SCHEMBL744645

SCHEMBL744645

O=C(O)c1cc(Cl)cc2cccnc12

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.53
LMNA P02545 2/20 0.51
SMN1; SMN2 Q16637 2/20 0.51
STING1 Q86WV6 1/20 0.51
MAPT P10636 2/20 0.50
PLEC Q15149 1/20 0.50
SLC40A1 Q9NP59 1/20 0.49
ALOX12 P18054 1/20 0.49
L3MBTL1 Q9Y468 3/20 0.49
CCR1 P32246 1/20 0.49
CCR8 P51685 1/20 0.49
PARP1 P09874 1/20 0.47
PDE4A P27815 1/20 0.46
PDE4C Q08493 1/20 0.46
PDE4D Q08499 1/20 0.46
KDR P35968 1/20 0.46
KDM4E B2RXH2 4/20 0.46
DHODH Q02127 2/20 0.46
TDP1 Q9NUW8 1/20 0.46
KDM6B O15054 1/20 0.45

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
SCHEMBL24338474 0.81 KDM4E (0.50) ALDH1A1SLC40A1L3MBTL1CCR1CCR8
SCHEMBL11429773 0.81 ALDH1A1 (0.58) ALDH1A1LMNASMN1; SMN2MAPTPLEC
SCHEMBL29089214 0.81 ALDH1A1 (0.54) ALDH1A1LMNASMN1; SMN2MAPTPLEC
SCHEMBL30605381 0.81 ALDH1A1 (0.54) ALDH1A1LMNASMN1; SMN2MAPTPLEC
SCHEMBL68215 0.81 ALDH1A1 (0.54) ALDH1A1LMNASMN1; SMN2MAPTPLEC
SCHEMBL8544466 0.80 ALDH1A1 (0.53) ALDH1A1LMNASMN1; SMN2MAPTPLEC
SCHEMBL21816294 0.80 PSMD14 (0.56) ALDH1A1LMNAMAPTPLECSLC40A1
SCHEMBL4602037 0.80 ALDH1A1 (0.53) ALDH1A1LMNASMN1; SMN2MAPTPLEC
SCHEMBL679992 0.78 KDM4E (0.60) ALDH1A1LMNAMAPTALOX12L3MBTL1
SCHEMBL14820315 0.78 MEN1 (0.53) ALDH1A1LMNASMN1; SMN2MAPTPLEC

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12024509-B2 Therapeutic compounds as inhibitors of the orexin-1 receptor C4X DISCOVERY LIMITED (GB) 2024-07-02 US disclosed
CN-115515956-A Benzimidazole derivative and preparation method and medical application thereof 深圳信立泰药业股份有限公司 2022-12-23 CN disclosed
WO-2022068772-A1 BENZIMIDAZOLE DERIVATIVE, AND PREPARATION METHOD THEREFOR, AND MEDICAL USE THEREOF 深圳信立泰药业股份有限公司 2022-04-07 WO disclosed
CN-107074808-B Therapeutic compounds as orexin-1 receptor inhibitors 希四克斯探索有限公司 2021-03-02 CN disclosed
EP-3189043-B1 THERAPEUTIC COMPOUNDS AS INHIBITORS OF THE OREXIN-1 RECEPTOR C4X DISCOVERY LTD (GB) 2020-11-18 EP disclosed
US-20200270247-A1 THERAPEUTIC COMPOUNDS AS INHIBITORS OF THE OREXIN-1 RECEPTOR C4X DISCOVERY LIMITED 2020-08-27 US disclosed
US-10611760-B2 Therapeutic compounds as inhibitors of the orexin-1 receptor C4X DISCOVERY LIMITED (GB) 2020-04-07 US disclosed
US-20170291897-A1 THERAPEUTIC COMPOUNDS AS INHIBITORS OF THE OREXIN-1 RECEPTOR INDIVIOR INC. 2017-10-12 US disclosed
CN-107074808-A It is used as the therapeutic compound of the acceptor inhibitor of orexin 1 希四克斯探索有限公司 2017-08-18 CN disclosed
EP-3189043-A1 THERAPEUTIC COMPOUNDS AS INHIBITORS OF THE OREXIN-1 RECEPTOR C4x Discovery Limited (GB) 2017-07-12 EP disclosed
US-20080153883-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS AND USES THEREOF ABBOTT LABORATORIES (US) 2008-06-26 US disclosed
WO-2008059513-A2 COMPOUNDS SUITABLE AS MODULATORS OF HDL CADILA HEALTHCARE LIMITED (IN) 2008-05-22 WO disclosed
US-20080058335-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS AND USES THEREOF ABBVIE INC. 2008-03-06 US disclosed
WO-2007140385-A2 THIAZOLE COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS AND USES THEREOF ABBOTT LABORATORIES (US) 2007-12-06 WO disclosed
EP-0085182-B1 PROCESS FOR THE PREPARATION OF QUINOLINE MONOCARBOXYLIC ACID BASF Aktiengesellschaft (DE) 1986-04-23 EP disclosed
EP-0085182-A2 Process for the preparation of quinoline monocarboxylic acid BASF Aktiengesellschaft (DE) 1983-08-10 EP disclosed
US-4278680-A Hypoglycaemically and hypolipidaemically active derivatives of phenylacetic acid BOEHRINGER MANNHEIM GMBH (DE) 1981-07-14 US disclosed
US-4221815-A HYPOGLYCEMIC AGENTS HOECHST AKTIENGESELLSCHAFT (DE) 1980-09-09 US disclosed
US-4207341-A Hypoglycaemically and hypolipidaemically active derivatives of phenylacetic acid BOEHRINGER-MANNHEIM GMBH (DE) 1980-06-10 US disclosed
US-4158063-A Acylamino(alkyl)benzene derivatives and process for preparing them HOECHST AKTIENGESELLSCHAFT (DE) 1979-06-12 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 (6 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-12024509-B2 Therapeutic compounds as inhibitors of the orexin-1 receptor HCRTR1, HCRTR2, NPY1R ALDH1A1 1458/4885LMNA 3283/4885SMN1; SMN2 2154/4885
US-20200270247-A1 THERAPEUTIC COMPOUNDS AS INHIBITORS OF THE OREXIN-1 RECEPTOR HCRTR1, HCRTR2, NPY1R ALDH1A1 1458/4885LMNA 3283/4885SMN1; SMN2 2154/4885
US-10611760-B2 Therapeutic compounds as inhibitors of the orexin-1 receptor HCRTR1, HCRTR2, NPY1R ALDH1A1 1458/4885LMNA 3283/4885SMN1; SMN2 2154/4885
US-20170291897-A1 THERAPEUTIC COMPOUNDS AS INHIBITORS OF THE OREXIN-1 RECEPTOR HCRTR1, HCRTR2, NPY1R ALDH1A1 1458/4885LMNA 3283/4885SMN1; SMN2 2154/4885
US-20080058335-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS AND USES THEREOF CNR1, CNR2, OPRL1 ALDH1A1 914/4885LMNA 1150/4885SMN1; SMN2 2336/4885
US-20080153883-A1 NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS AND USES THEREOF CNR1, CNR2, GPR18 ALDH1A1 1654/4885LMNA 3880/4885SMN1; SMN2 3736/4885

“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.