Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1499337

Cc1ccc(S(=O)(=O)N[C@@H](CCCCN)C(=O)O)cc1.Cl.O=C(CCl)CCl

nearest known ligand 0.65

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
ITGB3 known ✓ P05106 1/20 0.52
ITGA2B known ✓ P08514 1/20 0.52
MMP13 known ✓ P45452 2/20 0.46
MMP8 known ✓ P22894 4/20 0.44
CA2 known ✓ P00918 1/20 0.43
MMP9 P14780 12/20 0.65
MMP2 P08253 11/20 0.65
TDP1 Q9NUW8 1/20 0.49
SLC1A3 P43003 1/20 0.46
SLC1A2 P43004 1/20 0.46
SLC1A1 P43005 1/20 0.46
MMP3 P08254 1/20 0.46
ADAMTS4 O75173 1/20 0.44
PLAU P00749 1/20 0.44
HPN P05981 1/20 0.44
MMP12 P39900 3/20 0.44
MMP14 P50281 3/20 0.44
CA1 P00915 1/20 0.43
ALDH1A1 P00352 1/20 0.43
TSHR P16473 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
Hydrochloric Acid SCHEMBL14059214 1.00 MMP9 (0.65) MMP9MMP2ITGB3ITGA2BTDP1
SCHEMBL2038720 0.99 MMP9 (0.67) MMP9MMP2ITGB3ITGA2BTDP1
SCHEMBL77677 0.99 MMP9 (0.67) MMP9MMP2ITGB3ITGA2BTDP1
Hydrochloric Acid SCHEMBL9087107 0.93 MMP9 (0.74) MMP9MMP2ITGB3ITGA2BTDP1
SCHEMBL8001084 0.92 MMP9 (0.76) MMP9MMP2ITGB3ITGA2BTDP1
SCHEMBL10585071 0.92 MMP9 (0.76) MMP9MMP2ITGB3ITGA2BTDP1
SCHEMBL457772 0.92 MMP9 (0.76) MMP9MMP2ITGB3ITGA2BTDP1
Hydrochloric Acid SCHEMBL14059216 0.91 MMP9 (0.68) MMP9MMP2ITGB3ITGA2BTDP1
Hydrochloric Acid SCHEMBL28895937 0.91 MMP9 (0.68) MMP9MMP2ITGB3ITGA2BTDP1
SCHEMBL8322406 0.91 MMP9 (0.71) MMP9MMP2ITGB3ITGA2BTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8268604-B2 Compositions for forming immobilized biological layers for sensing ABBOTT POINT OF CARE INC. (US) 2012-09-18 US claimed
JP-2011508221-A 2011-03-10 JP claimed
US-20100255120-A1 COMPOSITIONS FOR FORMING IMMOBILIZED BIOLOGICAL LAYERS FOR SENSING ABBOTT POINT OF CARE INC. 2010-10-07 US claimed
EP-2225388-A1 COMPOSITIONS FOR FORMING IMMOBIIZED BIOLOGICAL LAYERS FOR SENSING Abbott Point Of Care, Inc. (US) 2010-09-08 EP claimed
WO-2009082699-A1 COMPOSITIONS FOR FORMING IMMOBIIZED BIOLOGICAL LAYERS FOR SENSING I-STAT CORPORATION (US) 2009-07-02 WO claimed
EP-1549758-A4 FELINE PANCREATIC LIPASE COMPOSITION AND METHOD OF PREPARING AND USING SUCH COMPOSITION TEXAS A & M UNIV SYS (US) 2006-05-03 EP claimed
EP-1549758-A2 FELINE PANCREATIC LIPASE COMPOSITION AND METHOD OF PREPARING AND USING SUCH COMPOSITION Texas A & M University System (US) 2005-07-06 EP claimed
WO-2003093232-A2 FELINE PANCREATIC LIPASE COMPOSITION AND METHOD OF PREPARING AND USING SUCH COMPOSITION TEXAS A & M UNIVERSITY SYSTEM (US) 2003-11-13 WO claimed
US-20030207333-A1 Feline pancreatic lipase composition and method of preparing and using such composition TEXAS A&M UNIVERSITY SYSTEM, THE 2003-11-06 US claimed
EP-0066786-B1 METHOD OF PRODUCING A COLON SPECIFIC ANTIGEN P TRYPTIC PEPTIDE AND ANTI-COLON SPECIFIC ANTIGEN P ANTIBODIES Goldenberg, Milton David (US) 1986-05-14 EP claimed
US-4468457-A SPECIFIC ANTIBODIES FOR GASTROINTESTINAL TRACT Goldenberg, David M. (US) 1984-08-28 US claimed
US-12440833-B2 Sample containers adapted for acoustic ejections and sample preservation and methods thereof LABCYTE INC. (US) 2025-10-14 US disclosed
US-20210299093-A1 PROPHYLACTIC OR THERAPEUTIC AGENT FOR PULMONARY HYPERTENSION COMPRISING UNSATURATED 5-MEMBERED HETEROCYCLE-CONTAINING COMPOUND TOHOKU UNIVERSITY (JP) 2021-09-30 US disclosed
EP-2702388-B1 SAMPLE CONTAINERS ADAPTED FOR ACOUSTIC EJECTIONS AND SAMPLE PRESERVATION AND METHODS THEREOF LABCYTE INC (US) 2021-08-04 EP disclosed
EP-3822612-A1 METHOD FOR HOLDING A LIQUID SAMPLE IN A CONTAINER Labcyte Inc. (US) 2021-05-19 EP disclosed
US-7455998-B2 Methods for forming structurally defined organic molecules DOW CORNING CORPORATION (US) 2008-11-25 US disclosed
EP-1725669-A1 METHODS FOR FORMING STRUCTURALLY DEFINED ORGANIC MOLECULES Dow Corning Corporation (US) 2006-11-29 EP disclosed
WO-2005085459-A1 METHODS FOR FORMING STRUCTURALLY DEFINED ORGANIC MOLECULES DOW CORNING CORPORATION (US) 2005-09-15 WO disclosed
US-20050196849-A1 Methods for forming structurally defined organic molecules DOW CORNING CORPORATION 2005-09-08 US disclosed
US-4341697-A Antigenic material BURROUGHS WELLCOME CO. (US) 1982-07-27 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20210299093-A1 PROPHYLACTIC OR THERAPEUTIC AGENT FOR PULMONARY HYPERTENSION COMPRISING UNSATURATED 5-MEMBERED HETEROCYCLE-CONTAINING COMPOUND PTGIR, AGTR1, SHROOM3 ITGB3 3762/4885ITGA2B 4573/4885MMP13 3495/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.