Nitroanilide

Nitroanilide

SCHEMBL5331152

Cl.Cl.O=[N+]([O-])Nc1ccccc1

nearest known ligand 0.48

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA known ✓ P10253 2/20 0.41
CA2 known ✓ P00918 1/20 0.41
PTGS1 known ✓ P23219 1/20 0.38
SLC6A2 known ✓ P23975 1/20 0.38
PTGS2 known ✓ P35354 1/20 0.38
HTR2B known ✓ P41595 1/20 0.38
L3MBTL1 Q9Y468 5/20 0.48
ALOX12 P18054 2/20 0.48
HPGD P15428 1/20 0.48
ALDH1A1 P00352 10/20 0.45
TDP1 Q9NUW8 3/20 0.45
MAPK1 P28482 3/20 0.45
CASP7 P55210 1/20 0.45
MAPT P10636 5/20 0.44
LMNA P02545 4/20 0.44
MEN1 O00255 4/20 0.41
KMT2A Q03164 4/20 0.41
CXCR2 P25025 1/20 0.41
CA12 O43570 1/20 0.41
CA9 Q16790 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
Nitroanilide SCHEMBL3094185 1.00 L3MBTL1 (0.48) L3MBTL1ALOX12HPGDALDH1A1TDP1
Nitroanilide SCHEMBL5718352 0.97 L3MBTL1 (0.50) L3MBTL1ALOX12HPGDALDH1A1TDP1
Nitroanilide SCHEMBL6001 0.97 L3MBTL1 (0.50) L3MBTL1ALOX12HPGDALDH1A1TDP1
Nitroanilide SCHEMBL28530795 0.95 L3MBTL1 (0.48) L3MBTL1ALOX12HPGDALDH1A1TDP1
Nitroanilide SCHEMBL29021277 0.95 L3MBTL1 (0.48) L3MBTL1ALOX12HPGDALDH1A1TDP1
Nitroanilide SCHEMBL28115452 0.95 L3MBTL1 (0.48) L3MBTL1ALOX12HPGDALDH1A1TDP1
Nitroanilide SCHEMBL30436028 0.95 L3MBTL1 (0.48) L3MBTL1ALOX12HPGDALDH1A1TDP1
Nitroanilide SCHEMBL4541850 0.95 L3MBTL1 (0.48) L3MBTL1ALOX12HPGDALDH1A1TDP1
Nitroanilide SCHEMBL20876421 0.95 L3MBTL1 (0.48) L3MBTL1ALOX12HPGDALDH1A1TDP1
Nitroanilide SCHEMBL29195338 0.95 L3MBTL1 (0.48) L3MBTL1ALOX12HPGDALDH1A1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4507716-A1 METHODS OF PREPARING ALBUMIN PREPARATIONS CSL Behring LLC (US) 2025-02-19 EP disclosed
WO-2023200908-A1 METHODS OF PREPARING ALBUMIN PREPARATIONS CSL BEHRING LLC (US) 2023-10-19 WO disclosed
CN-108424474-B Deanticoagulated heparin derivatives and their use in the treatment of inflammatory bowel disease 清华大学 2023-07-25 CN disclosed
CN-115541513-A Method for detecting plasmin content in dairy product 新希望乳业股份有限公司 2022-12-30 CN disclosed
EP-3016971-A1 COMPOSITIONS AND METHODS FOR INHIBITING THROMBOGENESIS National University of Singapore (SG) 2016-05-11 EP disclosed
WO-2015002611-A9 COMPOSITIONS AND METHODS FOR INHIBITING THROMBOGENESIS NATIONAL UNIVERSITY OF SINGAPORE (SG) 2016-02-25 WO disclosed
WO-2015002611-A1 COMPOSITIONS AND METHODS FOR INHIBITING THROMBOGENESIS NATIONAL UNIVERSITY OF SINGAPORE (SG) 2015-01-08 WO disclosed
WO-2007050072-A1 SALIVA TEST FOR HEMOLYTIC STREPTOCOCCUS MOSHER LEROY E (US) 2007-05-03 WO disclosed
WO-1995002066-A1 METHOD FOR INHIBITING PROCOAGULANT HLA-DR OF MELANOMA CELLS BIOMIDE INVESTMENT LIMITED PARTNERSHIP (US) 1995-01-19 WO disclosed
WO-1989009817-A1 COMPOSITION AND METHOD FOR ACCELERATION OF CLOT LYSIS THE GENERAL HOSPITAL CORPORATION (US) 1989-10-19 WO disclosed
EP-0336693-A2 Acceleration of clot lysis THE GENERAL HOSPITAL CORPORATION (US) 1989-10-11 EP disclosed