SCHEMBL986362

SCHEMBL986362

O=C(O)c1cc(Cl)nc(Cl)n1

nearest known ligand 0.51

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
KMO O15229 5/20 0.51
LMNA P02545 2/20 0.50
ALOX15 P16050 2/20 0.48
TSHR P16473 2/20 0.48
HIF1A Q16665 1/20 0.48
GPR35 Q9HC97 2/20 0.47
ALDH1A1 P00352 1/20 0.39
MAPK1 P28482 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
TDP1 Q9NUW8 2/20 0.39
KDM4E B2RXH2 1/20 0.39
ACMSD Q8TDX5 1/20 0.39
S1PR2 O95136 1/20 0.39
MCL1 Q07820 2/20 0.37
KEAP1 Q14145 1/20 0.35
NFE2L2 Q16236 1/20 0.35
TPMT P51580 1/20 0.34

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
Hydrochloric Acid SCHEMBL6525079 0.98 KMO (0.50) KMOLMNAALOX15TSHRHIF1A
Formamide SCHEMBL29197284 0.90 LMNA (0.47) KMOLMNAALOX15TSHRHIF1A
SCHEMBL7878295 0.88 LMNA (0.62) KMOLMNAALOX15TSHRHIF1A
SCHEMBL1179028 0.83 ALDH1A1 (0.55) KMOLMNAALOX15TSHRHIF1A
SCHEMBL5683134 0.82 LMNA (0.50) KMOLMNAALOX15TSHRGPR35
Bicarbonate SCHEMBL10635309 0.80 LMNA (0.46) KMOLMNAALOX15TSHRHIF1A
SCHEMBL113130 0.80 LMNA (0.48) KMOLMNAGPR35ALDH1A1MAPK1
SCHEMBL3659442 0.80 LMNA (0.79) KMOLMNAS1PR2
SCHEMBL15063590 0.78 LMNA (0.52) KMOLMNAALOX15TSHRHIF1A
SCHEMBL9196203 0.78 KMO (0.54) KMOLMNAALOX15TSHRHIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023040830-A1 AHR INHIBITOR, USE THEREOF, AND PREPARATION METHOD THEREFOR 北京华森英诺生物科技有限公司 2023-03-23 WO claimed
US-12612387-B2 RAS inhibitors and methods of using the same JAZZ PHARMACEUTICALS IRELAND LIMITED (IE) 2026-04-28 US disclosed
US-20250382283-A1 COMPOUNDS AND THEIR USES AS CD38 INHIBITORS NANJING IMMUNOPHAGE BIOTECH CO LTD (CN) 2025-12-18 US disclosed
US-20250270201-A1 SUBSTITUTED PYRIMIDINYL HYDRAZIDE COMPOUND AND PREPARATION METHOD AND USE THEREOF ARIGENX THERAPEUTICS CO., LTD. (CN) 2025-08-28 US disclosed
EP-4497747-A1 SUBSTITUTED PYRIMIDINE HYDRAZIDE COMPOUND, METHOD FOR PREPARING SAME, AND USE THEREOF Arigenx Therapeutics Co., Ltd. (CN) 2025-01-29 EP disclosed
US-20240327386-A1 AHR INHIBITOR, USE THEREOF, AND PREPARATION METHOD THEREFOR CHONGQING PHARSCIN INNOBIO CO., LTD. (CN) 2024-10-03 US disclosed
US-20240254113-A1 COMPOUNDS AND THEIR USES AS CD38 INHIBITORS Nanjing Immunophage Biotech Co., Ltd. (CN) 2024-08-01 US disclosed
CN-117715897-A Compounds and their use as CD38 inhibitors 南京艾美斐生物医药科技有限公司 2024-03-15 CN disclosed
CN-117003730-A Substituted pyrimidine hydrazide compound and preparation method and application thereof 德明药泰生物技术(深圳)有限公司 2023-11-07 CN disclosed
WO-2023208018-A1 SUBSTITUTED PYRIMIDINE HYDRAZIDE COMPOUND, METHOD FOR PREPARING SAME, AND USE THEREOF 德明药泰生物技术(深圳)有限公司 2023-11-02 WO disclosed
