SCHEMBL2440282

SCHEMBL2440282

O=C(OCc1ccccc1)N1CCCC(O)C1

nearest known ligand 0.60

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.60
NPC1 O15118 2/20 0.60
RAB9A P51151 2/20 0.60
CYP2C19 P33261 1/20 0.58
KMT2A Q03164 2/20 0.55
MEN1 O00255 1/20 0.55
NPSR1 Q6W5P4 1/20 0.55
ALDH1A1 P00352 2/20 0.53
PRMT5 O14744 1/20 0.52
WDR77 Q9BQA1 1/20 0.52
JAK2 O60674 2/20 0.51
JAK1 P23458 2/20 0.51
TYK2 P29597 2/20 0.51
JAK3 P52333 2/20 0.51
PREP P48147 1/20 0.50
PDE4B Q07343 1/20 0.49
GRIN2B Q13224 1/20 0.49
HTT P42858 1/20 0.49
USP30 Q70CQ3 1/20 0.48

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
SCHEMBL6128832 1.00 SMN1; SMN2 (0.60) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A
SCHEMBL5368396 1.00 SMN1; SMN2 (0.60) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A
SCHEMBL16903351 0.96 SMN1; SMN2 (0.59) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A
Formic Acid SCHEMBL28339396 0.95 SMN1; SMN2 (0.55) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A
SCHEMBL18084804 0.95 SMN1; SMN2 (0.58) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A
SCHEMBL1841984 0.92 SMN1; SMN2 (0.68) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A
SCHEMBL492951 0.92 SMN1; SMN2 (0.68) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A
SCHEMBL18084813 0.92 SMN1; SMN2 (0.68) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A
SCHEMBL540519 0.92 SMN1; SMN2 (0.68) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A
SCHEMBL13547248 0.89 SMN1; SMN2 (0.68) SMN1; SMN2NPC1RAB9ACYP2C19KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118791425-A Synthesis method of 1-BOC-3-piperidone and similar cyclic ketone compounds thereof 浙江尚科生物医药有限公司 2024-10-18 CN claimed
US-20250388606-A1 AZAQUINAZOLINE PAN-KRAS INHIBITORS MIRATI THERAPEUTICS INC (US) 2025-12-25 US disclosed
EP-4626865-A1 CYCLIC PYRAZOLE DIAMIDE IRE1/XBP1S ACTIVATORS Protego Biopharma, Inc. (US) 2025-10-08 EP disclosed
US-12398154-B2 Azaquinazoline pan-KRas inhibitors Mirati Therapeutics, Inc. (US) 2025-08-26 US disclosed
EP-4587446-A1 BIFUNCTIONAL COMPOUNDS AND PHARMACEUTICAL USES THEREOF Risen (Suzhou) Pharma Tech Co., Ltd. (CN) 2025-07-23 EP disclosed
US-20250136606-A1 MODULATORS OF TRPML, THEIR COMPOSITIONS AND METHODS OF USE CARAWAY THERAPEUTICS, INC. (US) 2025-05-01 US disclosed
US-20240368150-A1 BICYCLIC TETRAHYDROAZEPINE DERIVATIVES FOR THE TREATMENT OF CANCER HOFFMANN-LA ROCHE INC. (US) 2024-11-07 US disclosed
CN-118791425-A Synthesis method of 1-BOC-3-piperidone and similar cyclic ketone compounds thereof 浙江尚科生物医药有限公司 2024-10-18 CN disclosed
EP-4408850-A1 MODULATORS OF TRPML, THEIR COMPOSITIONS AND METHODS OF USE Caraway Therapeutics, Inc. (US) 2024-08-07 EP disclosed
CN-115003671-B JNK inhibitors, pharmaceutical compositions and uses thereof 武汉朗来科技发展有限公司 2024-08-06 CN disclosed
EP-0723545-A1 QUINOLIZINONE TYPE COMPOUNDS ABBOTT LABORATORIES (US) 1996-07-31 EP disclosed
EP-0487411-B1 Erythromycin derivatives, their preparation, intermediates obtained and their application as medicaments ROUSSEL UCLAF (FR) 1996-01-31 EP disclosed
EP-0690847-A1 HETEROCYCLIC COMPOUNDS AS PLATELET AGGREGATION INHIBITORS ZENECA LIMITED (GB) 1996-01-10 EP disclosed
US-5444051-A BACTERICIDES ROUSSEL UCLAF (FR) 1995-08-22 US disclosed
WO-1995010519-A1 QUINOLIZINONE TYPE COMPOUNDS ABBOTT LABORATORIES (US) 1995-04-20 WO disclosed
US-5407943-A Azaspiro quinolone antibacterial agents PFIZER INC. (US) 1995-04-18 US disclosed
EP-0641339-A1 AZASPIRO QUINOLONE ANTIBACTERIAL AGENTS PFIZER INC. (US) 1995-03-08 EP disclosed
WO-1994022835-A2 HETEROCYCLIC COMPOUNDS AS PLATELET AGGREGATION INHIBITORS ZENECA LIMITED (GB) 1994-10-13 WO disclosed
WO-1992022550-A1 AZASPIRO QUINOLONE ANTIBACTERIAL AGENTS PFIZER INC. (US) 1992-12-23 WO disclosed
EP-0487411-A1 Erythromycin derivatives, their preparation, intermediates obtained and their application as medicaments ROUSSEL UCLAF (FR) 1992-05-27 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 (4 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-20240368150-A1 BICYCLIC TETRAHYDROAZEPINE DERIVATIVES FOR THE TREATMENT OF CANCER BICRA, BRD4, CNR1 SMN1; SMN2 3375/4885NPC1 1363/4885RAB9A 1690/4885
US-20250136606-A1 MODULATORS OF TRPML, THEIR COMPOSITIONS AND METHODS OF USE MCOLN1, TRPM2, PKD2 SMN1; SMN2 1638/4885NPC1 43/4885RAB9A 1163/4885
US-12398154-B2 Azaquinazoline pan-KRas inhibitors KRAS, NRAS, HRAS SMN1; SMN2 4444/4885NPC1 2647/4885RAB9A 55/4885
US-20250388606-A1 AZAQUINAZOLINE PAN-KRAS INHIBITORS KRAS, NRAS, HRAS SMN1; SMN2 4096/4885NPC1 1305/4885RAB9A 45/4885

“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.