SCHEMBL2234353

SCHEMBL2234353

Cc1nc(N)nc(C)c1Br

nearest known ligand 0.55

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.55
TLR8 Q9NR97 2/20 0.48
ALDH1A1 P00352 4/20 0.46
KDM4E B2RXH2 2/20 0.46
NR1I2 O75469 1/20 0.46
AHR P35869 1/20 0.46
GAA P10253 1/20 0.43
IKBKB O14920 2/20 0.41
IKBKE Q14164 1/20 0.41
CYP1A2 P05177 1/20 0.39
HPGD P15428 1/20 0.39
NUDT1 P36639 1/20 0.39
HSD17B10 Q99714 1/20 0.39
IDO1 P14902 1/20 0.39
MAP3K14 Q99558 1/20 0.37
HSP90AB1 P08238 1/20 0.33
TLR7 Q9NYK1 1/20 0.33
RAB9A P51151 1/20 0.32
TDP1 Q9NUW8 1/20 0.32

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
SCHEMBL13851094 0.88 LMNA (0.56) LMNATLR8ALDH1A1KDM4ENR1I2
Bromide SCHEMBL8547428 0.86 LMNA (0.61) LMNATLR8ALDH1A1KDM4ENR1I2
SCHEMBL10161427 0.84 LMNA (0.46) LMNATLR8ALDH1A1KDM4ENR1I2
SCHEMBL1983684 0.82 NR1I2 (0.47) LMNATLR8ALDH1A1KDM4ENR1I2
SCHEMBL2396549 0.82 LMNA (0.44) LMNATLR8ALDH1A1KDM4ENR1I2
SCHEMBL26978230 0.78 ALDH1A1 (0.51) LMNATLR8ALDH1A1KDM4ENR1I2
SCHEMBL15688197 0.77 LMNA (0.40) LMNATLR8ALDH1A1KDM4ENR1I2
SCHEMBL19174177 0.75 LMNA (0.39) LMNATLR8ALDH1A1KDM4ENR1I2
SCHEMBL21963176 0.75 LMNA (0.55) LMNATLR8ALDH1A1KDM4ENR1I2
SCHEMBL9644113 0.73 ALDH1A1 (0.50) LMNATLR8ALDH1A1KDM4ECYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110028457-B Isotope labeled sulfabromodimethyl pyrimidine and synthesis method thereof 深圳出入境检验检疫局食品检验检疫技术中心 2023-01-20 CN claimed
CN-110028457-A A kind of sulfabromomethazine and its synthetic method of stable isotope labeling 深圳出入境检验检疫局食品检验检疫技术中心 2019-07-19 CN claimed
EP-4744661-A2 NOVEL PYRIMIDIN-2-YL SULFONAMIDE DERIVATIVES F. Hoffmann-La Roche AG (CH) 2026-05-20 EP disclosed
EP-4676923-A1 BIARYLAMIDE DERIVATIVES AND THEIR USE AS PKMYT1 INHIBITORS Cancer Research Technology Limited (GB) 2026-01-14 EP disclosed
EP-4298092-B1 NOVEL PYRIMIDIN-2-YL SULFONAMIDE DERIVATIVES HOFFMANN LA ROCHE (CH) 2025-11-26 EP disclosed
US-20250304600-A1 PHARMACEUTICAL COMPOUNDS AND COMPOSITIONS AS c-KIT KINASE INHIBITORS ENANTA PHARMACEUTICALS, INC. 2025-10-02 US disclosed
EP-4608988-A1 CLOSED-LOOP OPTIMIZATION OF GENERAL REACTION CONDITIONS FOR HETEROARYL SUZUKI-MIYAURA COUPLING THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2025-09-03 EP disclosed
EP-4267574-B1 6-HETEROARYLOXY BENZIMIDAZOLES AND AZABENZIMIDAZOLES AS JAK2 INHIBITORS AJAX THERAPEUTICS INC (US) 2025-04-23 EP disclosed
US-20250059174-A1 Pharmaceutical Compounds and Compositions as C-Kit Kinase Inhibitors ENANTA PHARM INC (US) 2025-02-20 US disclosed
WO-2025034951-A1 PHARMACEUTICAL COMPOUNDS AND COMPOSITIONS AS C-KIT KINASE INHIBITORS ENANTA PHARMACEUTICALS, INC. (US) 2025-02-13 WO disclosed
US-20240327390-A1 SUBSTITUTED NITROGEN CONTAINING COMPOUNDS BRISTOL MYERS SQUIBB CO (US) 2024-10-03 US disclosed
US-6506761-B1 Compound of the invention are active as inhibitors of Thrombin and are useful in treating disease states in mammals which are characterized by abnormal thrombosis and have the following structure: CORVAS INTERNATIONAL, INC. 2003-01-14 US disclosed
US-6506754-B1 Compounds as anticoagulants CORVAS INTERNATIONAL, INC. 2003-01-14 US disclosed
US-6506760-B1 Compounds of the invention are active as inhibitors of Thrombin and are useful in treating disease states in mammals which are characterized by abnormal thrombosis and have the following structure: CORVAS INTERNATIONAL, INC. 2003-01-14 US disclosed
EP-0174272-B1 PROCESS FOR THE PREPARATION OF DIMETHYLMALEIC ANHYDRIDE CIBA-GEIGY AG (CH) 1988-08-31 EP disclosed
EP-0175641-B1 PROCESS FOR THE PREPARATION OF DIMETHYLMALEIC ANHYDRIDE CIBA-GEIGY AG (CH) 1988-02-24 EP disclosed
US-4644069-A HEATING MALEIC ACID OR ANHYDRIDE WITH AN AMIDINE OR ITS SALT CIBA-GEIGY CORPORATION (US) 1987-02-17 US disclosed
US-4639531-A HETEROCYCLIC AMIDINE CATALYST CIBA-GEIGY CORPORATION (US) 1987-01-27 US disclosed
EP-0175641-A1 Process for the preparation of dimethylmaleic anhydride CIBA-GEIGY AG (CH) 1986-03-26 EP disclosed
EP-0174272-A1 Process for the preparation of dimethylmaleic anhydride CIBA-GEIGY AG (CH) 1986-03-12 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 (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-20240327390-A1 SUBSTITUTED NITROGEN CONTAINING COMPOUNDS NR0B1, GRK1, GRIN1 LMNA 610/4885TLR8 1672/4885ALDH1A1 2289/4885
US-20250304600-A1 PHARMACEUTICAL COMPOUNDS AND COMPOSITIONS AS c-KIT KINASE INHIBITORS KIT, PDGFRA, PDGFRB LMNA 1994/4885TLR8 2986/4885ALDH1A1 1140/4885
US-20250059174-A1 Pharmaceutical Compounds and Compositions as C-Kit Kinase Inhibitors KIT, PDGFRA, PDGFRB LMNA 1994/4885TLR8 2986/4885ALDH1A1 1140/4885

“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.