Hydrochloric Acid

Hydrochloric Acid

SCHEMBL56953

CC(C)(C)NN.Cl

nearest known ligand 0.00

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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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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 SCHEMBL28422264 1.00 MAPT (0.32)
Hydrochloric Acid SCHEMBL22836521 1.00
Bromide SCHEMBL29012438 0.90
SCHEMBL9712415 0.90
Water SCHEMBL2134234 0.90
Hydrochloric Acid SCHEMBL696443 0.86
Oxalic Acid SCHEMBL1233371 0.79 ALOX15 (0.39)
SCHEMBL7123839 0.76
Acetone SCHEMBL19837822 0.76 LMNA (0.43)
Acetic Acid SCHEMBL7438398 0.73 FFAR3 (0.47)

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 1473 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120136791-A Pyridaben intermediate II New synthesis process of chloropyridazinone 河北优农派生物科技有限公司 2025-06-13 CN claimed
CN-116425725-B Preparation method and application of myocardial perfusion imaging agent precursor 北京先通国际医药科技股份有限公司 2025-05-06 CN claimed
CN-116715656-B Preparation method and application of myocardial perfusion imaging agent precursor 北京先通国际医药科技股份有限公司 2025-05-02 CN claimed
CN-118930454-A Bisamide compound containing hydrazide structure and synthetic method and application thereof 河北威远生物化工有限公司 2024-11-12 CN claimed
CN-118724772-A Preparation method of dihydroxyethyl bisphenol S 广东优巨先进新材料股份有限公司 2024-10-01 CN claimed
CN-116715656-A Preparation method and application of myocardial perfusion imaging agent precursor 北京先通国际医药科技股份有限公司 2023-09-08 CN claimed
CN-116425725-A Preparation method and application of myocardial perfusion imaging agent precursor 北京先通国际医药科技股份有限公司 2023-07-14 CN claimed
CN-114031556-B Synthetic method for preparing 5-amino-N-aryl-3-arylpyrazole compound by green one-pot method 温州大学 2023-03-31 CN claimed
CN-115141183-B Preparation method and application of myocardial perfusion developer precursor 北京先通国际医药科技股份有限公司 2023-03-21 CN claimed
CN-113248351-B Preparation method of 6-chloro-2-methoxytoluene and synthetic process of methoxyfenozide 绍兴上虞新银邦生化有限公司 2022-10-11 CN claimed
EP-0639559-A1 Preparation of 1,2-diacyl-2-(t-alkyl)hydrazines ROHM AND HAAS COMPANY (US) 1995-02-22 EP claimed
US-4692269-A BLOWING AGENTS; CLOSED-CELL FOAMS PENNWALT CORPORATION (US) 1987-09-08 US claimed
EP-0220751-A2 Foamable and cross-linkable unsaturated polyester composition PENNWALT CORPORATION (US) 1987-05-06 EP claimed
EP-0220364-A2 Reaction of certain hydrazide compounds with free radical initiators to produce crosslinked polymer foams PENNWALT CORPORATION (US) 1987-05-06 EP claimed
EP-0219595-A2 A gas-realising composition for tailoring gas evolution of system PENNWALT CORPORATION (US) 1987-04-29 EP claimed
EP-0216990-A2 Foaming and vulcanizing of elastomeric polymers PENNWALT CORPORATION (US) 1987-04-08 EP claimed
US-4636528-A Foaming of unsaturated polyester resin at elevated temperatures PENNWALT CORPORATION (US) 1987-01-13 US claimed
US-4607060-A FREE RADICAL CATALYSIS PENNWALT CORPORATION (US) 1986-08-19 US claimed
US-4588752-A CLOSED-CELL, TERT-ALKYLHYDRAZINIUM SALT OR HYDRAZIDE FOAMING AGENT PENNWALT CORPORATION (US) 1986-05-13 US claimed
US-4008273-A AZO INTERMEDIATE PENNWALT CORPORATION (US) 1977-02-15 US claimed