Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2960053

C(CC=Nc1ccccc1)=Nc1ccccc1.Cl

nearest known ligand 0.43

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
MAOA known ✓ P21397 1/20 0.40
GLA known ✓ P06280 1/20 0.38
PTGS1 known ✓ P23219 1/20 0.35
PTGS2 known ✓ P35354 1/20 0.35
GAA known ✓ P10253 1/20 0.35
HTR3E known ✓ A5X5Y0 1/20 0.35
HTR3B known ✓ O95264 1/20 0.35
HTR3A known ✓ P46098 1/20 0.35
HTR3D known ✓ Q70Z44 1/20 0.35
HTR3C known ✓ Q8WXA8 1/20 0.35
CA2 known ✓ P00918 1/20 0.33
ALDH1A1 P00352 4/20 0.43
KDM4E B2RXH2 2/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
KMT2A Q03164 5/20 0.36
CYP2C9 P11712 1/20 0.36
MAPT P10636 4/20 0.35
NPC1 O15118 4/20 0.35
RAB9A P51151 4/20 0.35
MEN1 O00255 3/20 0.35

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 SCHEMBL2960051 1.00 ALDH1A1 (0.43) ALDH1A1MAOAKDM4EGLAL3MBTL1
SCHEMBL7516473 0.97 ALDH1A1 (0.45) ALDH1A1MAOAKDM4EGLAL3MBTL1
SCHEMBL10090559 0.97 ALDH1A1 (0.45) ALDH1A1MAOAKDM4EGLAL3MBTL1
Hydrochloric Acid SCHEMBL8488644 0.85 ALDH1A1 (0.36) ALDH1A1MAOAKDM4EGLAL3MBTL1
SCHEMBL16187277 0.85 ALDH1A1 (0.37) ALDH1A1MAOAKDM4EGLAL3MBTL1
SCHEMBL10122037 0.82 ALDH1A1 (0.38) ALDH1A1MAOAKDM4EGLAL3MBTL1
SCHEMBL15910559 0.82 ALDH1A1 (0.38) ALDH1A1MAOAKDM4EGLAL3MBTL1
SCHEMBL3803101 0.82 ALDH1A1 (0.38) ALDH1A1MAOAKDM4EGLAL3MBTL1
SCHEMBL19932533 0.82 ALDH1A1 (0.38) ALDH1A1MAOAKDM4EGLAL3MBTL1
SCHEMBL3803095 0.82 ALDH1A1 (0.38) ALDH1A1MAOAKDM4EGLAL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118908921-A Anionic pentamethine cyanine and preparation method and application thereof 华中科技大学 2024-11-08 CN disclosed
CN-114805310-B Fluorescent compounds containing hydroxy-substituted triazines and methods of making the same 佰爱特有限公司 2024-07-26 CN disclosed
US-11981955-B2 Polymethine compounds and their use as fluorescent labels ILLUMINA CAMBRIDGE LIMITED (GB) 2024-05-14 US disclosed
EP-3831825-B1 POLYMETHINE COMPOUNDS AND THEIR USE AS FLUORESCENT LABELS ILLUMINA CAMBRIDGE LTD (GB) 2023-09-06 EP disclosed
US-11707537-B2 Conformational restriction of cyanine fluorophores in far-red and near-IR range THE USA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2023-07-25 US disclosed
US-20230167486-A1 POLYMETHINE COMPOUNDS AND THEIR USE AS FLUORESCENT LABELS ILLUMINA CAMBRIDGE LIMITED (GB) 2023-06-01 US disclosed
US-11530439-B2 Polymethine compounds and their use as fluorescent labels ILLUMINA CAMBRIDGE LIMITED (GB) 2022-12-20 US disclosed
EP-4058190-A1 COMPOSITIONS AND METHODS FOR CONTROLLED DELIVERY AND PROTECTION OF THERAPEUTIC AGENTS Board of Regents, The University of Texas System (US) 2022-09-21 EP disclosed
US-20210198724-A1 POLYMETHINE COMPOUNDS AND THEIR USE AS FLUORESCENT LABELS ILLUMINA CAMBRIDGE LIMITED (GB) 2021-07-01 US disclosed
EP-3831825-A1 POLYMETHINE COMPOUNDS AND THEIR USE AS FLUORESCENT LABELS Illumina Cambridge Limited (GB) 2021-06-09 EP disclosed
