SCHEMBL4201340

SCHEMBL4201340

Clc1nc(-c2ccc(-c3ccccc3)cc2)nc(-c2ccc(-c3ccccc3)cc2)n1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 4/20 0.54
MEN1 O00255 7/20 0.54
KMT2A Q03164 7/20 0.54
HTT P42858 1/20 0.54
ALDH1A1 P00352 6/20 0.52
HPGD P15428 5/20 0.52
SMN1; SMN2 Q16637 3/20 0.52
LMNA P02545 5/20 0.50
KDM4E B2RXH2 4/20 0.50
MAPT P10636 3/20 0.50
GLA P06280 2/20 0.50
CYP1A2 P05177 1/20 0.50
POLB P06746 1/20 0.48
ADORA3 P0DMS8 1/20 0.48
ADORA2A P29274 1/20 0.48
ADORA2B P29275 1/20 0.48
ADORA1 P30542 1/20 0.48
TDP1 Q9NUW8 2/20 0.47
NPC1 O15118 2/20 0.46
RAB9A P51151 2/20 0.46

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
SCHEMBL16332656 1.00 L3MBTL1 (0.54) L3MBTL1MEN1KMT2AHTTALDH1A1
SCHEMBL18468590 1.00 L3MBTL1 (0.54) L3MBTL1MEN1KMT2AHTTALDH1A1
SCHEMBL18468613 1.00 L3MBTL1 (0.54) L3MBTL1MEN1KMT2AHTTALDH1A1
SCHEMBL29385431 1.00 L3MBTL1 (0.54) L3MBTL1MEN1KMT2AHTTALDH1A1
SCHEMBL4031522 0.95 MEN1 (0.54) L3MBTL1MEN1KMT2AHTTALDH1A1
SCHEMBL106948 0.95 L3MBTL1 (0.58) L3MBTL1MEN1KMT2AHTTALDH1A1
SCHEMBL28243450 0.95 L3MBTL1 (0.58) L3MBTL1MEN1KMT2AHTTALDH1A1
SCHEMBL18469030 0.94 MEN1 (0.52) L3MBTL1MEN1KMT2AHTTALDH1A1
SCHEMBL24523212 0.92 MEN1 (0.50) L3MBTL1MEN1KMT2AHTTALDH1A1
SCHEMBL20560781 0.92 MEN1 (0.50) L3MBTL1MEN1KMT2AHTTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112321585-B Asymmetric substituted diphenyl pyridine compound and preparation and application thereof 华南理工大学 2022-04-22 CN claimed
US-12635409-B2 Organic electroluminescent materials and devices UNIVERSAL DISPLAY CORPORATION (US) 2026-05-19 US disclosed
US-20260123278-A1 COMPOUND FOR ORGANIC ELECTRONIC DEVICE, ORGANIC ELECTRONIC DEVICE USING THE SAME, AND ELECTRONIC DEVICE THEREOF DUK SAN NEOLUX CO., LTD. (KR) 2026-04-30 US disclosed
US-12577215-B2 Triazine UV absorbers and a process for the preparation thereof BASF SE (DE) 2026-03-17 US disclosed
EP-4167707-B1 ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES UNIVERSAL DISPLAY CORP (US) 2025-12-10 EP disclosed
EP-4658226-A1 COMPOSITION COMPRISING 1,3,5-TRIAZINE, 2,4,6-TRIS[1,1'-BIPHENYL]-4-YL WITH LOWER AMOUNTS OF IMPURITIES BASF SE (DE) 2025-12-10 EP disclosed
EP-4658234-A1 COMPOSITION COMPRISING 1,3,5-TRIAZINE, 2,4,6-TRIS[1,1'-BIPHENYL]-4-YL WITH LOWER AMOUNTS OF IMPURITIES BASF SE (DE) 2025-12-10 EP disclosed
US-12490652-B2 Organic optoelectronic device and display device SAMSUNG SDI CO., LTD. (KR) 2025-12-02 US disclosed
EP-3981762-B1 NITROGEN-CONTAINING COMPOUND, ELECTRONIC ELEMENT, AND ELECTRONIC DEVICE SHAANXI LIGHTE OPTOELECTRONICS MAT CO LTD (CN) 2025-10-15 EP disclosed
US-12428409-B2 Compound, material for organic electroluminescent elements, organic electroluminescent element, and electronic device IDEMITSU KOSAN CO., LTD. (JP) 2025-09-30 US disclosed
US-20050165231-A1 Process for making triazine UV absorbers using Lewis acids and reaction promoters GUPTA RAM B (US) 2005-07-28 US disclosed
