SCHEMBL240423

SCHEMBL240423

Clc1ccc(-c2ccccc2)nn1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 4/20 0.50
NPC1 O15118 3/20 0.50
SMN1; SMN2 Q16637 2/20 0.50
USP2 O75604 1/20 0.50
TP53 P04637 1/20 0.50
PKM P14618 1/20 0.50
ALDH1A1 P00352 3/20 0.46
MEN1 O00255 3/20 0.46
KMT2A Q03164 3/20 0.46
HPGD P15428 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46
HTT P42858 1/20 0.46
KDM4E B2RXH2 2/20 0.44
HSD17B10 Q99714 1/20 0.44
HSP90AA1 P07900 1/20 0.44
HSP90AB1 P08238 1/20 0.44
LMNA P02545 1/20 0.43
SMARCA2 P51531 1/20 0.42
SMARCA4 P51532 1/20 0.42
PBRM1 Q86U86 1/20 0.42

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
SCHEMBL30402035 1.00 RAB9A (0.50) RAB9ANPC1SMN1; SMN2USP2TP53
SCHEMBL13458074 0.96 SMN1; SMN2 (0.47) RAB9ANPC1SMN1; SMN2USP2TP53
SCHEMBL10803637 0.92 SMN1; SMN2 (0.44) RAB9ANPC1SMN1; SMN2USP2TP53
SCHEMBL2493590 0.84 RAB9A (0.62) RAB9ANPC1SMN1; SMN2USP2TP53
SCHEMBL23731087 0.81 CYP1A2 (0.64) RAB9ANPC1SMN1; SMN2USP2TP53
SCHEMBL256008 0.81 HSD11B1 (0.48) RAB9ANPC1SMN1; SMN2ALDH1A1MEN1
SCHEMBL28400273 0.80 HSD17B1 (0.43) RAB9ANPC1SMN1; SMN2ALDH1A1MEN1
SCHEMBL13458070 0.79 RAB9A (0.58) RAB9ANPC1SMN1; SMN2USP2TP53
SCHEMBL29664429 0.79 LMNA (0.43) RAB9ANPC1SMN1; SMN2TP53PKM
SCHEMBL1740270 0.79 LMNA (0.43) RAB9ANPC1SMN1; SMN2TP53PKM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107177589-A Modified active high-area carbon for fixing thimet degradation bacteria and preparation method thereof 光合强化(北京)生物科技有限公司 2017-09-19 CN claimed
US-8501731-B2 Derivatives of 6[3-(trifluoromethyl)phenyl]pyridazin-3(2H)-one having antitumor activity SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) 2013-08-06 US claimed
CN-1078350-A Synergistic composition and method for selective weed control CIBA GEIGY AG (CH) 1993-11-17 CN claimed
US-20250268910-A1 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS PHILIP MORRIS PRODUCTS S.A. (CH) 2025-08-28 US disclosed
EP-4559908-A1 HETEROARYL DERIVATIVE COMPOUND AND USE THEREOF S2CBio Inc. (KR) 2025-05-28 EP disclosed
US-12297209-B2 Benzodiazepine derivatives as RSV inhibitors ENANTA PHARMACEUTICALS, INC. (US) 2025-05-13 US disclosed
US-12268694-B2 Combination pharmaceutical agents as RSV inhibitors ENANTA PHARMACEUTICALS, INC. (US) 2025-04-08 US disclosed
CN-119095848-A Nicotinic acetylcholine receptor ligands 菲利普莫里斯生产公司 2024-12-06 CN disclosed
US-20240360155-A1 Benzodiazepine Derivatives as RSV Inhibitors ENANTA PHARM INC (US) 2024-10-31 US disclosed
US-20240336608-A1 IL4I1 INHIBITORS AND METHODS OF USE MERCK SHARP & DOHME LLC (US) 2024-10-10 US disclosed
CN-114478361-B Method for preparing aza-arene compound by coupling reaction without metal catalysis 浙江工业大学 2024-06-07 CN disclosed
US-4628088-A Preparation of substituted pyridazines ELI LILLY AND COMPANY (US) 1986-12-09 US disclosed
US-4623376-A PRE- AND POSTEMERGENCE AMERICAN CYANAMID COMPANY (US) 1986-11-18 US disclosed
US-4478999-A Process for the preparation of phenylpyridazine compounds CHEMIE LINZ AKTIENGESELLSCHAFT (AT) 1984-10-23 US disclosed
EP-0094038-A1 3-Amino-6-aryl-1,2,4-triazolo(4,3-b)pyridazines, their preparation and use HOECHST AKTIENGESELLSCHAFT (DE) 1983-11-16 EP disclosed
US-4293554-A Method of treating asthma AMERICAN CYANAMID COMPANY (US) 1981-10-06 US disclosed
US-4230705-A 6-Phenyl-1,2,4-triazolo[4,3-b]pyridazines and their uses in treating anxiety AMERICAN CYANAMID COMPANY (US) 1980-10-28 US disclosed
US-4111935-A BETA-ADRENERGIC BLOCKING AGENTS, VASODILATORS SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1978-09-05 US disclosed
US-4111935-A BETA-ADRENERGIC BLOCKING AGENTS, VASODILATORS SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1978-09-05 US disclosed
US-4092311-A Hypotensive alkyl-3-[6-(aryl)-3-pyridazinyl]-carbazates AMERICAN CYANAMID COMPANY (US) 1978-05-30 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 (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-20240360155-A1 Benzodiazepine Derivatives as RSV Inhibitors GABRA5, GABRA1, GABBR2 RAB9A 1384/4885NPC1 224/4885SMN1; SMN2 627/4885
US-12297209-B2 Benzodiazepine derivatives as RSV inhibitors GABRA5, GABRA1, GABBR2 RAB9A 1384/4885NPC1 224/4885SMN1; SMN2 627/4885
US-12268694-B2 Combination pharmaceutical agents as RSV inhibitors ACE, ACE2, SPCS3 RAB9A 384/4885NPC1 399/4885SMN1; SMN2 591/4885
US-20240336608-A1 IL4I1 INHIBITORS AND METHODS OF USE IL4I1, IL4, IL1RN RAB9A 1811/4885NPC1 706/4885SMN1; SMN2 2641/4885
US-20250268910-A1 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS CHRNA1, CHRNG, CHRM3 RAB9A 1403/4885NPC1 869/4885SMN1; SMN2 1610/4885

“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.