EP-0996617-B1 2,4-Dithi(oxo)-pyridin-5-yl compounds bearing a tricyclic substituent useful as P2 purinoceptor antagonists ASTRAZENECA AB (SE) 2002-01-09 EP disclosed
EP-1077981-A1 NOVEL CEPHALOSPORIN COMPOUNDS, PROCESSES FOR PREPARATION THEREOF AND ANTIMICROBIAL COMPOSITIONS CONTAINING THE SAME LG CHEMICAL LIMITED (KR) 2001-02-28 EP disclosed
US-6107297-A 2,4-Dithi(oxo)-pyrimidin-5-yl compounds bearing a tricyclic substituent useful as P2 purinoceptor antagonists ASTRA PHARMACEUTICALS LIMITED (GB) 2000-08-22 US disclosed
EP-0996617-A1 NOVEL COMPOUNDS Astra Pharmaceuticals Limited (GB) 2000-05-03 EP disclosed
WO-1999058535-A1 NOVEL CEPHALOSPORIN COMPOUNDS, PROCESSES FOR PREPARATION THEREOF AND ANTIMICROBIAL COMPOSITIONS CONTAINING THE SAME LG CHEMICAL LTD. (KR) 1999-11-18 WO disclosed
WO-1999002501-A1 NOVEL COMPOUNDS ASTRA PHARMACEUTICALS LTD. (GB) 1999-01-21 WO disclosed
US-4534908-A Water-soluble disazo compounds and new bis-(aminophenoxy)-ethane compounds having fiber-reactive groups as the tetrazo components, and use of the disazo compounds as dyestuffs HOECHST AKTIENGESELLSCHAFT (DE) 1985-08-13 US disclosed
EP-0071168-B1 WATER-SOLUBLE DISAZO COMPOUNDS AND BIS-(AMINO-PHENOXY)-ETHANE COMPOUNDS WITH FIBRE REACTIVE GROUPS AS TETRAZO COMPOUNDS, PROCESS FOR THE PREPARATION OF THESE COMPOUNDS AND THE USE OF THE DISAZO COMPOUNDS AS DYESTUFFS HOECHST AKTIENGESELLSCHAFT (DE) 1985-01-30 EP disclosed
US-4394310-A DIAZOTIZATION, CYCLIZATION HOECHST AKTIENGESELLSCHAFT (DE) 1983-07-19 US disclosed
EP-0071168-A2 Water-soluble disazo compounds and bis-(amino-phenoxy)-ethane compounds with fibre reactive groups as tetrazo compounds, process for the preparation of these compounds and the use of the disazo compounds as dyestuffs HOECHST AKTIENGESELLSCHAFT (DE) 1983-02-09 EP 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 (5 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-20240327386-A1 AHR INHIBITOR, USE THEREOF, AND PREPARATION METHOD THEREFOR AHR, ARNT, AIPL1 KMO 372/4885LMNA 3754/4885ALOX15 282/4885
US-20250270201-A1 SUBSTITUTED PYRIMIDINYL HYDRAZIDE COMPOUND AND PREPARATION METHOD AND USE THEREOF AHR, ARNT, PAH KMO 545/4885LMNA 4406/4885ALOX15 1754/4885
US-12612387-B2 RAS inhibitors and methods of using the same KRAS, NRAS, HRAS KMO 4604/4885LMNA 3438/4885ALOX15 3893/4885
US-20240254113-A1 COMPOUNDS AND THEIR USES AS CD38 INHIBITORS CD38, CD22, BCL6B KMO 3914/4885LMNA 518/4885ALOX15 703/4885
US-20250382283-A1 COMPOUNDS AND THEIR USES AS CD38 INHIBITORS CD38, FCGRT, CD22 KMO 2955/4885LMNA 1234/4885ALOX15 801/4885

“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.