L-Nil

L-Nil

SCHEMBL677147

CC(=N)NCCCC[C@H](N)C(=O)O.Cl.Cl

nearest known ligand 0.51

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 L-Nil. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ARG2 P78540 4/20 0.51
NOS2 P35228 6/20 0.50
NOS1 P29475 5/20 0.50
BLM P54132 1/20 0.50
ARG1 P05089 3/20 0.49
GSR P00390 1/20 0.48
OTC P00480 1/20 0.47
NOS3 P29474 4/20 0.47
CYP1A2 P05177 1/20 0.47
CYP3A4 P08684 1/20 0.47
TSHR P16473 1/20 0.47
DPP7 Q9UHL4 1/20 0.45
MEN1 O00255 1/20 0.45
CYP2C19 P33261 1/20 0.45
KMT2A Q03164 1/20 0.45
GGT1 P19440 1/20 0.43
GNAI3 P08754 1/20 0.43
GNAO1 P09471 1/20 0.43
GNAI1 P63096 1/20 0.43

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
L-Nil SCHEMBL1321685 1.00 ARG2 (0.51) ARG2NOS2NOS1BLMARG1
L-Nil SCHEMBL7974005 1.00 ARG2 (0.51) ARG2NOS2NOS1BLMARG1
L-Nil SCHEMBL7977021 1.00 ARG2 (0.51) ARG2NOS2NOS1BLMARG1
Hydrochloric Acid SCHEMBL8470176 0.98 ARG2 (0.50) ARG2NOS2NOS1BLMARG1
L-Nil SCHEMBL31540966 0.98 ARG2 (0.50) ARG2NOS2NOS1BLMARG1
L-Nil SCHEMBL934874 0.98 ARG2 (0.50) ARG2NOS2NOS1BLMARG1
L-Nil SCHEMBL322091 0.98 ARG2 (0.50) ARG2NOS2NOS1BLMARG1
SCHEMBL8065968 0.97 NOS2 (0.50) ARG2NOS2NOS1BLMARG1
L-Nio SCHEMBL676368 0.95 OTC (0.53) ARG2NOS2NOS1BLMARG1
L-Nio SCHEMBL1320520 0.95 OTC (0.53) ARG2NOS2NOS1BLMARG1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1171861-C halogenated amidino amino acid derivatives useful as nitric oxide synthase inhibitors GD 2004-10-20 CN claimed
CN-1292779-A Haloamidino amino acid derivatives as nitric oxide synthase inhibitors SEARLE & CO (US) 2001-04-25 CN claimed
US-20240041869-A1 OPHTHALMIC COMPOSITION COMPRISING AN ANTI-ALLERGEN AND A REDNESS REDUCTION AGENT BAUSCH + LOMB IRELAND LIMITED (IE) 2024-02-08 US disclosed
US-9522163-B2 Methods of treating hepatitis University of Pittsburgh—of the Commonwealth System of Higher Education (US) 2016-12-20 US disclosed
EP-2515917-B1 BRIMONIDINE FOR EYE WHITENING EYE THERAPIES LLC (US) 2015-10-07 EP disclosed
US-8765758-B2 Compositions and methods for eye whitening EYE THERAPIES LLC (US) 2014-07-01 US disclosed
US-20140141103-A1 METHODS OF TREATING HEPATITIS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2014-05-22 US disclosed
US-20130202720-A1 METHODS OF TREATING HEPATITIS BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2013-08-08 US disclosed
WO-2012149381-A1 COMPOSITIONS AND METHODS FOR IMPROVING NIGHT VISION Alpha Synergy Development, Inc. (US) 2012-11-01 WO disclosed
US-20120276220-A1 Method of Treating Hepatitis YALE UNIVERSITY (US) 2012-11-01 US disclosed
US-20120277239-A1 Compositions and Methods for Improving Night Vision ALPHA SYNERGY DEVELOPMENT INC. (US) 2012-11-01 US disclosed
US-20110160214-A1 Compositions and methods for eye whitening Alpha Synergy Development, Inc. 2011-06-30 US disclosed
US-20110003823-A1 Compositions and methods for treatment of diseases and conditions associated with vasodilation and/or vascular leakage Alpha Synergy Development, Inc. 2011-01-06 US disclosed
US-20080171021-A1 PHARMACEUTICAL USE OF NITRIC OXIDE, HEME OXYGENASE-1 AND PRODUCTS OF HEME DEGRADATION BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2008-07-17 US disclosed
CN-1171861-C halogenated amidino amino acid derivatives useful as nitric oxide synthase inhibitors GD 2004-10-20 CN disclosed
US-20040131703-A1 Pharmaceutical use of nitric oxide, heme oxygenase-1 and products of heme degradation NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2004-07-08 US disclosed
US-20040052866-A1 Methods of treating hepatitis PITTSBURGH OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION, UNIVERSITY OF 2004-03-18 US disclosed
US-20040043992-A1 Meloxicam for alleviating organ injury during organ operation or transplantation BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2004-03-04 US disclosed
WO-2003097066-A1 USE OF MELOXICAM FOR ALLEVIATING ORGAN INJURY DURING ORGAN OPERATION OR TRANSPLANTATION BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2003-11-27 WO disclosed
CN-1292779-A Haloamidino amino acid derivatives as nitric oxide synthase inhibitors SEARLE & CO (US) 2001-04-25 CN disclosed