US-20090017441-A1 Reacting unsubstituted or substituted 2-methylbenzothiazole, 2-methylbenzooxazole or 2,3,3-trimethyl-3H-indoline with substituted or unsubstituted benzylhalide, forming 4-methylquinoline quaternary ammonium salt intermediates, condensing with N,N'-diphenylformamidine; for staining nucleic acids SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (CN) 2009-01-15 US disclosed
WO-2008127768-A1 A CYANINE-BASED PROBE\\TAG-PEPTIDE PAIR FOR FLUORESCENCE PROTEIN IMAGING AND FLUORESCENCE PROTEIN IMAGING METHODS BATTELLE MEMORIAL INSTITUTE (US) 2008-10-23 WO disclosed
US-20080254546-A1 A Cyanine-based probe\\tag-peptide pair for fluorescence protein imaging and fluorescence protein imaging methods BATTELLE MEMORIAL INSTITUTE 2008-10-16 US disclosed
EP-1196398-A4 BRIDGED FLUORESCENT DYES, THEIR PREPARATION AND THEIR USE IN ASSAYS SURROMED INC (US) 2002-11-06 EP disclosed
US-6403807-B1 CYANINE DYES HAVING SEPARATE SECOND LINKING CHAIN JOINING TWO HETEROCYCLES TO RESTRAIN COMPOUND INTO DESIRED CONFORMATION WHICH ABSORBS ELECTROMAGNETIC ENERGY AND EMITS FLUORESCENCE AT SPECIFIED WAVELENGTHS SURROMED, INC. 2002-06-11 US disclosed
EP-1196398-A1 BRIDGED FLUORESCENT DYES, THEIR PREPARATION AND THEIR USE IN ASSAYS Surromed, Inc. (US) 2002-04-17 EP disclosed
WO-2001002374-A1 BRIDGED FLUORESCENT DYES, THEIR PREPARATION AND THEIR USE IN ASSAYS SURROMED, INC. (US) 2001-01-11 WO disclosed
EP-0241696-B1 NAPHTHOLACTAM DYES AND OPTICAL RECORDING CARRIER CONTAINING THEM BASF Aktiengesellschaft (DE) 1993-07-14 EP disclosed
US-4939012-A Semiconductor laser sensitive BASF AKTIENGESELLSCHAFT (DE) 1990-07-03 US disclosed
US-4876356-A LASER SENSITIVE BASF AKTIENGESELLSCHAFT (DE) 1989-10-24 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 (7 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-11981955-B2 Polymethine compounds and their use as fluorescent labels POLRMT, FBL, POLM MAOA 1580/4885GLA 2390/4885PTGS1 3106/4885
US-20210198724-A1 POLYMETHINE COMPOUNDS AND THEIR USE AS FLUORESCENT LABELS POLRMT, FBL, POLM MAOA 1580/4885GLA 2390/4885PTGS1 3106/4885
US-20230167486-A1 POLYMETHINE COMPOUNDS AND THEIR USE AS FLUORESCENT LABELS POLRMT, FBL, POLM MAOA 1580/4885GLA 2390/4885PTGS1 3106/4885
US-11530439-B2 Polymethine compounds and their use as fluorescent labels POLRMT, FBL, POLM MAOA 1580/4885GLA 2390/4885PTGS1 3106/4885
US-20090017441-A1 Reacting unsubstituted or substituted 2-methylbenzothiazole, 2-methylbenzooxazole or 2,3,3-trimethyl-3H-indoline with substituted or unsubstituted benzylhalide, forming 4-methylquinoline quaternary ammonium salt intermediates, condensing with N,N'-diphenylformamidine; for staining nucleic acids RCC1, DNMT3A, H1-4 MAOA 3409/4885GLA 4002/4885PTGS1 4639/4885
US-20080254546-A1 A Cyanine-based probe\\tag-peptide pair for fluorescence protein imaging and fluorescence protein imaging methods AS3MT, EBPL, GLI2 MAOA 4307/4885GLA 679/4885PTGS1 4808/4885
US-11707537-B2 Conformational restriction of cyanine fluorophores in far-red and near-IR range IK, FAR1, SPR MAOA 3261/4885GLA 723/4885PTGS1 4592/4885

“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.