT3 2989/4885CRBN 1/4885HDAC1 2291/4885
US-11046954-B2 Targeted protein degradation to attenuate adoptive T-cell therapy associated adverse inflammatory responses NFATC1, GZMB, ICOS STAT3 601/4885CRBN 97/4885HDAC1 2810/4885
US-20210015929-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP STAT3 2989/4885CRBN 1/4885HDAC1 2291/4885
US-20160235730-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP STAT3 2989/4885CRBN 1/4885HDAC1 2291/4885
US-11311609-B2 Regulating chimeric antigen receptors NFATC1, TNFRSF9, IL2RA STAT3 313/4885CRBN 154/4885HDAC1 2500/4885
US-20160176916-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP STAT3 2989/4885CRBN 1/4885HDAC1 2291/4885
US-10849980-B2 Methods to induce targeted protein degradation through bifunctional molecules CRBN, MDM2, MYCBP STAT3 2989/4885CRBN 1/4885HDAC1 2291/4885
US-20220135967-A1 TUNABLE ENDOGENOUS PROTEIN DEGRADATION PSMG3, MYCBP, DBN1 STAT3 2603/4885CRBN 138/4885HDAC1 4152/4885

“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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