SCHEMBL7785654

SCHEMBL7785654

CNC(=O)Nc1cccnc1

nearest known ligand 0.68

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 5/20 0.68
NPC1 O15118 5/20 0.68
MEN1 O00255 4/20 0.63
KMT2A Q03164 4/20 0.63
ALDH1A1 P00352 2/20 0.62
HTT P42858 2/20 0.62
KDM4E B2RXH2 1/20 0.62
LMNA P02545 3/20 0.61
MAPT P10636 3/20 0.61
CDK2 P24941 1/20 0.61
FLT4 P35916 1/20 0.61
PKM P14618 2/20 0.61
TSHR P16473 1/20 0.59
TAAR1 Q96RJ0 1/20 0.59
ATM Q13315 1/20 0.59
HIF1A Q16665 1/20 0.59
L3MBTL1 Q9Y468 1/20 0.58
AHR P35869 1/20 0.57
CYP1A2 P05177 1/20 0.57

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
SCHEMBL30633570 1.00 RAB9A (0.68) RAB9ANPC1MEN1KMT2AALDH1A1
SCHEMBL9637653 0.88 MEN1 (0.77) RAB9ANPC1MEN1KMT2AALDH1A1
SCHEMBL30051982 0.88 MEN1 (0.77) RAB9ANPC1MEN1KMT2AALDH1A1
Bromide SCHEMBL29417998 0.86 MEN1 (0.74) RAB9ANPC1MEN1KMT2AALDH1A1
Hydrochloric Acid SCHEMBL29388210 0.86 MEN1 (0.74) RAB9ANPC1MEN1KMT2AALDH1A1
SCHEMBL12120402 0.86 RAB9A (0.64) RAB9ANPC1MEN1KMT2AALDH1A1
SCHEMBL10756618 0.84 RAB9A (0.54) RAB9ANPC1MEN1KMT2AALDH1A1
SCHEMBL10857079 0.84 RAB9A (0.57) RAB9ANPC1MEN1KMT2AALDH1A1
SCHEMBL10665495 0.83 RAB9A (0.79) RAB9ANPC1MEN1KMT2AALDH1A1
SCHEMBL5633303 0.81 RAB9A (0.63) RAB9ANPC1MEN1KMT2AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101022810-A Novel biaromatic compounds which activate peroxisome proliferator activated receptor-like receptors and their use in cosmetic or pharmaceutical compositions GALDERMA RES & DEV (FR) 2007-08-22 CN claimed
US-4959092-A Substituted phenyl (or pyridyl) urea compound and herbicidal composition containing the same as active ingredient MITSUBISHI KASEI CORPORATION (JP) 1990-09-25 US claimed
EP-0293839-A2 Substituted phenyl (or pyridyl) urea compound and herbicidal composition containing the same as active ingredient MITSUBISHI KASEI CORPORATION (JP) 1988-12-07 EP claimed
JP-1157981-A None JP disclosed
WO-2023171783-A1 PYRAZOLE COMPOUND, AND NOXIOUS ORGANISM CONTROL AGENT CONTAINING SAME AS ACTIVE INGREDIENT 三井化学アグロ株式会社 2023-09-14 WO disclosed
US-20230219979-A1 PYRAZOLO[1,5-a]PYRIDINE COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF SHENZHEN ZHONGGE BIOLOGICAL TECHNOLOGY CO., LTD. (CN) 2023-07-13 US disclosed
WO-2022261524-A1 HETEROARYL COMPOUNDS AS INHIBITORS OF TYK2, COMPOSITION AND APPLICATION THEREOF ACCRO BIOSCIENCE (HK) LIMITED (CN) 2022-12-15 WO disclosed
EP-4074710-A1 PYRAZOLO[1,5-A]PYRIDINE COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF Shenzhen Zhongge Biological Technology Co., Ltd (CN) 2022-10-19 EP disclosed
CN-114787161-A Pyrazolo [1,5-a ] pyridine compound and preparation method and application thereof 深圳众格生物科技有限公司 2022-07-22 CN disclosed
US-10351522-B2 Sulfonamide derivative and pharmaceutically acceptable acid addition salt thereof UNIVERSITY OF TSUKUBA (JP) 2019-07-16 US disclosed
US-10017481-B2 Conformationally constrained, fully synthetic macrocyclic compounds POLYPHOR AG (CH) 2018-07-10 US disclosed
WO-2008006563-A1 PURINE DERIVATIVES AS A2A AGONISTS NOVARTIS AG (CH) 2008-01-17 WO disclosed
EP-1147079-A2 BETA-PHENYLALANINE DERIVATIVES AS INTEGRIN ANTAGONISTS Bayer Aktiengesellschaft (DE) 2001-10-24 EP disclosed
WO-2000041469-A2 β-PHENYLALANINE DERIVATIVES AS INTEGRIN ANTAGONISTS BAYER AKTIENGESELLSCHAFT (DE) 2000-07-20 WO disclosed
US-4959092-A Substituted phenyl (or pyridyl) urea compound and herbicidal composition containing the same as active ingredient MITSUBISHI KASEI CORPORATION (JP) 1990-09-25 US disclosed
JP-H01157981-A SUBSTITUTED PYRIDYLUREA DERIVATIVE AND HERBICIDE COMPRISING SAID DERIVATIVE AS ACTIVE INGREDIENT MITSUBISHI KASEI CORP 1989-06-21 JP disclosed
US-4824955-A ANTITUMOR AGENTS NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1989-04-25 US disclosed
EP-0293839-A2 Substituted phenyl (or pyridyl) urea compound and herbicidal composition containing the same as active ingredient MITSUBISHI KASEI CORPORATION (JP) 1988-12-07 EP disclosed
EP-0222414-A2 Novel organic selenium compounds NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1987-05-20 EP disclosed
US-4334912-A HERBICIDES WHICH ARE NONPHYTOTOXIC TO CROPS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1982-06-15 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 (3 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-20230219979-A1 PYRAZOLO[1,5-a]PYRIDINE COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF RET, GRK4, RIN1 RAB9A 217/4885NPC1 1928/4885MEN1 830/4885
US-10351522-B2 Sulfonamide derivative and pharmaceutically acceptable acid addition salt thereof HCRTR2, HCRTR1, NPSR1 RAB9A 2688/4885NPC1 733/4885MEN1 2469/4885
US-10017481-B2 Conformationally constrained, fully synthetic macrocyclic compounds CTSE, CTSB, CTSS RAB9A 2677/4885NPC1 3288/4885MEN1 1674/4885

“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.