Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1560135

Cl.NCCCC(NC(F)F)C(=O)O

nearest known ligand 0.45

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 Hydrochloric Acid. 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
ODC1 known ✓ P11926 1/20 0.35
FOLH1 Q04609 1/20 0.45
CPB2 Q96IY4 4/20 0.41
GSR P00390 1/20 0.39
RNPEP Q9H4A4 1/20 0.38
BLM P54132 2/20 0.38
LMNA P02545 2/20 0.38
KDM4E B2RXH2 1/20 0.38
MAPT P10636 1/20 0.38
RAB9A P51151 1/20 0.38
PMP22 Q01453 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
MMP2 P08253 1/20 0.37
MMP9 P14780 1/20 0.37
GGT1 P19440 1/20 0.36
SLC6A5 Q9Y345 1/20 0.35
NPSR1 Q6W5P4 1/20 0.34
GNPAT O15228 1/20 0.34
TGFBR1 P36897 1/20 0.33

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
Hydrochloric Acid SCHEMBL1560136 1.00 FOLH1 (0.45) FOLH1CPB2GSRRNPEPBLM
Hydrochloric Acid SCHEMBL21933053 0.98 FOLH1 (0.44) FOLH1CPB2GSRRNPEPBLM
SCHEMBL8734 0.98 FOLH1 (0.46) FOLH1CPB2GSRRNPEPBLM
SCHEMBL8735 0.98 FOLH1 (0.46) FOLH1CPB2GSRRNPEPBLM
SCHEMBL2873029 0.98 FOLH1 (0.46) FOLH1CPB2GSRRNPEPBLM
SCHEMBL6479470 0.92 FOLH1 (0.53) FOLH1CPB2GSRRNPEPMMP2
SCHEMBL6479474 0.92 FOLH1 (0.53) FOLH1CPB2GSRRNPEPMMP2
Ornithine SCHEMBL3820639 0.90 GSR (0.56) FOLH1GSR
Benzoquinone SCHEMBL28214836 0.87 FOLH1 (0.39) FOLH1CPB2GSRRNPEPMMP2
SCHEMBL7603037 0.83 FOLH1 (0.44) FOLH1CPB2GSRRNPEPBLM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2303288-A2 CONJUGATES OF A POLYMER, A BISPHOSPHONATE AND AN ANTI-ANGIOGENESIS AGENT AND USES THEREOF IN THE TREATMENT AND MONITORING OF BONE RELATED DISEASES Ramot at Tel-Aviv University Ltd. (IL) 2011-04-06 EP claimed
WO-2009141823-A2 CONJUGATES OF A POLYMER, A BISPHOSPHONATE AND AN ANTI-ANGIOGENESIS AGENT AND USES THEREOF IN THE TREATMENT AND MONITORING OF BONE RELATED DISEASES RAMOT AT TEL AVIV UNIVERSITY LTD. (IL) 2009-11-26 WO claimed
WO-2008157230-A1 RSK INHIBITORS AS ANTI-ANGIOGENIC THERAPEUTICS UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2008-12-24 WO claimed
CN-112481337-B High mannose glycoform content of regulatory ornithine metabolism to manipulate recombinant proteins 美国安进公司 2024-06-25 CN disclosed
WO-2023081681-A1 NITRIC OXIDE DONORS FOR USE IN SURGICAL RECOVERY BAXTER INTERNATIONAL INC. (US) 2023-05-11 WO disclosed
CN-115531555-A Application of mannose-modified nanoparticles in preparation of drug for treating osteosarcoma 上海市第一人民医院 2022-12-30 CN disclosed
CN-113072456-B Chiral alpha-difluoromethyl amino acid compound and preparation method thereof 中国科学技术大学 2022-04-19 CN disclosed
US-11254963-B2 Increasing ornithine accumulation to increase high mannose glycoform content of recombinant proteins AMGEN INC. (US) 2022-02-22 US disclosed
CN-112481337-A Modulation of ornithine metabolism to manipulate high mannose glycoform content of recombinant proteins 美国安进公司 2021-03-12 CN disclosed
CN-106029896-B Modulation of ornithine metabolism to manipulate high mannose glycoform content of recombinant proteins 美国安进公司 2020-10-27 CN disclosed
US-20200071738-A1 DECREASING ORNITHINE METABOLISM TO DECREASE THE HIGH MANNOSE GLYCOFORM CONTENT OF RECOMBINANT PROTEINS AMGEN INC. (US) 2020-03-05 US disclosed
EP-2303288-A2 CONJUGATES OF A POLYMER, A BISPHOSPHONATE AND AN ANTI-ANGIOGENESIS AGENT AND USES THEREOF IN THE TREATMENT AND MONITORING OF BONE RELATED DISEASES Ramot at Tel-Aviv University Ltd. (IL) 2011-04-06 EP disclosed
WO-2009141823-A2 CONJUGATES OF A POLYMER, A BISPHOSPHONATE AND AN ANTI-ANGIOGENESIS AGENT AND USES THEREOF IN THE TREATMENT AND MONITORING OF BONE RELATED DISEASES RAMOT AT TEL AVIV UNIVERSITY LTD. (IL) 2009-11-26 WO disclosed
WO-2009141826-A2 NOVEL CONJUGATES OF POLYMERS HAVING A THERAPEUTICALLY ACTIVE AGENT AND AN ANGIOGENESIS TARGETING MOIETY ATTACHED THERETO AND USES THEREOF IN THE TREATMENT OF ANGIOGENESIS RELATED DISEASES RAMOT AT TEL AVIV UNIVERSITY LTD. (IL) 2009-11-26 WO disclosed
WO-2008157230-A1 RSK INHIBITORS AS ANTI-ANGIOGENIC THERAPEUTICS UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2008-12-24 WO disclosed
US-7045550-B2 Polyamines and analogs for protecting cells during cancer chemotherapy and radiotherapy WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2006-05-16 US disclosed
US-20030118539-A1 Polyamines and analogs for protecting cells during cancer chemotherapy and radiotherapy WISCONSIN ALUMNI RESEARCH FOUNDATION 2003-06-26 US disclosed
WO-2003013245-A1 POLYAMINES AND ANALOGS FOR PROTECTING CELLS DURING CANCER CHEMOTHERAPY AND RADIOTHERAPY WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2003-02-20 WO disclosed
EP-1278537-A2 METHODS FOR STIMULATING NERVOUS SYSTEM REGENERATION AND REPAIR BY REGULATING ARGINASE I AND POLYAMINE SYNTHESIS The Research Foundation of the City University of New York (US) 2003-01-29 EP disclosed
WO-2001085981-A2 METHODS FOR STIMULATING NERVOUS SYSTEM REGENERATION AND REPAIR BY REGULATING ARGINASE I AND POLYAMINE SYNTHESIS RESEARCH FOUNDATION OF CITY UNIVERSITY OF NEW YORK (US) 2001-11-15 WO disclosed