SCHEMBL477416

SCHEMBL477416

OC(c1ccccc1)C1CCCCC1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
IDO1 P14902 2/20 0.53
DHODH Q02127 1/20 0.53
KDM4E B2RXH2 2/20 0.51
CYP1A2 P05177 2/20 0.51
CYP2D6 P10635 2/20 0.51
CYP3A4 P08684 1/20 0.51
TSHR P16473 1/20 0.51
HTR2A P28223 1/20 0.51
HTR2C P28335 1/20 0.51
CARM1 Q86X55 1/20 0.49
PRMT6 Q96LA8 1/20 0.49
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
LMNA P02545 1/20 0.46
MAPT P10636 1/20 0.46
HTR1E P28566 1/20 0.46
S1PR3 Q99500 1/20 0.46
GAA P10253 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46
HRH3 Q9Y5N1 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
SCHEMBL1430742 1.00 IDO1 (0.53) IDO1DHODHKDM4ECYP1A2CYP2D6
SCHEMBL16995185 1.00 IDO1 (0.53) IDO1DHODHKDM4ECYP1A2CYP2D6
SCHEMBL477415 1.00 IDO1 (0.53) IDO1DHODHKDM4ECYP1A2CYP2D6
SCHEMBL8705439 0.98 KDM4E (0.53) IDO1DHODHKDM4ECYP1A2CYP2D6
SCHEMBL3310267 0.93 CYP1A2 (0.53) IDO1DHODHKDM4ECYP1A2CYP2D6
SCHEMBL477699 0.89 CYP1A2 (0.56) IDO1KDM4ECYP1A2CYP2D6CYP3A4
SCHEMBL19645377 0.89 CYP1A2 (0.56) IDO1KDM4ECYP1A2CYP2D6CYP3A4
SCHEMBL23652176 0.81 HRH3 (0.45) IDO1DHODHKDM4ECYP1A2CYP2D6
SCHEMBL8036930 0.81 DHODH (0.56) DHODHKDM4ETSHRKMT2AHRH3
SCHEMBL10021103 0.79 DHODH (0.58) IDO1DHODHCYP1A2TSHRMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106977368-A A kind of synthetic method of optical voidness phenylcyclohexyl methanol 康化(上海)新药研发有限公司 2017-07-25 CN claimed
EP-1042291-B1 ARYL-SUBSTITUTED PYRIDYLALKANE, ALKENE, AND ALKINE CARBOXAMIDES USEFUL AS CYTOSTATIC AND IMMUNOSUPPRESSIVE AGENTS KLINGE CO CHEM PHARM FAB (DE) 2005-07-13 EP claimed
JP-6032813-A None JP disclosed
US-11866430-B2 Naphthyridinone compounds useful as T cell activators BRISTOL-MYERS SQUIBB COMPANY (US) 2024-01-09 US disclosed
CN-112585139-B Naphthyridinone compounds as T cell activators 百时美施贵宝公司 2023-12-01 CN disclosed
US-20230271988-A1 METHOD FOR PRODUCING ORGANOMETALLIC NUCLEOPHILE AND REACTION METHOD USING ORGANOMETALLIC NUCLEOPHILE NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY (JP) 2023-08-31 US disclosed
US-20230271988-A1 METHOD FOR PRODUCING ORGANOMETALLIC NUCLEOPHILE AND REACTION METHOD USING ORGANOMETALLIC NUCLEOPHILE NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY (JP) 2023-08-31 US disclosed
EP-3814347-B1 NAPHTHYRIDINONE COMPOUNDS USEFUL AS T CELL ACTIVATORS BRISTOL MYERS SQUIBB CO (US) 2023-05-03 EP disclosed
EP-3814347-B1 NAPHTHYRIDINONE COMPOUNDS USEFUL AS T CELL ACTIVATORS BRISTOL MYERS SQUIBB CO (US) 2023-05-03 EP disclosed
WO-2023016459-A1 NOVEL ORGANIC ALKOXIDE AGGLOMERATE, AND PREPARATION METHOD THEREFOR AND APPLICATION AND THEREOF 上海科技大学 2023-02-16 WO disclosed
CN-109627152-B Photocatalytic synthesis method and application of cyclohexyl- (4-R phenyl) ketone compound 甘肃金盾化工有限责任公司 2022-01-25 CN disclosed
EP-0847988-A1 Process for the preparation of N-hydrocarbyl-substituted amides The Lubrizol Corporation (US) 1998-06-17 EP disclosed
EP-0846678-A1 Process for the preparation of N-hydrocarbyl-substituted amides The Lubrizol Corporation (US) 1998-06-10 EP disclosed
US-5712413-A Process for the preparation of N-hydrocarbyl-substituted amides such as tert-butylacrylamide via the Ritter reaction using solid heteropolyacid catalysts THE LUBRIZOL CORPORATION (US) 1998-01-27 US disclosed
US-5686424-A FOR TREATING INFLAMMATION MILES INC. (US) 1997-11-11 US disclosed
EP-0686635-A1 Pyridylthiazolidinecarboxylic acid amide derivatives, their preparation and their therapeutic uses Sankyo Company Limited (JP) 1995-12-13 EP disclosed
US-5470851-A Antihistamine, anticoagulants SANKYO COMPANY, LIMITED (JP) 1995-11-28 US disclosed
JP-H0632813-A POLYMERIZATION INITIATOR COMPOSITION THREE BOND CO LTD 1994-02-08 JP disclosed
EP-0564924-A2 2-Oxoethyl derivatives as immunosuppressants Bayer Corporation (US) 1993-10-13 EP disclosed
EP-0549364-A1 Pyridylthiazolidinecarboxylic acid amide derivatives, their preparation and their therapeutic uses Sankyo Company Limited (JP) 1993-06-30 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 (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-20230271988-A1 METHOD FOR PRODUCING ORGANOMETALLIC NUCLEOPHILE AND REACTION METHOD USING ORGANOMETALLIC NUCLEOPHILE HPD, TALDO1, OGG1 IDO1 2029/4885DHODH 313/4885KDM4E 1084/4885
US-11866430-B2 Naphthyridinone compounds useful as T cell activators DGKZ, DGKA, DGKG IDO1 1965/4885DHODH 557/4885KDM4E 2027/4885

“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.