US-6900314-B2 Process for making triazine UV absorbers using lewis acids and reaction promoters CYTEC TECHNOLOGY CORP. (US) 2005-05-31 US disclosed
US-20040204585-A1 Process for making triazine UV absorbers using lewis acids and reaction promoters GUPTA RAM B (US) 2004-10-14 US disclosed
US-6730785-B2 COMPRISING LEWIS ACID AND REACTION PROMOTER IN AN AMOUNT SUFFICIENT TO SYNTHESIZE TRIAZINE COMPOUNDS AT LOWER REACTION TEMPERATURES, GREATER YIELDS, OR HIGHER SELECTIVITIES COMPARED TO LEWIS ACID ALONE CYTEC TECHNOLOGY CORP. 2004-05-04 US disclosed
US-6710177-B2 REACTING A CYANURIC HALIDE WITH BENZENE COMPOUND CYTEC TECHNOLOGY CORP. 2004-03-23 US disclosed
US-6486316-B1 Process for making triazine UV absorbers using Lewis acids and reaction promoters CYTEC TECHNOLOGY CORP. 2002-11-26 US disclosed
US-20020013463-A1 Process for making triazine UV absorbers using Lewis acids and reaction promoters CYTEC INDUSTRIES CORP. 2002-01-31 US disclosed
EP-1131305-A1 PROCESS FOR PREPARING TRIAZINES USING A COMBINATION OF LEWIS ACIDS WITH REACTION PROMOTERS CYTEC TECHNOLOGY CORP. (US) 2001-09-12 EP disclosed
US-20010020094-A1 Process for making triazine UV absorbers using lewis acids and reaction promoters CYTEC TECHNOLOGIES CORP. 2001-09-06 US disclosed
WO-2000029392-A1 PROCESS FOR PREPARING TRIAZINES USING A COMBINATION OF LEWIS ACIDS AND REACTION PROMOTERS CYTEC TECHNOLOGY CORP. (US) 2000-05-25 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 (8 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-20260123278-A1 COMPOUND FOR ORGANIC ELECTRONIC DEVICE, ORGANIC ELECTRONIC DEVICE USING THE SAME, AND ELECTRONIC DEVICE THEREOF SCO2, AOC2, PIEZO1 L3MBTL1 749/4885MEN1 3332/4885KMT2A 1740/4885
US-12635409-B2 Organic electroluminescent materials and devices NSUN2, CTNND1, NSD1 L3MBTL1 2025/4885MEN1 2106/4885KMT2A 949/4885
US-20040204585-A1 Process for making triazine UV absorbers using lewis acids and reaction promoters TYR, TDO2, CYP4Z1 L3MBTL1 948/4885MEN1 4176/4885KMT2A 461/4885
US-12428409-B2 Compound, material for organic electroluminescent elements, organic electroluminescent element, and electronic device L1CAM, MLX, LEF1 L3MBTL1 136/4885MEN1 204/4885KMT2A 1587/4885
US-20020013463-A1 Process for making triazine UV absorbers using Lewis acids and reaction promoters TYR, TDO2, CYP4Z1 L3MBTL1 948/4885MEN1 4176/4885KMT2A 461/4885
US-20050165231-A1 Process for making triazine UV absorbers using Lewis acids and reaction promoters TYR, TDO2, CYP4Z1 L3MBTL1 948/4885MEN1 4176/4885KMT2A 461/4885
US-12577215-B2 Triazine UV absorbers and a process for the preparation thereof CYP2R1, NR2E3, SRD5A2 L3MBTL1 4326/4885MEN1 2125/4885KMT2A 3508/4885
US-20010020094-A1 Process for making triazine UV absorbers using lewis acids and reaction promoters TYR, TDO2, CYP4Z1 L3MBTL1 948/4885MEN1 4176/4885KMT2A 461/4885

“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.