SCHEMBL7780927

SCHEMBL7780927

CC(=O)Nc1cccc2c(-c3c(P(c4ccccc4)c4ccccc4)ccc4c(NC(C)=O)cccc34)c(P(c3ccccc3)c3ccccc3)ccc12

nearest known ligand 0.51

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ RXFP1 Q9HBX9 1/20 0.51
▸ KMT2A Q03164 2/20 0.46
▸ MEN1 O00255 1/20 0.44
▸ CASP6 P55212 1/20 0.44
▸ ALDH1A1 P00352 3/20 0.43
▸ HPGD P15428 2/20 0.43
▸ KDM4E B2RXH2 2/20 0.43
▸ MAPT P10636 1/20 0.43
▸ MAOA P21397 1/20 0.42
▸ POLB P06746 2/20 0.42
▸ CYP2C19 P33261 1/20 0.42
▸ MAPK1 P28482 1/20 0.41
▸ GAA P10253 1/20 0.40
▸ PARP14 Q460N5 3/20 0.40
▸ PKM P14618 1/20 0.40
▸ GPR35 Q9HC97 1/20 0.39

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
SCHEMBL6053373 0.81 RXFP1 (0.46) RXFP1KMT2ACASP6ALDH1A1HPGD
SCHEMBL29230461 0.78 ALDH1A1 (0.53) KMT2AALDH1A1HPGDKDM4EMAPT
SCHEMBL1900214 0.78 RXFP1 (0.66) RXFP1KMT2AMEN1CASP6ALDH1A1
SCHEMBL30842828 0.73 ALDH1A1 (0.48) ALDH1A1HPGDKDM4EMAPTMAOA
Acetic Acid SCHEMBL4438549 0.72 WDR5 (0.49) ALDH1A1HPGDKDM4EMAPTGAA
SCHEMBL8982554 0.72 KDM4E (0.63) RXFP1KMT2AMEN1CASP6ALDH1A1
SCHEMBL14596146 0.72 CYP3A4 (0.39) RXFP1KMT2AMEN1
SCHEMBL25946008 0.72 RXFP1 (0.80) RXFP1KMT2AMEN1CASP6ALDH1A1
SCHEMBL30881878 0.72 RXFP1 (0.80) RXFP1KMT2AMEN1CASP6ALDH1A1
SCHEMBL357522 0.71 KDM4E (0.69) RXFP1KMT2AMEN1CASP6ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0258967-B2 Process for producing optically active alcohols TAKASAGO PERFUMERY CO LTD (JP) 1996-08-21 — — EP claimed
EP-0245960-B1 PROCESS FOR PREPARING N-ACYLTETRAHYDROISOQUINOLINE Takasago Perfumery Co., Ltd. (JP) 1992-07-29 — — EP claimed
EP-0272787-B1 CATALYTIC PRODUCTION OF OPTICALLY ACTIVE CARBOXYLIC ACID Takasago International Corporation (JP) 1992-05-06 — — EP claimed
US-4962230-A RUTHENIUM-OPTICALLY ACTIVE PHOSPHINE COMPLEX HYDROGENATION CATALYST TAKASAGO INTERNATIONAL CORPORATION (JP) 1990-10-09 — — US claimed
US-4851537-A Process for preparing N-acyltetrahydroisoquinoline TAKASAGO PERFUMERY CO., LTD. (JP) 1989-07-25 — — US claimed
EP-0272787-A2 Catalytic production of optically active carboxylic acid Takasago International Corporation (JP) 1988-06-29 — — EP claimed
EP-0258967-A2 Process for producing optically active alcohols Takasago Perfumery Co., Ltd. (JP) 1988-03-09 — — EP claimed
EP-0855390-B1 A process for producing optically active pyrrolidine derivatives TAKASAGO PERFUMERY CO LTD (JP) 2001-10-04 — — EP disclosed
US-5942629-A HYDROGENATING 3-ACETYL-1-BENZYL-2-PYRROLIDINONE IN PRESENCE OF A COMPLEX FORMED FROM BIDENTATE PHOSPHINE AND RUTHENIUM CATALYST TO PRODUCE INTERMEDIATE, REDUCING THE INTERMEDIATE, MESYLATING OR TOSYLATING THE PRODUCT, FINALLY METHYLAMINATING TAKASAGO INTERNATIONAL CORPORATION (JP) 1999-08-24 — — US disclosed
EP-0855390-A1 A process for producing optically active pyrrolidine derivatives Takasago International Corporation (JP) 1998-07-29 — — EP disclosed
US-5587510-A ASYMMETRICAL HYDROGENATION USING RUTHENIUM-PHOPSHINE COMPLEX AS CATALYSTS TAKASAGO INTERNATIONAL CORPORATION (JP) 1996-12-24 — — US disclosed
EP-0258967-B2 Process for producing optically active alcohols TAKASAGO PERFUMERY CO LTD (JP) 1996-08-21 — — EP disclosed
US-5204460-A Reacting azetidinone compound with acetic acid and oxidizing agent in the presence of ruthenium catalyst TAKASAGO INTERNATIONAL CORPORATION (JP) 1993-04-20 — — US disclosed
EP-0272787-B1 CATALYTIC PRODUCTION OF OPTICALLY ACTIVE CARBOXYLIC ACID Takasago International Corporation (JP) 1992-05-06 — — EP disclosed
US-4851537-A Process for preparing N-acyltetrahydroisoquinoline TAKASAGO PERFUMERY CO., LTD. (JP) 1989-07-25 — — US disclosed
EP-0272787-A2 Catalytic production of optically active carboxylic acid Takasago International Corporation (JP) 1988-06-29 — — EP disclosed
EP-0258967-A2 Process for producing optically active alcohols Takasago Perfumery Co., Ltd. (JP) 1988-03-09 — — EP disclosed
US-4705895-A METAL COMPLEXES AS ASYMMETRIC SYNTHESES TAKASAGO PERFUMERY CO., LTD. (JP) 1987-11-10 — — US disclosed
US-4705895-A METAL COMPLEXES AS ASYMMETRIC SYNTHESES TAKASAGO PERFUMERY CO., LTD. (JP) 1987-11-10 — — US disclosed
EP-0235450-A1 Phosphine compounds for complex catalysts for asymmetric syntheses Takasago Perfumery Co., Ltd. (JP) 1987-09-09 — — EP disclosed
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