Hydrochloric Acid

Hydrochloric Acid

SCHEMBL986711

CCN(CCCN(C)C)C(=O)S.Cl

nearest known ligand 0.39

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 15)

geneUniProtsupporting neighboursconfidence
PTGS1 known ✓ P23219 1/20 0.34
CA12 O43570 2/20 0.39
CA1 P00915 2/20 0.39
CA9 Q16790 2/20 0.39
DNM1 Q05193 4/20 0.38
LMNA P02545 2/20 0.37
USP2 O75604 1/20 0.35
ALDH1A1 P00352 1/20 0.35
TSHR P16473 1/20 0.35
ABCB11 O95342 1/20 0.34
CYP2E1 P05181 1/20 0.34
HTT P42858 1/20 0.34
GSDMD P57764 1/20 0.34
KDM4A O75164 7/20 0.34
KDM4C Q9H3R0 7/20 0.34

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
SCHEMBL6062643 0.98 CA12 (0.41) CA12CA1CA9DNM1LMNA
SCHEMBL1829140 0.80 CA12 (0.59) CA12CA1CA9LMNAALDH1A1
Hydrochloric Acid SCHEMBL27811822 0.79 CA12 (0.39) CA12CA1CA9DNM1LMNA
SCHEMBL13185664 0.78 LMNA (0.47) CA12CA1CA9DNM1LMNA
SCHEMBL1531387 0.77 CA12 (0.41) CA12CA1CA9DNM1LMNA
SCHEMBL6195760 0.75
SCHEMBL689389 0.74
Iodomethane SCHEMBL7516696 0.73 CA12 (0.38) CA12CA1CA9DNM1LMNA
Hydrochloric Acid SCHEMBL29191724 0.73 KDM4A (0.42) DNM1LMNAUSP2ALDH1A1TSHR
Hydrochloric Acid SCHEMBL986713 0.72 CA12 (0.41) CA12CA1CA9DNM1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250113829-A1 HIGH MOLECULAR WEIGHT MODIFIED RNA COMPOSITIONS nanoSUR LLC 2025-04-10 US disclosed
EP-4396348-A2 HIGH MOLECULAR WEIGHT MODIFIED DSRNA COMPOSITIONS Nanosur LLC (US) 2024-07-10 EP disclosed
WO-2023034849-A2 HIGH MOLECULAR WEIGHT MODIFIED dsRNA COMPOSITIONS nanoSUR LLC (US) 2023-03-09 WO disclosed
US-11174480-B2 Post-transcriptionally chemically modified double strand RNAs nanoSUR LLC (US) 2021-11-16 US disclosed
US-10988611-B2 Crosslinked polyvinylpyrrolidone compositions ISP INVESTMENTS LLC (US) 2021-04-27 US disclosed
US-10640769-B2 Post-transcriptionally chemically modified double strand RNAs nanoSUR LLC (US) 2020-05-05 US disclosed
US-20200060273-A1 FUNGICIDAL COMPOSITIONS NOVUS INTERNATIONAL, INC. 2020-02-27 US disclosed
US-10426077-B2 Seed flow lubricant compositions and uses thereof 3 Star Ag LLC (US) 2019-10-01 US disclosed
EP-3535274-A2 POST-TRANSCRIPTIONALLY CHEMICALLY MODIFIED DOUBLE STRAND RNAS Nanosur LLC (US) 2019-09-11 EP disclosed
EP-2358768-B1 CROSSLINKED POLYVINYLPYRROLIDONE COMPOSITIONS ISP INVESTMENTS LLC (US) 2019-07-03 EP disclosed
US-5550115-A BLEND OF BIOLOGICALLY ACTIVE MATERIAL AND SOLID PHASE SURFACTANT; TREATMENT OF AGRICULTURAL SUBSTRATES HENKEL CORPORATION (US) 1996-08-27 US disclosed
WO-1996016540-A1 BIOLOGICALLY ACTIVE COMPOSITION HENKEL CORPORATION (US) 1996-06-06 WO disclosed
EP-0508667-B1 Aqueous agricultural compositions, methods of making them and their use MONSANTO CO (US) 1996-06-05 EP disclosed
EP-0508667-A1 Aqueous agricultural compositions, methods of making them and their use MONSANTO COMPANY (US) 1992-10-14 EP disclosed
US-5118444-A Mixture of herbicide and amine-oxide surfactant WITCO CORPORATION (US) 1992-06-02 US disclosed
US-H303-H GLYCOSIDE-CONTAINING AGRICULTURAL TREATMENT COMPOSITION A. E. STALEY MANUFACTURING COMPANY (US) 1987-07-07 US disclosed
US-H224-H Glycoside-containing agricultural treatment composition A. E. STALEY MANUFACTURING COMPANY (US) 1987-03-03 US disclosed
US-4512989-A IMIDOESTERS OR IMIDOTHIOESTERS HOKKO CHEMICAL INDUSTRY CO., LTD. (JP) 1985-04-23 US disclosed
US-4420486-A Benzoxazolone derivatives, processes for preparation thereof and compositions containing them HOKKO CHEMICAL INDUSTRY CO., LTD. (JP) 1983-12-13 US disclosed
US-4391804-A Imidazole derivatives and fungicidal composition containing the same HOKKO CHEMICAL INDUSTRY COMPANY, LTD. (JP) 1983-07-05 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 (4 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-20250113829-A1 HIGH MOLECULAR WEIGHT MODIFIED RNA COMPOSITIONS NSUN2, NSUN3, RNGTT PTGS1 2858/4885CA12 4546/4885CA1 4858/4885
US-11174480-B2 Post-transcriptionally chemically modified double strand RNAs NSUN2, NSUN3, RNGTT PTGS1 2755/4885CA12 4395/4885CA1 4588/4885
US-20200060273-A1 FUNGICIDAL COMPOSITIONS ERG28, CYP51A1, CYP19A1 PTGS1 4396/4885CA12 1204/4885CA1 1205/4885
US-10640769-B2 Post-transcriptionally chemically modified double strand RNAs NSUN2, NSUN3, RNGTT PTGS1 2755/4885CA12 4395/4885CA1 4588/4885

“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.