SCHEMBL266855

SCHEMBL266855

Cc1n[nH]c2ccc(N)cc12

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GSK3B P49841 1/20 0.56
AXL P30530 3/20 0.50
JAK2 O60674 5/20 0.47
ADORA2A P29274 1/20 0.46
ADORA2B P29275 1/20 0.46
HTR2A P28223 1/20 0.45
HTR2C P28335 1/20 0.45
HTR2B P41595 1/20 0.45
PDPK1 O15530 3/20 0.44
CYP1A2 P05177 1/20 0.43
IMPDH2 P12268 1/20 0.42
AURKA O14965 1/20 0.42
KDM4E B2RXH2 2/20 0.41
GAA P10253 2/20 0.41
MEN1 O00255 1/20 0.41
ROCK2 O75116 1/20 0.41
ALDH1A1 P00352 1/20 0.41
MAPT P10636 1/20 0.41
HPGD P15428 1/20 0.41
RAB9A P51151 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
SCHEMBL29644057 1.00 GSK3B (0.56) GSK3BAXLJAK2ADORA2AADORA2B
SCHEMBL29613696 0.84 AXL (0.50) GSK3BAXLJAK2ADORA2AADORA2B
SCHEMBL588513 0.84 AXL (0.50) GSK3BAXLJAK2ADORA2AADORA2B
Hydrochloric Acid SCHEMBL588415 0.82 AXL (0.49) GSK3BAXLJAK2ADORA2AADORA2B
SCHEMBL118573 0.81 JAK2 (0.64) GSK3BAXLJAK2HTR2AHTR2C
SCHEMBL12193658 0.79 MKNK1 (0.61) GSK3BAXLJAK2HTR2AHTR2C
SCHEMBL29769133 0.79 MAP2K4 (0.57) JAK2ADORA2AADORA2BCYP1A2KDM4E
SCHEMBL12222 0.79 MAP2K4 (0.57) JAK2ADORA2AADORA2BCYP1A2KDM4E
Hydrazine SCHEMBL5316054 0.77 JAK2 (0.65) GSK3BAXLJAK2ADORA2AADORA2B
SCHEMBL4222590 0.77 AXL (0.55) GSK3BAXLHTR2AHTR2CHTR2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118027006-A 2, 4-Diaminopyrimidine derivative and preparation method and application thereof 温州医科大学附属第一医院 2024-05-14 CN claimed
CN-102658057-B Novel polyurethane dispersant and preparation method thereof WANG ZHIJUN 2014-09-10 CN claimed
CN-102658057-A Novel polyurethane dispersant and preparation method thereof ZHIJUN WANG 2012-09-12 CN claimed
EP-0904769-B1 Keratin fibre dye compositions containing Indazole amine derivatives and dyeing method OREAL (FR) 2002-09-25 EP claimed
EP-0904769-A1 Keratin fibre dye compositions containing Indazole amine derivatives and dyeing method L'OREAL (FR) 1999-03-31 EP claimed
EP-4724443-A1 PYRAZOLO-PYRIMIDINONE COMPOUNDS FOR USE IN METHODS OF INHIBITING WEE1 A KINASE Acrivon Therapeutics, Inc. (US) 2026-04-15 EP disclosed
US-12338226-B2 Substituted benzodiazoles and use thereof in therapy THOMAS HELLEDAYS STIFTELSE FOR MEDICINSK FORSKNING (SE) 2025-06-24 US disclosed
WO-2025129167-A1 INHIBITORS OF THE SURFACE EXPRESSION OF THE VOLTAGE-GATED SODIUM ION CHANNEL 1.7 (NAV1.7) AND THEIR THERAPEUTIC USES THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPT. OF HEALTH AND HUMAN SERVICES (US) 2025-06-19 WO disclosed
EP-3676255-B1 THERAPEUTIC INDAZOLES RUTGERS THE STATE UNIV UNIV OF NEW JERSEY (US) 2025-04-16 EP disclosed
EP-4476208-A1 GLP-1R MODULATING COMPOUNDS Ascletis Bioscience Co., Ltd. (CN) 2024-12-18 EP disclosed
WO-2024254490-A1 PYRAZOLO-PYRIMIDINONE COMPOUNDS FOR USE IN METHODS OF INHIBITING WEE1 A KINASE ACRIVON THERAPEUTICS, INC. (US) 2024-12-12 WO disclosed
CN-118984827-A GLP-1R modulating compounds 歌礼生物科技(杭州)有限公司 2024-11-19 CN disclosed
EP-1403255-A1 Rho KINASE INHIBITORS SUMITOMO PHARMACEUTICALS COMPANY, LIMITED (JP) 2004-03-31 EP disclosed
US-20040014755-A1 Rho-kinase inhibitors BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2004-01-22 US disclosed
WO-2003063794-A2 2,4-PYRIMIDINEDIAMINE COMPOUNDS AND THEIR USES RIGEL PHARMACEUTICALS, INC. (US) 2003-08-07 WO disclosed
WO-2003059913-A1 ROH-KINASE INHIBITORS BAYER HEALTHCARE AG (DE) 2003-07-24 WO disclosed
EP-0904769-B1 Keratin fibre dye compositions containing Indazole amine derivatives and dyeing method OREAL (FR) 2002-09-25 EP disclosed
US-6027538-A OXIDATION DYEING OF KERATINOUS FIBERS CONTAINING AT LEAST ONE COUPLER SELECTED FROM INDAZOLEAMINE DERIVATIVES AND AT LEAST ONE OXIDATION BASE; POWERFUL, NOT VERY SELECTIVE HAIR DYES WHICH ARE CAPABLE OF GENERATING INTENSE COLOR L'OREAL S.A. (FR) 2000-02-22 US disclosed
EP-0904769-A1 Keratin fibre dye compositions containing Indazole amine derivatives and dyeing method L'OREAL (FR) 1999-03-31 EP disclosed
WO-1994014801-A1 HETEROCYCLIC UREA DERIVATIVES AS 5HT2C AND 5HT2B ANTAGONISTS SMITHKLINE BEECHAM PLC (GB) 1994-07-07 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-20040014755-A1 Rho-kinase inhibitors CIT, ROCK1, ROCK2 GSK3B 312/4885AXL 2691/4885JAK2 1191/4885
US-12338226-B2 Substituted benzodiazoles and use thereof in therapy XDH, CYP11B2, CYP4X1 GSK3B 2546/4885AXL 2740/4885JAK2 7/4885

“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.