SCHEMBL2591086

SCHEMBL2591086

Cc1c(C(=O)O)cc(Br)cc1[N+](=O)[O-]

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.56
GPR35 Q9HC97 1/20 0.51
CYP1A2 P05177 1/20 0.47
HSD17B10 Q99714 1/20 0.45
DTYMK P23919 1/20 0.42
ERN1 O75460 1/20 0.42
AKR1C2 P52895 2/20 0.42
AKR1C1 Q04828 2/20 0.42
AKR1C4 P17516 1/20 0.42
AKR1C3 P42330 1/20 0.42
FBP1 P09467 1/20 0.41
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
ALDH1A1 P00352 1/20 0.40
MAPT P10636 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
TPMT P51580 1/20 0.40
PKM P14618 1/20 0.40
CASP6 P55212 1/20 0.40

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
SCHEMBL31062952 1.00 TSHR (0.56) TSHRGPR35CYP1A2HSD17B10DTYMK
SCHEMBL13468174 0.86 CYP1A2 (0.47) TSHRGPR35CYP1A2ERN1MEN1
SCHEMBL23985882 0.85 CYP1A2 (0.46) TSHRGPR35CYP1A2ERN1MEN1
SCHEMBL3939940 0.83 PDGFRB (0.49) TSHRGPR35CYP1A2ERN1MEN1
SCHEMBL7055312 0.82 GPR35 (0.54) TSHRGPR35HSD17B10DTYMKERN1
SCHEMBL6830067 0.82 TSHR (0.59) TSHRGPR35CYP1A2DTYMKMEN1
SCHEMBL31218395 0.82 HSD17B10 (0.61) TSHRGPR35HSD17B10DTYMKERN1
SCHEMBL1708885 0.82 HSD17B10 (0.61) TSHRGPR35HSD17B10DTYMKERN1
SCHEMBL5201165 0.81 CYP1A2 (0.61) TSHRGPR35CYP1A2HSD17B10ERN1
SCHEMBL1446831 0.81 AKR1C2 (0.56) TSHRGPR35CYP1A2HSD17B10DTYMK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118406041-A Tazemetostat synthesis method 沈阳药科大学 2024-07-30 CN claimed
CN-116655612-A Synthetic method and application of EZH2 inhibitor 王亚男 2023-08-29 CN claimed
CN-113527275-A SKLB1039 compound and preparation method and application thereof 成都师范学院 2021-10-22 CN claimed
EP-2877462-A1 PROCESSES FOR PREPARING ISOINDOLINE-1,3-DIONE COMPOUNDS Celgene Corporation (US) 2015-06-03 EP claimed
WO-2014018866-A1 PROCESSES FOR PREPARING ISOINDOLINE-1,3-DIONE COMPOUNDS CELGENE CORPORATION (US) 2014-01-30 WO claimed
US-20140031552-A1 PROCESSES FOR PREPARING ISOINDOLINE-1,3-DIONE COMPOUNDS CELGENE CORPORATION (US) 2014-01-30 US claimed
CN-122010899-A Continuous flow preparation method of lenalidomide and derivatives thereof 深圳连续制药科技有限公司 2026-05-12 CN disclosed
US-12577255-B2 MDM2-based modulators of proteolysis and associated methods of use ARVINAS OPERATIONS, INC. (US) 2026-03-17 US disclosed
US-12581252-B2 Substituted pyrrolo[3,4-b]pyridines as PI3K-α inhibitors RELAY THERAPEUTICS, INC. (US) 2026-03-17 US disclosed
US-20250268905-A1 SALT FORM OF A HUMAN HISTONE METHYLTRANSFERASE EZH2 INHIBITOR EISAI R&D MANAGEMENT CO., LTD. (JP) 2025-08-28 US disclosed
US-20250170138-A1 ARYL-OR HETEROARYL-SUBSTITUTED BENZENE COMPOUNDS Epizyme, Inc. 2025-05-29 US disclosed
US-20250109123-A1 COMBINATION THERAPY FOR TREATING CANCER Epizyme, Inc. 2025-04-03 US disclosed
US-12251386-B2 Salt form of a human histone methyltransferase EZH2 inhibitor Epizyme, Inc. (US) 2025-03-18 US disclosed
WO-2005084315-A2 PYRANOINDOLE DERIVATIVES AND THE USE THEREOF FOR THE TREATMENT OF HEPATITIS C VIRUS INFECTION OR DISEASE VIROPHARMA INCORPORATED (US) 2005-09-15 WO disclosed
CN-1655778-A Methods of treating hepatitis C virus infection using pyranoindole derivatives WYETH CORP (US) 2005-08-17 CN disclosed
EP-1509225-A1 METHOD FOR THE USE OF PYRANOINDOLE DERIVATIVES TO TREAT INFECTION WITH HEPATITIS C VIRUS Wyeth (US) 2005-03-02 EP disclosed
US-20040082643-A1 Method for the use of pyranoindole derivatives to treat infection with Hepatitis C virus WYETH (US) 2004-04-29 US disclosed
WO-2003099275-A1 METHOD FOR THE USE OF PYRANOINDOLE DERIVATIVES TO TREAT INFECTION WITH HEPATITIS C VIRUS WYETH (US) 2003-12-04 WO disclosed
EP-0266349-A1 TRICYCLIC INDOLE DERIVATIVES, THEIR MANUFACTURE AND USE AS MEDICINES. SCHERING AG (DE) 1988-05-11 EP disclosed
WO-1987000522-A1 TRICYCLIC INDOLE DERIVATIVES, THEIR MANUFACTURE AND USE AS MEDICINES SCHERING AKTIENGESELLSCHAFT BERLIN UND BERGKAMEN (DE) 1987-01-29 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 (8 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-20040082643-A1 Method for the use of pyranoindole derivatives to treat infection with Hepatitis C virus HAVCR2, HCCS, ZC3HAV1 TSHR 384/4885GPR35 2617/4885CYP1A2 19/4885
US-12577255-B2 MDM2-based modulators of proteolysis and associated methods of use MDM2, UBR4, UBE3A TSHR 1436/4885GPR35 4560/4885CYP1A2 4406/4885
US-20250170138-A1 ARYL-OR HETEROARYL-SUBSTITUTED BENZENE COMPOUNDS AHR, ARNT, CYP1B1 TSHR 3819/4885GPR35 779/4885CYP1A2 15/4885
US-20140031552-A1 PROCESSES FOR PREPARING ISOINDOLINE-1,3-DIONE COMPOUNDS UGT1A1, CYP3A5, CYP3A7 TSHR 4230/4885GPR35 3144/4885CYP1A2 9/4885
US-20250109123-A1 COMBINATION THERAPY FOR TREATING CANCER EZH2, BMI1, HDAC2 TSHR 3874/4885GPR35 3499/4885CYP1A2 4431/4885
US-12251386-B2 Salt form of a human histone methyltransferase EZH2 inhibitor EZH2, DOT1L, NSD1 TSHR 3985/4885GPR35 4374/4885CYP1A2 4333/4885
US-12581252-B2 Substituted pyrrolo[3,4-b]pyridines as PI3K-α inhibitors RORB, ROR1, RORA TSHR 146/4885GPR35 1736/4885CYP1A2 986/4885
US-20250268905-A1 SALT FORM OF A HUMAN HISTONE METHYLTRANSFERASE EZH2 INHIBITOR EZH2, DOT1L, NSD1 TSHR 3985/4885GPR35 4374/4885CYP1A2 4333/4885

“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.