Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8975909

Cl.O=[N+]([O-])c1cccc(S(=O)(=O)O)c1

nearest known ligand 0.70

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 20)

geneUniProtsupporting neighboursconfidence
GAA known ✓ P10253 1/20 0.70
CA2 known ✓ P00918 3/20 0.66
MMP1 known ✓ P03956 1/20 0.65
MMP8 known ✓ P22894 1/20 0.65
MMP13 known ✓ P45452 1/20 0.65
CYP19A1 known ✓ P11511 1/20 0.53
KMT2A Q03164 3/20 0.70
HTT P42858 1/20 0.70
CA5A P35218 1/20 0.66
MMP2 P08253 2/20 0.65
CA1 P00915 1/20 0.65
MMP9 P14780 1/20 0.65
F2 P00734 3/20 0.59
PRSS1 P07477 3/20 0.59
PRSS2 P07478 3/20 0.59
PRSS3 P35030 3/20 0.59
LMNA P02545 2/20 0.59
MEN1 O00255 2/20 0.58
ALDH1A1 P00352 4/20 0.58
TSHR P16473 2/20 0.57

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 SCHEMBL8975904 1.00 KMT2A (0.70) KMT2AGAAHTTCA2CA5A
SCHEMBL6525363 0.98 KMT2A (0.72) KMT2AGAAHTTCA2CA5A
SCHEMBL33350 0.98 KMT2A (0.72) KMT2AGAAHTTCA2CA5A
SCHEMBL33351 0.98 KMT2A (0.72) KMT2AGAAHTTCA2CA5A
SCHEMBL9471995 0.98 KMT2A (0.72) KMT2AGAAHTTCA2CA5A
Nitrogen SCHEMBL4382159 0.96 KMT2A (0.66) KMT2AGAAHTTCA2CA5A
Ammonia Solution, Strong SCHEMBL9479957 0.96 KMT2A (0.70) KMT2AGAAHTTCA2CA5A
SCHEMBL10474225 0.96 KMT2A (0.70) KMT2AGAAHTTCA2CA5A
SCHEMBL4579511 0.96 KMT2A (0.70) KMT2AGAAHTTCA2CA5A
Water SCHEMBL8747065 0.96 KMT2A (0.70) KMT2AGAAHTTCA2CA5A

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
CN-109415312-A Alkylation 通用电气健康护理有限公司 2019-03-01 CN disclosed
CN-106456632-A Methods of inhibiting necroptosis 催化剂治疗私人有限公司 2017-02-22 CN disclosed
EP-0609025-B1 Process for producing optically active epoxy alcohol derivatives ARCO CHEM TECH (US) 1996-04-17 EP disclosed
US-5436370-A From nitrobenzene, chlorosulfonic acid, thionyl chloride HOECHST AG (DE) 1995-07-25 US disclosed
EP-0609025-A1 Process for producing optically active epoxy alcohol derivatives ARCO Chemical Technology, L.P. (US) 1994-08-03 EP disclosed
US-5252759-A Reacting with organic sulfonyl halide to produce organic sulfonate ARCO CHEMICAL TECHNOLOGY, L.P. (US) 1993-10-12 US disclosed
US-5086128-A HIGH MOLECULAR WEIGHT ARYLENE SULPHIDE POLYMER MELT MIXED WITH AROMATIC NITRO COMPOUND BAYER AKTIENGESELLSCHAFT (DE) 1992-02-04 US disclosed
WO-1991013863-A1 METHOD FOR PREPARING 3-NITROBENZENE SULPHONIC ACID CHLORIDE HOECHST AKTIENGESELLSCHAFT (DE) 1991-09-19 WO disclosed
US-4656290-A Process for preparing thio, dithio or carbonyl compounds CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA RT. (HU) 1987-04-07 US disclosed
US-4587275-A AROMATIC DIAMINE WITH SULFONIC ACID GROUP AS CHAIN EXTENSION AGENT BAYER AKTIENGESELLSCHAFT (DE) 1986-05-06 US disclosed
US-4388246-A THERMAL SPLITTING OF CARBAMATES BAYER AKTIENGESELLSCHAFT (DE) 1983-06-14 US disclosed
US-4368260-A Photographic light sensitive element KONISHIROKU PHOTO INDUSTRY CO., LTD. (JP) 1983-01-11 US disclosed
US-4195992-A AZO DYE AGFA-GEVAERT AKTIENGESELLSCHAFT (DE) 1980-04-01 US disclosed