Cpp-115 Free Base

Cpp-115 Free Base

SCHEMBL14687433

Cl.N[C@H]1C[C@@H](C(=O)O)CC1=C(F)F

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Cpp-115 Free Base. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
ABAT P80404 3/20 0.96
OAT P04181 1/20 0.64
GABRR1 P24046 1/20 0.37
SLC6A12 P48065 1/20 0.32
SLC6A11 P48066 1/20 0.32
SLC6A13 Q9NSD5 1/20 0.32
PLG P00747 1/20 0.31
PLAT P00750 1/20 0.31
LMNA P02545 1/20 0.31

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
Cpp-115 Free Base SCHEMBL15142226 1.00 ABAT (0.96) ABATOATGABRR1SLC6A12SLC6A11
Cpp-115 Free Base SCHEMBL2411394 0.98 ABAT (1.00) ABATOATGABRR1SLC6A12SLC6A11
Cpp-115 Free Base SCHEMBL21404893 0.98 ABAT (1.00) ABATOATGABRR1SLC6A12SLC6A11
Cpp-115 Free Base SCHEMBL12258069 0.98 ABAT (1.00) ABATOATGABRR1SLC6A12SLC6A11
Cpp-115 Free Base SCHEMBL2408171 0.98 ABAT (1.00) ABATOATGABRR1SLC6A12SLC6A11
Cpp-115 Free Base SCHEMBL2407298 0.98 ABAT (1.00) ABATOATGABRR1SLC6A12SLC6A11
Hydrochloric Acid SCHEMBL22440735 0.80 OAT (0.97) ABATOATGABRR1
SCHEMBL17742869 0.80 ABAT (0.69) ABATOATGABRR1SLC6A12SLC6A11
SCHEMBL29318645 0.79 ABAT (0.68) ABATOATGABRR1PLGPLAT
SCHEMBL29317652 0.79 ABAT (0.68) ABATOATGABRR1PLGPLAT

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160151316-A1 METHOD OF TREATING TOURETTE'S DISORDER WITH GABA-AMINOTRANSFERASE INACTIVATORS CATALYST PHARMACEUTICAL PARTNERS 2016-06-02 US disclosed
US-20160151316-A1 METHOD OF TREATING TOURETTE'S DISORDER WITH GABA-AMINOTRANSFERASE INACTIVATORS CATALYST PHARMACEUTICAL PARTNERS 2016-06-02 US disclosed
US-9254274-B2 Method of treating Tourette'S disorder with GABA-aminotransferase inactivators CATALYST PHARMACEUTICAL PARTNERS, INC. (US) 2016-02-09 US disclosed
US-9254274-B2 Method of treating Tourette'S disorder with GABA-aminotransferase inactivators CATALYST PHARMACEUTICAL PARTNERS, INC. (US) 2016-02-09 US disclosed
US-8969413-B2 Methods of using (1S,3S)-3-amino-4-difluoromethylenyl-1-cyclopentanoic acid CATALYST PHARMACEUTICAL PARTNERS (US) 2015-03-03 US disclosed
EP-2806867-A1 METHOD OF TREATING TOURETTE'S DISORDER WITH GABA-AMINOTRANSFERASE INACTIVATORS Catalyst Pharmaceutical Partners, Inc. (US) 2014-12-03 EP disclosed
EP-2806867-A1 METHOD OF TREATING TOURETTE'S DISORDER WITH GABA-AMINOTRANSFERASE INACTIVATORS Catalyst Pharmaceutical Partners, Inc. (US) 2014-12-03 EP disclosed
US-8895313-B2 Ligands for aggregated tau molecules WISTA LABORATORIES LTD. (SG) 2014-11-25 US disclosed
US-20140336256-A1 METHOD OF TREATING TOURETTE'S DISORDER WITH GABA-AMINOTRANSFERASE INACTIVATORS CATALYST PHARMACEUTICAL PARTNERS 2014-11-13 US disclosed
US-20140336256-A1 METHOD OF TREATING TOURETTE'S DISORDER WITH GABA-AMINOTRANSFERASE INACTIVATORS CATALYST PHARMACEUTICAL PARTNERS 2014-11-13 US disclosed
WO-2013112363-A1 METHOD OF TREATING TOURETTE'S DISORDER WITH GABA-AMINOTRANSFERASE INACTIVATORS CATALYST PHARMACEUTICAL PARTNERS (US) 2013-08-01 WO disclosed
WO-2013112363-A1 METHOD OF TREATING TOURETTE'S DISORDER WITH GABA-AMINOTRANSFERASE INACTIVATORS CATALYST PHARMACEUTICAL PARTNERS (US) 2013-08-01 WO disclosed
US-20130041028-A1 METHODS OF USING (1S,3S)-3-AMINO-4-DIFLUOROMETHYLENYL-1-CYCLOPENTANOIC ACID NORTHWESTERN UNIVERSITY (US) 2013-02-14 US disclosed