SCHEMBL856815

SCHEMBL856815

Clc1cc(N2CCOCC2)nc(Cl)n1

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.70
CYP1A2 P05177 1/20 0.70
CYP2D6 P10635 1/20 0.70
KMT2A Q03164 4/20 0.64
RAF1 P04049 1/20 0.51
BRAF P15056 1/20 0.51
HTT P42858 1/20 0.47
CRHBP P24387 1/20 0.47
CRHR2 Q13324 1/20 0.47
MEN1 O00255 2/20 0.47
NPC1 O15118 1/20 0.47
RAB9A P51151 1/20 0.47
POLB P06746 1/20 0.45
NPSR1 Q6W5P4 2/20 0.44
TSHR P16473 1/20 0.44
MAPK1 P28482 1/20 0.44
HSD17B10 Q99714 1/20 0.44
SMN1; SMN2 Q16637 2/20 0.43
HRH4 Q9H3N8 1/20 0.43
KDM4E B2RXH2 1/20 0.43

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
SCHEMBL29762330 1.00 MAPT (0.70) MAPTCYP1A2CYP2D6KMT2ARAF1
SCHEMBL856718 0.90 MAPT (0.61) MAPTCYP1A2CYP2D6KMT2ARAF1
SCHEMBL21158324 0.89 MAPT (0.57) MAPTCYP1A2CYP2D6KMT2ARAF1
SCHEMBL855348 0.84 MAPT (0.68) MAPTCYP1A2CYP2D6KMT2ARAF1
SCHEMBL17859942 0.83 CYP1A2 (0.54) MAPTCYP1A2CYP2D6KMT2ARAF1
SCHEMBL1748520 0.82 CYP1A2 (0.47) MAPTCYP1A2CYP2D6KMT2ACRHBP
SCHEMBL2771738 0.82 CYP1A2 (0.47) MAPTCYP1A2CYP2D6KMT2ACRHBP
SCHEMBL13989245 0.82 MAPT (0.66) MAPTCYP1A2CYP2D6KMT2ARAF1
SCHEMBL1028538 0.82 CYP1A2 (1.00) MAPTCYP1A2CYP2D6KMT2ARAF1
SCHEMBL30353341 0.82 CYP1A2 (0.66) MAPTCYP1A2CYP2D6KMT2ARAF1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113683596-B Pyrimidine tankyrase 2 inhibitor and preparation method and application thereof 上海应用技术大学 2023-02-10 CN claimed
CN-113683596-A Pyrimidine tankyrase 2 inhibitor and preparation method and application thereof 上海应用技术大学 2021-11-23 CN claimed
EP-4696326-A1 PIKFYVE PROTEIN KINASE DEGRADATION AGENT AND USE THEREOF SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY, CHINESE ACADEMY OF SCIENCES (CN) 2026-02-18 EP disclosed
US-12497407-B2 Treatment of skin disorders TORQUR AG (CH) 2025-12-16 US disclosed
US-12312336-B2 Inhibitors of RAF kinases Pierre Fabre Médicament (FR) 2025-05-27 US disclosed
US-20240382496-A1 TREATMENT OF SKIN LESIONS TORQUR AG (CH) 2024-11-21 US disclosed
US-20240368184-A1 PIKfyve Inhibitors MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2024-11-07 US disclosed
US-20240343718-A1 TREATMENT OF NEUROLOGICAL DISORDERS TORQUR AG (CH) 2024-10-17 US disclosed
WO-2024213160-A1 PIKFYVE PROTEIN KINASE DEGRADATION AGENT AND USE THEREOF 中国科学院上海有机化学研究所 2024-10-17 WO disclosed
US-12030896-B2 PIKfyve inhibitors MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2024-07-09 US disclosed
US-12030896-B2 PIKfyve inhibitors MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2024-07-09 US disclosed
WO-2005007646-A1 SUBSTITUTED HETEROCYCLIC DIARYLAMINE ANALOGUES NEUROGEN CORPORATION (US) 2005-01-27 WO disclosed
WO-2005000404-A2 HETEROCYCLIC COMPOUNDS FOR PREVENTING AND TREATING DISORDERS ASSOCIATED WITH EXCESSIVE BONE LOSS SYNTA PHARMACEUTICALS, CORP. (US) 2005-01-06 WO disclosed
EP-1458687-A2 PYRIMIDINE COMPOUNDS Synta Pharmaceuticals Corporation (US) 2004-09-22 EP disclosed
WO-2004024810-A2 STABILLIZATION OF ORGANIC MATERIALS CIBA, SPECIALTY CHEMICALS HOLDING INC. (CH) 2004-03-25 WO disclosed
US-20040048873-A1 Pyrimidine compounds SYNTA PHARMACEUTICALS CORP., A DELAWARE CORPORATIO 2004-03-11 US disclosed
US-6693097-B2 Pyrimidine compounds SYNTA PHARMACEUTICALS CORP. 2004-02-17 US disclosed
US-20040024206-A1 Pyrimidine compounds MADRIGAL PHARMACEUTICALS, INC. 2004-02-05 US disclosed
US-20030139403-A1 Pyrimidine compounds SHIONOGI BIORESEARCH CORP. 2003-07-24 US disclosed
WO-2003047516-A2 PYRIMIDINE COMPOUNDS SYNTA PHARMACEUTICALS CORPORATION (US) 2003-06-12 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 (9 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-12030896-B2 PIKfyve inhibitors PIKFYVE, PIP4K2B, PIP4K2A MAPT 3914/4885CYP1A2 3815/4885CYP2D6 3982/4885
US-20240382496-A1 TREATMENT OF SKIN LESIONS C1R, C3AR1, CXCR3 MAPT 2395/4885CYP1A2 303/4885CYP2D6 348/4885
US-20240343718-A1 TREATMENT OF NEUROLOGICAL DISORDERS CHRM2, CHRM1, C1R MAPT 261/4885CYP1A2 136/4885CYP2D6 146/4885
US-20240368184-A1 PIKfyve Inhibitors PIKFYVE, PIP4K2B, PIP4K2A MAPT 3914/4885CYP1A2 3815/4885CYP2D6 3982/4885
US-12497407-B2 Treatment of skin disorders RXFP3, CCR3, CBR3 MAPT 2061/4885CYP1A2 405/4885CYP2D6 638/4885
US-20030139403-A1 Pyrimidine compounds CBR1, CBR3, CCNO MAPT 4042/4885CYP1A2 579/4885CYP2D6 171/4885
US-20040024206-A1 Pyrimidine compounds CBR1, CCR4, CNR1 MAPT 2986/4885CYP1A2 469/4885CYP2D6 245/4885
US-12312336-B2 Inhibitors of RAF kinases BRAF, RAF1, ARAF MAPT 2859/4885CYP1A2 4302/4885CYP2D6 4339/4885
US-20040048873-A1 Pyrimidine compounds CBR1, CBR3, CCNO MAPT 4185/4885CYP1A2 684/4885CYP2D6 207/4885

“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.