SCHEMBL762978

SCHEMBL762978

Cc1ccc(/C=N/O)cc1

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 3/20 0.64
RAB9A P51151 3/20 0.64
SMN1; SMN2 Q16637 2/20 0.64
CASP3 P42574 1/20 0.61
SENP8 Q96LD8 1/20 0.61
SENP7 Q9BQF6 1/20 0.61
SENP6 Q9GZR1 1/20 0.61
FGF23 Q9GZV9 4/20 0.57
GRIN2D O15399 2/20 0.54
GRIN3B O60391 2/20 0.54
GRIN1 Q05586 2/20 0.54
GRIN2A Q12879 2/20 0.54
GRIN2B Q13224 2/20 0.54
GRIN2C Q14957 2/20 0.54
GRIN3A Q8TCU5 2/20 0.54
KMT2A Q03164 3/20 0.52
ACHE P22303 1/20 0.52
GAA P10253 2/20 0.52
KDM4E B2RXH2 2/20 0.52
ALDH1A1 P00352 2/20 0.52

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
SCHEMBL2161965 1.00 NPC1 (0.64) NPC1RAB9ASMN1; SMN2CASP3SENP8
SCHEMBL2161969 1.00 NPC1 (0.64) NPC1RAB9ASMN1; SMN2CASP3SENP8
Hydrochloric Acid SCHEMBL28407082 0.97 NPC1 (0.61) NPC1RAB9ASMN1; SMN2CASP3SENP8
SCHEMBL10733330 0.87 NPC1 (0.65) NPC1RAB9ASMN1; SMN2CASP3SENP8
SCHEMBL5668373 0.86 KMT2A (0.64) NPC1RAB9ASMN1; SMN2CASP3SENP8
SCHEMBL4275687 0.86 KMT2A (0.64) NPC1RAB9ASMN1; SMN2CASP3SENP8
SCHEMBL4275683 0.86 KMT2A (0.64) NPC1RAB9ASMN1; SMN2CASP3SENP8
SCHEMBL2608307 0.78 NPC1 (1.00) NPC1RAB9ASMN1; SMN2CASP3SENP8
SCHEMBL11743247 0.78 NPC1 (1.00) NPC1RAB9ASMN1; SMN2CASP3SENP8
SCHEMBL9377205 0.76 SMN1; SMN2 (0.67) NPC1RAB9ASMN1; SMN2GRIN2DGRIN3B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118718469-A Safe and efficient extracting agent for removing phenol and oil and application thereof 中国科学院过程工程研究所 2024-10-01 CN claimed
CN-118184675-A Mugwort lactone I derivative and pharmaceutical composition thereof, and preparation method and application thereof 中国科学院昆明植物研究所 2024-06-14 CN claimed
CN-114835660-B Preparation method of oxime ether 浙江理工大学 2024-03-22 CN claimed
CN-114835660-A Preparation method of oxime ether 浙江理工大学 2022-08-02 CN claimed
EP-1527165-A4 A RHODOCOCCUS GENE ENCODING ALDOXIME DEHYDRATASE DU PONT (US) 2006-06-07 EP claimed
EP-1527165-A2 A RHODOCOCCUS GENE ENCODING ALDOXIME DEHYDRATASE E.I. du Pont de Nemours and Company (US) 2005-05-04 EP claimed
US-20030215929-A1 Rhodococcus gene encoding aldoxime dehydratase E. I. DU PONT DE NEMOURS AND COMPANY 2003-11-20 US claimed
WO-2003078581-A2 A RHODOCOCCUS GENE ENCODING ALDOXIME DEHYDRATASE E.I. DU PONT DE NEMOURS AND COMPANY (US) 2003-09-25 WO claimed
CN-119930463-A Asymmetric catalytic synthesis method of oxime ether compound with high optical purity 南方科技大学 2025-05-06 CN disclosed
US-20250109095-A1 METHOD FOR PREPARING OXIME DERIVATIVE SEOUL NATIONAL UNIVERSITY R&DB FOUNDATION (KR) 2025-04-03 US disclosed
EP-4522608-A1 PYRROLIDINONE DERIVATIVES AS INHIBITORS OF NF KAPPA B INDUCING KINASE JANSSEN Pharmaceutica NV (BE) 2025-03-19 EP disclosed
CN-118718469-A Safe and efficient extracting agent for removing phenol and oil and application thereof 中国科学院过程工程研究所 2024-10-01 CN disclosed
CN-114450271-B Ureas, amino and substituted heteroaryl compounds for Cbl-b inhibition 纽力克斯治疗公司 2024-09-20 CN disclosed
CN-118184675-A Mugwort lactone I derivative and pharmaceutical composition thereof, and preparation method and application thereof 中国科学院昆明植物研究所 2024-06-14 CN disclosed
WO-2003078581-A2 A RHODOCOCCUS GENE ENCODING ALDOXIME DEHYDRATASE E.I. DU PONT DE NEMOURS AND COMPANY (US) 2003-09-25 WO disclosed
US-20030171618-A1 Process for producing organic compounds using nitrites DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2003-09-11 US disclosed
EP-1342715-A2 Process for producing oximes using nitirites Daicel Chemical Industries, Ltd. (JP) 2003-09-10 EP disclosed
US-5284853-A Hypotensive agents AMERICAN CYANAMID COMPANY (US) 1994-02-08 US disclosed
US-5281604-A Pharmaceuticals AMERICAN CYANAMID COMPANY (US) 1994-01-25 US disclosed
US-4581365-A Trichloroacryloyl oxime fungicides NIHON TOKUSHU NOYAKU SEIZO K.K. (JP) 1986-04-08 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-20030171618-A1 Process for producing organic compounds using nitrites NOS1, NOS2, NOS3 NPC1 2514/4885RAB9A 3256/4885SMN1; SMN2 1519/4885
US-20250109095-A1 METHOD FOR PREPARING OXIME DERIVATIVE NOS2, NOS1, NOS3 NPC1 4600/4885RAB9A 4013/4885SMN1; SMN2 758/4885

“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.