SCHEMBL15519242

SCHEMBL15519242

CCOC(=O)c1cc(Br)n(C)n1

nearest known ligand 0.46

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.46
LMNA P02545 1/20 0.44
SMN1; SMN2 Q16637 4/20 0.43
NPC1 O15118 3/20 0.43
RAB9A P51151 3/20 0.43
MAPT P10636 3/20 0.43
FAAH O00519 1/20 0.43
GAA P10253 1/20 0.43
KMT2A Q03164 1/20 0.43
ALDH1A1 P00352 1/20 0.43
MMP2 P08253 1/20 0.42
MMP13 P45452 1/20 0.42
MMP14 P50281 1/20 0.42
KDM4E B2RXH2 2/20 0.41
MPO P05164 1/20 0.41
POLB P06746 1/20 0.41
ADORA3 P0DMS8 1/20 0.41

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
SCHEMBL1233517 0.83 BAZ2B (0.54) CYP1A2LMNASMN1; SMN2NPC1RAB9A
SCHEMBL537688 0.81 CYP1A2 (0.47) CYP1A2LMNASMN1; SMN2NPC1RAB9A
SCHEMBL7698241 0.81 LMNA (0.61) CYP1A2LMNASMN1; SMN2NPC1RAB9A
SCHEMBL1314210 0.81 MAPT (0.41) CYP1A2NPC1RAB9AMAPTGAA
SCHEMBL7703560 0.81 MPO (0.47) CYP1A2LMNASMN1; SMN2NPC1RAB9A
SCHEMBL1233249 0.80 MPO (0.49) CYP1A2LMNASMN1; SMN2NPC1RAB9A
SCHEMBL20168414 0.80 CYP1A2 (0.46) CYP1A2LMNASMN1; SMN2NPC1RAB9A
SCHEMBL8003314 0.80 LMNA (0.47) CYP1A2LMNASMN1; SMN2NPC1RAB9A
SCHEMBL1312216 0.80 LMNA (0.50) CYP1A2LMNASMN1; SMN2NPC1RAB9A
SCHEMBL21244231 0.80 CYP1A2 (0.42) CYP1A2SMN1; SMN2NPC1RAB9AMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112079781-B Synthesis method of 5-bromo-1-methyl-1H-pyrazol-3-amine 苏州康润医药有限公司 2022-11-22 CN claimed
CN-112079781-A Synthesis method of 5-bromo-1-methyl-1H-pyrazol-3-amine 苏州康润医药有限公司 2020-12-15 CN claimed
CN-117024411-B Isoquinoline as HPK1 inhibitor 豪夫迈·罗氏有限公司 2026-05-19 CN disclosed
EP-4306529-B1 FGFR INHIBITORS AND METHODS OF USE THEREOF RELAY THERAPEUTICS INC (US) 2026-01-21 EP disclosed
US-12522605-B2 FGFR inhibitors and methods of use thereof RELAY THERAPEUTICS, INC. (US) 2026-01-13 US disclosed
WO-2025111492-A1 INHIBITORS OF PARG 858 THERAPEUTICS, INC. (US) 2025-05-30 WO disclosed
CN-119874707-A FGFR inhibitors and methods of use thereof 传达治疗有限公司 2025-04-25 CN disclosed
CN-114126620-B FGFR inhibitors and methods of use thereof 传达治疗有限公司 2024-12-31 CN disclosed
EP-4306529-A2 FGFR INHIBITORS AND METHODS OF USE THEREOF Relay Therapeutics, Inc. (US) 2024-01-17 EP disclosed
EP-3968999-B1 FGFR INHIBITORS AND METHODS OF USE THEREOF RELAY THERAPEUTICS INC (US) 2023-12-27 EP disclosed
CN-117024411-A Isoquinoline as HPK1 inhibitor 豪夫迈·罗氏有限公司 2023-11-10 CN disclosed
EP-2909212-B1 SUBSTITUTED 1,4-DIHYDROPYRAZOLO[4,3-B]INDOLES TAKEDA PHARMACEUTICALS CO (JP) 2017-02-22 EP disclosed
US-20160332996-A1 Hepatitis B Antiviral Agents ENANTA PHARMACEUTICALS, INC. 2016-11-17 US disclosed
WO-2016183266-A1 EHPATITIS B ANTIVIRAL AGENTS ENANTA PHARMACEUTICALS, INC. (US) 2016-11-17 WO disclosed
US-9475816-B2 Substituted-1,4-dihydropyrazolo[4,3-b]indoles TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2016-10-25 US disclosed
WO-2015197187-A1 PYRAZOLYL-BASED CARBOXAMIDES V Grünenthal GmbH (DE) 2015-12-30 WO disclosed
WO-2015197187-A1 PYRAZOLYL-BASED CARBOXAMIDES V Grünenthal GmbH (DE) 2015-12-30 WO disclosed
EP-2909212-A1 SUBSTITUTED-1,4-DIHYDROPYRAZOLO[4,3-b]INDOLES Takeda Pharmaceutical Company Limited (JP) 2015-08-26 EP disclosed
US-20150225405-A1 SUBSTITUTED-1,4-DIHYDROPYRAZOLO[4,3-b]INDOLES TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2015-08-13 US disclosed
WO-2014039831-A1 SUBSTITUTED-1,4-DIHYDROPYRAZOLO[4,3-b]INDOLES TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2014-03-13 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 (2 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-20150225405-A1 SUBSTITUTED-1,4-DIHYDROPYRAZOLO[4,3-b]INDOLES GPR119, RPLP2, FOXM1 CYP1A2 48/4885LMNA 3139/4885SMN1; SMN2 1529/4885
US-20160332996-A1 Hepatitis B Antiviral Agents ZC3HAV1, ZC3HAV1L, HAVCR2 CYP1A2 541/4885LMNA 345/4885SMN1; SMN2 4775/4885

“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.