Histidine

Histidine

SCHEMBL209483

Cl.N[C@@H](Cc1c[nH]cn1)C(=O)O

nearest known ligand 0.46

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 Histidine. 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
PTGS1 known ✓ P23219 1/20 0.42
SLC7A5 Q01650 3/20 0.46
CYP3A4 P08684 2/20 0.46
CYP1A2 P05177 1/20 0.45
PKM P14618 3/20 0.42
ALPI P09923 1/20 0.42
XIAP P98170 1/20 0.42
GRIA2 P42262 4/20 0.40
GRIA1 P42261 3/20 0.40
GRIA3 P42263 3/20 0.40
GRIA4 P48058 3/20 0.40
HSD17B10 Q99714 2/20 0.39
KDM4E B2RXH2 2/20 0.39
MEN1 O00255 2/20 0.39
LMNA P02545 2/20 0.39
MAPT P10636 2/20 0.39
BLM P54132 2/20 0.39
PMP22 Q01453 2/20 0.39
KMT2A Q03164 2/20 0.39
HIF1A Q16665 2/20 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
Histidine SCHEMBL27153440 1.00 SLC7A5 (0.46) SLC7A5CYP3A4CYP1A2PKMALPI
Histidine SCHEMBL94550 1.00 SLC7A5 (0.46) SLC7A5CYP3A4CYP1A2PKMALPI
Histidine SCHEMBL30286660 1.00 SLC7A5 (0.46) SLC7A5CYP3A4CYP1A2PKMALPI
Histidine SCHEMBL16893958 1.00 SLC7A5 (0.46) SLC7A5CYP3A4CYP1A2PKMALPI
D-Histidine SCHEMBL8002457 1.00 SLC7A5 (0.46) SLC7A5CYP3A4CYP1A2PKMALPI
Histidine SCHEMBL139654 1.00 SLC7A5 (0.46) SLC7A5CYP3A4CYP1A2PKMALPI
Histidine SCHEMBL670490 1.00 SLC7A5 (0.46) SLC7A5CYP3A4CYP1A2PKMALPI
Histidine SCHEMBL3985696 1.00 SLC7A5 (0.46) SLC7A5CYP3A4CYP1A2PKMALPI
Histidine SCHEMBL16893957 1.00 SLC7A5 (0.46) SLC7A5CYP3A4CYP1A2PKMALPI
Histidine SCHEMBL3985692 1.00 SLC7A5 (0.46) SLC7A5CYP3A4CYP1A2PKMALPI

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

Appears in 11612 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-121490076-B Stable anti-human MASP2 monoclonal antibody preparation Shanghai Maiji Pharmaceutical Co.,Ltd. (CN) 2026-05-26 CN claimed
CN-122095249-A Development of high throughput assays for identifying al3+ traces in biopharmaceutical products 2026-05-26 CN claimed
CN-122081234-A Low-serum MSB1 suspension medium and chicken infectious anemia virus inactivated vaccine 2026-05-26 CN claimed
CN-121379932-B Culture medium for high-density serum-free suspension culture of BHK-21 cells and application thereof Zhongsheng tianxinhe (Wuxi) Biotechnology Co.,Ltd. (CN) 2026-05-26 CN claimed
WO-2026102693-A1 PCSK9 ANTIBODY AND USE THEREOF 北京天广实生物技术股份有限公司 2026-05-21 WO claimed
US-20260139045-A1 STABILIZED FORMULATIONS CONTAINING ANTI-ANGPTL3 ANTIBODIES REGENERON PHARMACEUTICALS INC (US) 2026-05-21 US claimed
WO-2026106498-A1 PERFUSION FLUID, METHODS OF PRODUCING PERFUSION FLUID, AND ITS USES NanoSanguis S.A. (PL) 2026-05-21 WO claimed
US-20260139047-A1 PHARMACEUTICAL COMPOSITION CONTAINING FUSION PROTEIN JIANGSU HENGRUI PHARMACEUTICALS CO LTD (CN) 2026-05-21 US claimed
EP-4744487-A1 FLUID, METHODS OF PRODUCING FLUID, AND ITS USES NanoSanguis S.A. (PL) 2026-05-20 EP claimed
EP-4566674-B1 ANTIBODY COMPOSITIONS AND METHODS OF USE THEREOF BRISTOL MYERS SQUIBB CO (US) 2026-05-20 EP claimed
EP-0336987-A1 Feed additive for ruminants MITSUBISHI KASEI CORPORATION (JP) 1989-10-18 EP claimed
US-4864031-A Process for the resolution of D,L-racemic mixtures YEDA RESEARCH AND DEVELOPMENT CO., LTD. (IL) 1989-09-05 US claimed
US-4600708-A MASKING TASTE OR ANESTHESIA CHARACTERISTICS USING AMINO ACID OR LECITHIN AMERICAN HOME PRODUCTS CORPORATION (US) 1986-07-15 US claimed
EP-0054635-B1 PROTECTIVE SOLUTION FOR HEART AND KIDNEY, AND MANUFACTURING PROCESS Dr. Franz Köhler Chemie GmbH (DE) 1985-02-13 EP claimed
US-4415556-A ANTIISCHEMIC AGENTS CONTAINING ALPHA-KETOGLUTARIC ACID; SURGERY; TRANSPLANTS DR. FRANZ KOHLER CHEMIE GMBH (DE) 1983-11-15 US claimed
US-4390722-A CRYSTALLIZATION FROM SUPERSATURATED SOLUTION USING AMINO ACID AS AS CRYSTAL INHIBITOR YEDA RESEARCH AND DEVELOPMENT COMPANY LTD. (IL) 1983-06-28 US claimed
EP-0012272-B1 PROTECTING SOLUTION FOR HEART AND KIDNEYS AND PROCESS FOR ITS MANUFACTURE Dr. Franz Köhler Chemie KG (DE) 1981-12-30 EP claimed
EP-0008171-B1 HAIR TREATMENT COMPOSITION AND METHOD UNILEVER PLC (GB) 1981-11-11 EP claimed
EP-0012272-A1 Protecting solution for heart and kidneys and process for its manufacture Dr. Franz Köhler Chemie KG (DE) 1980-06-25 EP claimed
US-4035513-A COSMETICS SHISEIDO CO., LTD. (JA) 1977-07-12 US claimed