SCHEMBL21360469

SCHEMBL21360469

O=Cc1c(-c2ccc(F)cc2)nc2ccccn12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 1.00
NPC1 O15118 5/20 0.74
RAB9A P51151 5/20 0.74
KDM4E B2RXH2 6/20 0.69
SMN1; SMN2 Q16637 2/20 0.69
HPGD P15428 1/20 0.55
TUBB4A P04350 1/20 0.53
TUBB P07437 1/20 0.53
TUBA3C P0DPH7 1/20 0.53
TUBA1B P68363 1/20 0.53
TUBA4A P68366 1/20 0.53
TUBB4B P68371 1/20 0.53
TUBB3 Q13509 1/20 0.53
TUBB2A Q13885 1/20 0.53
TUBB8 Q3ZCM7 1/20 0.53
TUBA3E Q6PEY2 1/20 0.53
TUBA1A Q71U36 1/20 0.53
TUBA1C Q9BQE3 1/20 0.53
TUBB6 Q9BUF5 1/20 0.53
TUBB2B Q9BVA1 1/20 0.53

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
SCHEMBL4773388 0.88 ALDH1A1 (0.78) ALDH1A1NPC1RAB9AKDM4ESMN1; SMN2
SCHEMBL1430465 0.85 NPC1 (0.74) ALDH1A1NPC1RAB9AKDM4ESMN1; SMN2
SCHEMBL22001460 0.85 NPC1 (0.74) ALDH1A1NPC1RAB9AKDM4ESMN1; SMN2
SCHEMBL9587009 0.85 NPC1 (1.00) ALDH1A1NPC1RAB9AKDM4ESMN1; SMN2
SCHEMBL1430562 0.82 ALDH1A1 (0.69) ALDH1A1NPC1RAB9AKDM4ESMN1; SMN2
SCHEMBL18952383 0.82 ALDH1A1 (0.69) ALDH1A1NPC1RAB9AKDM4ESMN1; SMN2
SCHEMBL18952249 0.82 NPC1 (0.73) ALDH1A1NPC1RAB9AKDM4ESMN1; SMN2
SCHEMBL18952253 0.82 ALDH1A1 (0.73) ALDH1A1NPC1RAB9AKDM4ESMN1; SMN2
SCHEMBL29614093 0.81 RAB9A (0.68) ALDH1A1NPC1RAB9AKDM4ESMN1; SMN2
SCHEMBL1429286 0.81 ALDH1A1 (0.67) ALDH1A1NPC1RAB9AKDM4ESMN1; SMN2

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025082731-A1 INTRANASAL FORMULATIONS FOR TREATING OBSTRUCTIVE SLEEP APNEA MOSANNA THERAPEUTICS AG (CH) 2025-04-24 WO disclosed
US-10759794-B2 2-phenyl-3-(piperazinomethyl)imidazo[1,2-A]pyridine derivatives as blockers of task-1 and task-2 channels, for the treatment of sleep-related breathing disorders BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2020-09-01 US disclosed
EP-3386979-B1 2-PHENYL-3-(PIPERAZINOMETHYL)IMIDAZO[1,2-A]PYRIDINE DERIVATIVES AS BLOCKERS OF THE TASK-1 AND TASK-2 CHANNELS FOR TREATING SLEEP-RELATED BREATHING DISORDERS Bayer Pharma AG (DE) 2020-07-29 EP disclosed
EP-3386979-B1 2-PHENYL-3-(PIPERAZINOMETHYL)IMIDAZO[1,2-A]PYRIDINE DERIVATIVES AS BLOCKERS OF THE TASK-1 AND TASK-2 CHANNELS FOR TREATING SLEEP-RELATED BREATHING DISORDERS Bayer Pharma AG (DE) 2020-07-29 EP disclosed
US-10414765-B2 Substituted perhydropyrrolo[3,4-c]pyrrole derivatives and the use of same BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2019-09-17 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 (2 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-10414765-B2 Substituted perhydropyrrolo[3,4-c]pyrrole derivatives and the use of same PAH, EGLN3, HYOU1 ALDH1A1 796/4885NPC1 388/4885RAB9A 4337/4885
US-10759794-B2 2-phenyl-3-(piperazinomethyl)imidazo[1,2-A]pyridine derivatives as blockers of task-1 and task-2 channels, for the treatment of sleep-related breathing disorders TRPV2, CACNA1G, KCNJ2 ALDH1A1 2314/4885NPC1 813/4885RAB9A 4129/4885

“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.