SCHEMBL1325541

SCHEMBL1325541

CCCCCC1C(=O)c2ccccc2C1=O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 2/20 0.44
MEN1 O00255 1/20 0.44
NPC1 O15118 1/20 0.44
POLB P06746 1/20 0.44
GAA P10253 1/20 0.44
KMT2A Q03164 1/20 0.44
ALDH1A1 P00352 4/20 0.43
HPGD P15428 2/20 0.43
KDM4E B2RXH2 1/20 0.43
PTPN1 P18031 1/20 0.42
ALDH2 P05091 1/20 0.42
ALDH3A1 P30838 1/20 0.42
CYP3A4 P08684 2/20 0.41
LMNA P02545 1/20 0.41
CYP1A2 P05177 1/20 0.41
CYP2C9 P11712 1/20 0.41
MAPK1 P28482 1/20 0.41
CYP2C19 P33261 1/20 0.41
TP53 P04637 1/20 0.41
MAPT P10636 1/20 0.41

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
SCHEMBL15845072 0.96 PTPN1 (0.44) RAB9AMEN1NPC1POLBGAA
SCHEMBL15844488 0.96 PTPN1 (0.44) RAB9AMEN1NPC1POLBGAA
SCHEMBL11884237 0.89 ALDH1A1 (0.40) RAB9AMEN1NPC1KMT2AALDH1A1
SCHEMBL22845855 0.79 GSK3B (0.42) RAB9AMEN1NPC1POLBGAA
SCHEMBL28085412 0.78 PTPN1 (0.40) PTPN1
SCHEMBL28240950 0.78 PTPN1 (0.40) PTPN1
SCHEMBL8365427 0.78 ALDH1A1 (0.58) RAB9AMEN1NPC1POLBGAA
SCHEMBL877438 0.77 HTR2A (0.56)
SCHEMBL30006748 0.76 PTPN1 (0.44) PTPN1
SCHEMBL6060915 0.75 HTR2A (0.54)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114737210-B Method for continuously preparing 1,3-indenone spiro imidazoline compound by using electrochemical microchannel reaction device 南京工业大学 2023-04-18 CN claimed
CN-114737210-A Method for continuously preparing 1, 3-indene diketone spiroimidazoline compound by using electrochemical microchannel reaction device 南京工业大学 2022-07-12 CN claimed
JP-60130521-A None JP disclosed
JP-60130569-A None JP disclosed
EP-3611158-B1 1,3-DI-OXO-INDENE DERIVATIVE, PHARMACEUTICALLY ACCEPTABLE SALT OR OPTICAL ISOMER THEREOF, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AS AN ANTIVIRAL, ACTIVE INGREDIENT KOREA RES INST CHEMICAL TECH (KR) 2023-12-20 EP disclosed
US-20230255995-A1 Nicotinyl Riboside Compounds and Their Uses MITOPOWER LLC 2023-08-17 US disclosed
EP-3986420-A1 NICOTINYL RIBOSIDE COMPOUNDS AND THEIR USES Mitopower LLC (US) 2022-04-27 EP disclosed
US-20200397807-A1 NICOTINYL RIBOSIDE COMPOUNDS AND THEIR USES MITOPOWER LLC 2020-12-24 US disclosed
WO-2020257283-A1 NICOTINYL RIBOSIDE COMPOUNDS AND THEIR USES MITOPOWER LLC (US) 2020-12-24 WO disclosed
EP-2722322-B1 1,3-DI-OXO-INDENE DERIVATIVE, PHARMACEUTICALLY ACCEPTABLE SALT OR OPTICAL ISOMER THEREOF, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AS AN ANTIVIRAL, ACTIVE INGREDIENT KOREA RES INST CHEMICAL TECH (KR) 2019-06-12 EP disclosed
US-9796753-B2 N-substituted indenoisoquinolines and syntheses thereof PURDUE RESEARCH FOUNDATION (US) 2017-10-24 US disclosed
JP-S60130521-A ANTICANCER AGENT MORISHITA SEIYAKU KK 1985-07-12 JP disclosed
EP-0138272-A1 Diarylindane-1,3-diones, their preparation and use AKZO N.V. (NL) 1985-04-24 EP disclosed
EP-0138272-A1 Diarylindane-1,3-diones, their preparation and use AKZO N.V. (NL) 1985-04-24 EP disclosed
EP-0008540-B1 2-ARYL-1,3-INDANDIONE DERIVATIVES AND COMPOSITIONS COMPRISING THEM FOR CONTROLLING ECTOPARASITIC ACARINA UNION CARBIDE CORPORATION (US) 1984-10-24 EP disclosed
US-4386086-A ENOL DERIVATIVES OF 2-ARYL-1,3-INDANDIONES UNION CARBIDE CORPORATION (US) 1983-05-31 US disclosed
US-4338122-A MITICIDES, HERBICIDES UNION CARBIDE CORPORATION (US) 1982-07-06 US disclosed
US-4260776-A PYRAZOLONE BAYER AKTIENGESELLSCHAFT (DE) 1981-04-07 US disclosed
EP-0008540-A2 2-aryl-1,3-indandione derivatives and compositions comprising them for controlling ectoparasitic acarina UNION CARBIDE CORPORATION (US) 1980-03-05 EP disclosed
EP-0008540-A2 2-aryl-1,3-indandione derivatives and compositions comprising them for controlling ectoparasitic acarina UNION CARBIDE CORPORATION (US) 1980-03-05 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-20200397807-A1 NICOTINYL RIBOSIDE COMPOUNDS AND THEIR USES NADK, NNT, NAMPT RAB9A 1616/4885MEN1 3810/4885NPC1 798/4885
US-20230255995-A1 Nicotinyl Riboside Compounds and Their Uses NADK, NNT, NAMPT RAB9A 1616/4885MEN1 3810/4885NPC1 798/4885

“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.