SCHEMBL275155

SCHEMBL275155

O=Cc1c(Cl)ncnc1Cl

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.40
ALDH1A1 P00352 2/20 0.40
MEN1 O00255 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
AXL P30530 1/20 0.37
MKNK1 Q9BUB5 1/20 0.37
MKNK2 Q9HBH9 1/20 0.37
NFE2L2 Q16236 1/20 0.35
PDE4A P27815 1/20 0.34
PDE4B Q07343 1/20 0.34
PDE4C Q08493 1/20 0.34
PDE4D Q08499 1/20 0.34
KDM4E B2RXH2 2/20 0.32
MAPT P10636 2/20 0.32
NPSR1 Q6W5P4 2/20 0.32
DYRK1A Q13627 1/20 0.32
LMNA P02545 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31
HTT P42858 1/20 0.31
HSD17B10 Q99714 1/20 0.31

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
SCHEMBL6066165 0.97 KMT2A (0.39) KMT2AALDH1A1MEN1TDP1AXL
Phosphine SCHEMBL6066159 0.97 KMT2A (0.39) KMT2AALDH1A1MEN1TDP1AXL
Hydrazine SCHEMBL5282146 0.95 KMT2A (0.37) KMT2AALDH1A1MEN1TDP1AXL
SCHEMBL16019052 0.84 MEN1 (0.33) KMT2AALDH1A1MEN1TDP1NFE2L2
SCHEMBL13946887 0.84 ALDH1A1 (0.34) KMT2AALDH1A1MEN1TDP1NFE2L2
SCHEMBL678617 0.84 EGFR (0.36) KMT2AALDH1A1MEN1TDP1NFE2L2
SCHEMBL6066125 0.83 MEN1 (0.38) KMT2AALDH1A1MEN1TDP1KDM4E
SCHEMBL8582433 0.79 MEN1 (0.30) KMT2AALDH1A1MEN1TDP1
SCHEMBL6718662 0.79 ALDH1A1 (0.42) KMT2AALDH1A1MEN1NFE2L2MAPT
SCHEMBL1094509 0.79 PDPK1 (0.34) KMT2AALDH1A1MEN1TDP1NFE2L2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119431491-A Synthesis method of Fmoc-Xaa-Ser (Psi (Me, me) Pro) -OH pseudo dipeptide 杭州湃肽生化科技有限公司 2025-02-14 CN claimed
CN-118440010-A Preparation method of 4, 6-dichloro-5-pyrimidine acetaldehyde 诚达药业股份有限公司 2024-08-06 CN claimed
CN-117110483-A Liquid chromatographic analysis and detection method for 5-pyrimidine formaldehyde compounds 常州合全药业有限公司 2023-11-24 CN claimed
CN-106311176-A Particle adsorption agent for indole adsorption and preparation method thereof 北京益净环保设备科技有限公司 2017-01-11 CN claimed
CN-106311178-A Functional plate for indole adsorption and preparation method thereof 北京益净环保设备科技有限公司 2017-01-11 CN claimed
CN-106268698-A Feature board for Adsorption of Pyridine and preparation method thereof 北京益净环保设备科技有限公司 2017-01-04 CN claimed
CN-106268697-A Granule adsorbent for Adsorption of Pyridine and preparation method thereof 北京益净环保设备科技有限公司 2017-01-04 CN claimed
CN-105622613-A Method for synthesizing ibrutinib AOPUTON (SHANGHAI) MEDICAL TECH CO LTD 2016-06-01 CN claimed
CN-103058935-B Pyrimidine compound as well as preparation method and use for same UNIV SICHUAN 2015-05-06 CN claimed
CN-102180880-B Method for synthesizing bromophenyl pyrazolo[3,4-d]pyrimidine derivative UNIV CHANGZHOU 2014-04-09 CN claimed
CN-103058935-A Pyrimidine compound as well as preparation method and use for same UNIV SICHUAN 2013-04-24 CN claimed
CN-102115475-B Method for synthesizing pyrazolo[3,4-d]pyrimidine derivative by two steps UNIV CHANGZHOU 2013-01-16 CN claimed
EP-0506628-B1 Aminoacyl and oligopeptidyl derivatives of allopurinol exhibiting immunostimulatory activity, and pharmaceutical formulations containing these substances SIGMA TAU IND FARMACEUTI (IT) 1996-09-18 EP claimed
US-4380629-A Styryl-like compounds showing a color-developing and bleaching behavior with improved stability and prolonged lifetime MATSUSHITA ELECTRIC INDUSTRIAL COMPANY, LIMITED (JP) 1983-04-19 US claimed
US-4314058-A Indolins styryl-like compounds MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 1982-02-02 US claimed
US-4147862-A Method of preparing styryl-like compounds MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 1979-04-03 US claimed
EP-4747260-A1 MACROCYCLES FOR THE TREATMENT OF AUTOIMMUNE DISEASE F. Hoffmann-La Roche AG (CH) 2026-05-27 EP disclosed
US-20260132133-A1 MACROCYCLIC HETEROCYCLES AND USES THEREOF KUMQUAT BIOSCIENCES INC (US) 2026-05-14 US disclosed
US-4100286-A 2-(Substituted heterocyclic amine)benzoic acids SCIENCE UNION ET CIE (FR) 1978-07-11 US disclosed
US-4003633-A Color display device MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JA) 1977-01-18 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 (1 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-20260132133-A1 MACROCYCLIC HETEROCYCLES AND USES THEREOF KRAS, HRAS, BCL6 KMT2A 4453/4885ALDH1A1 3584/4885MEN1 3010/4885

“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.