SCHEMBL16984550

SCHEMBL16984550

CCOC(=O)c1ccc(Nc2ncc3c(n2)N(C2CCCC2)[C@H](CC)C(=O)N3C)c(OC)c1

nearest known ligand 0.81

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PLK1 P53350 18/20 0.81
PLK3 Q9H4B4 15/20 0.81
PLK2 Q9NYY3 13/20 0.81
PRKD3 O94806 3/20 0.80
CLK2 P49760 3/20 0.80
PTK2 Q05397 3/20 0.80
CAMK2G Q13555 3/20 0.80
CAMK2D Q13557 3/20 0.80
PRKD2 Q9BZL6 3/20 0.80
CSNK1G1 Q9HCP0 3/20 0.80
CSNK1G3 Q9Y6M4 3/20 0.80
MAP4K4 O95819 2/20 0.80
PRKCG P05129 2/20 0.80
RPS6KA3 P51812 2/20 0.80
NEK4 P51957 2/20 0.80
SRPK1 Q96SB4 1/20 0.80
BRD4 O60885 6/20 0.75
ALK Q9UM73 5/20 0.75
BRDT Q58F21 2/20 0.75
DAPK3 O43293 2/20 0.75

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
SCHEMBL29453446 1.00 PLK1 (0.81) PLK1PLK3PLK2PRKD3CLK2
SCHEMBL12825254 0.94 PLK1 (0.84) PLK1PLK3PLK2PRKD3CLK2
SCHEMBL20014306 0.94 PLK1 (0.76) PLK1PLK3PLK2PRKD3CLK2
SCHEMBL16971992 0.91 PLK1 (0.87) PLK1PLK3PLK2PRKD3CLK2
SCHEMBL12323284 0.91 PLK1 (0.85) PLK1PLK3PLK2PRKD3CLK2
SCHEMBL29453442 0.91 PLK1 (0.87) PLK1PLK3PLK2PRKD3CLK2
SCHEMBL376134 0.91 PLK1 (0.87) PLK1PLK3PLK2PRKD3CLK2
SCHEMBL29922386 0.91 PLK1 (0.87) PLK1PLK3PLK2PRKD3CLK2
SCHEMBL15257514 0.91 PLK1 (0.87) PLK1PLK3PLK2PRKD3CLK2
SCHEMBL30325075 0.91 PLK1 (0.86) PLK1PLK3PLK2PRKD3CLK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11583586-B2 Methods to induce targeted protein degradation through bifunctional molecules DANA-FARBER CANCER INSTITUTE, INC. (US) 2023-02-21 US 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-20200317635-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES DANA-FARBER CANCER INSTITUTE, INC. (US) 2020-10-08 US disclosed
US-10669253-B2 Methods to induce targeted protein degradation through bifunctional molecules DANA-FARBER CANCER INSTITUTE, INC. (US) 2020-06-02 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-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-2017024319-A1 TUNABLE ENDOGENOUS PROTEIN DEGRADATION 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-20160347750-A1 DIHYDROPTERIDINONE DERIVATIVES AND USES THEREOF DANA-FARBER CANCER INSTITUTE, INC. (US) 2016-12-01 US 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
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
WO-2015117055-A1 DIHYDROPTERIDINONE DERIVATIVES AND USES THEREOF DANA-FARBER CANCER INSTITUTE, INC. (US) 2015-08-06 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 (15 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 PLK1 838/4885PLK3 3346/4885PLK2 1729/4885
US-20210301286-A1 TARGETED PROTEIN DEGRADATION TO ATTENUATE ADOPTIVE T-CELL THERAPY ASSOCIATED ADVERSE INFLAMMATORY RESPONSES NFATC1, GZMB, ICOS PLK1 2442/4885PLK3 3818/4885PLK2 3917/4885
US-11583586-B2 Methods to induce targeted protein degradation through bifunctional molecules CRBN, MDM2, MYCBP PLK1 838/4885PLK3 3346/4885PLK2 1729/4885
US-11059801-B2 Methods to induce targeted protein degradation through bifunctional molecules CRBN, XIAP, MDM2 PLK1 1307/4885PLK3 3928/4885PLK2 2818/4885
US-20160235731-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP PLK1 838/4885PLK3 3346/4885PLK2 1729/4885
US-11046954-B2 Targeted protein degradation to attenuate adoptive T-cell therapy associated adverse inflammatory responses NFATC1, GZMB, ICOS PLK1 2442/4885PLK3 3818/4885PLK2 3917/4885
US-20210015929-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP PLK1 838/4885PLK3 3346/4885PLK2 1729/4885
US-20160347750-A1 DIHYDROPTERIDINONE DERIVATIVES AND USES THEREOF BRDT, BRD4, BRD3 PLK1 2859/4885PLK3 2255/4885PLK2 2094/4885
US-20160235730-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP PLK1 838/4885PLK3 3346/4885PLK2 1729/4885
US-11311609-B2 Regulating chimeric antigen receptors NFATC1, TNFRSF9, IL2RA PLK1 1768/4885PLK3 4001/4885PLK2 3994/4885
US-10669253-B2 Methods to induce targeted protein degradation through bifunctional molecules CRBN, SMARCE1, MDM2 PLK1 932/4885PLK3 3660/4885PLK2 1995/4885
US-20200317635-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP PLK1 838/4885PLK3 3346/4885PLK2 1729/4885
US-20160176916-A1 METHODS TO INDUCE TARGETED PROTEIN DEGRADATION THROUGH BIFUNCTIONAL MOLECULES CRBN, MDM2, MYCBP PLK1 838/4885PLK3 3346/4885PLK2 1729/4885
US-10849980-B2 Methods to induce targeted protein degradation through bifunctional molecules CRBN, MDM2, MYCBP PLK1 838/4885PLK3 3346/4885PLK2 1729/4885
US-20220135967-A1 TUNABLE ENDOGENOUS PROTEIN DEGRADATION PSMG3, MYCBP, DBN1 PLK1 2709/4885PLK3 4748/4885PLK2 4713/4885

“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.