SCHEMBL4864755

SCHEMBL4864755

COc1ccc(C(C)=NO)cc1OC

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.64
SMN1; SMN2 Q16637 3/20 0.64
POLB P06746 1/20 0.64
GAA P10253 4/20 0.61
MEN1 O00255 1/20 0.61
KMT2A Q03164 1/20 0.61
CYP2C9 P11712 2/20 0.57
CYP2C19 P33261 2/20 0.57
TSHR P16473 2/20 0.57
CYP1A2 P05177 1/20 0.57
CYP3A4 P08684 1/20 0.57
CA12 O43570 1/20 0.55
CA1 P00915 1/20 0.55
CA2 P00918 1/20 0.55
CA4 P22748 1/20 0.55
CA6 P23280 1/20 0.55
CA7 P43166 1/20 0.55
TPMT P51580 1/20 0.55
CA9 Q16790 1/20 0.55
CA14 Q9ULX7 1/20 0.55

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
SCHEMBL29467205 1.00 MAPT (0.64) MAPTSMN1; SMN2POLBGAAMEN1
SCHEMBL12585063 0.85 ALOX15 (0.50) MAPTSMN1; SMN2POLBGAAMEN1
SCHEMBL13268873 0.85 GAA (0.63) MAPTPOLBGAAMEN1KMT2A
SCHEMBL17548941 0.85 GAA (0.63) MAPTPOLBGAAMEN1KMT2A
SCHEMBL14632560 0.83 MAPT (0.46) MAPTSMN1; SMN2POLBGAAMEN1
SCHEMBL14632561 0.83 MAPT (0.46) MAPTSMN1; SMN2POLBGAAMEN1
SCHEMBL13837780 0.83 MAPT (0.46) MAPTSMN1; SMN2POLBGAAMEN1
SCHEMBL4159465 0.82 CYP2C9 (0.55) MAPTSMN1; SMN2POLBGAAMEN1
SCHEMBL7330114 0.82 SMPD1 (0.54) MAPTSMN1; SMN2POLBGAAMEN1
SCHEMBL7322765 0.81 PDE4D (0.70) PDE4APDE4BPDE4CPDE4D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106146350-B A kind of new method of synthesizing amino formic acid oxime ester derivative 华南理工大学 2017-10-20 CN claimed
CN-106146350-A A kind of new method of synthesizing amino methylcarbamoyl oximino ester derivant 华南理工大学 2016-11-23 CN claimed
US-20240392220-A1 BRANDY REPLICAS AVA FOOD LABS, INC. 2024-11-28 US disclosed
EP-4408967-A1 BRANDY REPLICAS AVA FOOD LABS, INC. (US) 2024-08-07 EP disclosed
CN-118339274-A Brandy replica 艾娃食品实验室股份有限公司 2024-07-12 CN disclosed
WO-2023055801-A1 BRANDY REPLICAS AVA FOOD LABS, INC. (US) 2023-04-06 WO disclosed
CN-108794419-B Naphtho [2,3-b ] isoxazole-4, 9-diketone derivative and preparation method and application thereof 中南大学 2022-07-05 CN disclosed
US-10174033-B2 N6-substituted adenosine derivatives and N6-substituted adenine derivatives and uses thereof INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF MEDICAL SCIENCES (CN) 2019-01-08 US disclosed
CN-104382924-B N6 substituted adenosines derivative and N6 substituted adenines derivatives and application thereof 中国医学科学院药物研究所 2017-12-22 CN disclosed
CN-106146350-B A kind of new method of synthesizing amino formic acid oxime ester derivative 华南理工大学 2017-10-20 CN disclosed
CN-105037211-B A kind of threonyl amine carbamate derivative and application 南开大学 2017-08-18 CN disclosed
US-20020143027-A1 Novel substituted imides MULLER GEORGE W (US) 2002-10-03 US disclosed
US-6429221-B1 INHIBITORS OF TUMOR NECROSIS FACTOR; USED TO TREAT CACHEXIA, ENDOTOXIC SHOCK, AND RETROVIRUS REPLICATION CELGENE CORPORATION 2002-08-06 US disclosed
EP-0800514-A1 SUBSTITUTED IMIDES AS TNF INHIBITORS CELGENE CORPORATION (US) 1997-10-15 EP disclosed
WO-1996020926-A9 SUBSTITUTED IMIDES AS TNF INHIBITORS 1996-09-26 WO disclosed
WO-1996020926-A1 SUBSTITUTED IMIDES AS TNF INHIBITORS CELGENE CORPORATION (US) 1996-07-11 WO disclosed
EP-0538384-A4 OXAMIDES SMITHKLINE BEECHAM CORP (US) 1995-04-12 EP disclosed
US-5393788-A Phenylalkyl oxamides SMITHKLINE BEECHAM CORPORATION (US) 1995-02-28 US disclosed
EP-0538384-A1 OXAMIDES SMITHKLINE BEECHAM CORPORATION (US) 1993-04-28 EP disclosed
WO-1992000968-A1 OXAMIDES SMITHKLINE BEECHAM CORPORATION (US) 1992-01-23 WO 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-20020143027-A1 Novel substituted imides TNF, MIF, TNFRSF1A MAPT 4400/4885SMN1; SMN2 312/4885POLB 794/4885
US-10174033-B2 N6-substituted adenosine derivatives and N6-substituted adenine derivatives and uses thereof ADORA2A, ADORA3, ADORA1 MAPT 117/4885SMN1; SMN2 330/4885POLB 2416/4885

“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.