Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2327786

CC(=O)Oc1ccncc1.Cl

nearest known ligand 0.56

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
HSP90AA1 known ✓ P07900 1/20 0.46
GAA known ✓ P10253 1/20 0.46
ESR1 known ✓ P03372 2/20 0.45
SLC6A3 known ✓ Q01959 2/20 0.45
ADRA2A known ✓ P08913 1/20 0.45
PDE4A known ✓ P27815 1/20 0.45
ADRA1A known ✓ P35348 1/20 0.45
OPRK1 known ✓ P41145 1/20 0.45
TTR known ✓ P02766 1/20 0.44
GLA known ✓ P06280 1/20 0.43
CYP19A1 known ✓ P11511 1/20 0.43
CHRM2 known ✓ P08172 1/20 0.42
CHRM1 known ✓ P11229 1/20 0.42
SLC6A2 known ✓ P23975 1/20 0.42
LMNA P02545 5/20 0.56
HSD17B10 Q99714 3/20 0.52
MAPT P10636 3/20 0.50
POLB P06746 1/20 0.50
PKM P14618 1/20 0.50
CYP2C9 P11712 2/20 0.48

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 SCHEMBL27539616 1.00 LMNA (0.56) LMNAHSD17B10MAPTPOLBPKM
SCHEMBL701147 0.98 LMNA (0.58) LMNAHSD17B10MAPTPOLBPKM
SCHEMBL380364 0.81 HSD17B10 (0.56) LMNAHSD17B10MAPTCYP2C9SMN1; SMN2
SCHEMBL7781973 0.80 HSD17B10 (0.50) LMNAHSD17B10MAPTPOLBCYP2C9
SCHEMBL269329 0.80 LMNA (0.80) LMNAHSD17B10MAPTPOLBPKM
SCHEMBL2625475 0.78 ELANE (0.60) LMNAHSD17B10CYP2C9SMN1; SMN2CYP1A2
SCHEMBL18727667 0.78 HSD17B10 (0.58) LMNAHSD17B10CYP2C9SMN1; SMN2CYP1A2
Lithium SCHEMBL30522746 0.78 LMNA (0.76) LMNAHSD17B10MAPTPOLBPKM
SCHEMBL14760365 0.78 LMNA (0.76) LMNAHSD17B10MAPTPOLBPKM
Hydrochloric Acid SCHEMBL10772752 0.77 HSD17B10 (0.52) LMNAHSD17B10MAPTCYP2C9SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4582423-A1 NOVEL TRICYCLIC DERIVATIVE COMPOUND AND USES THEREOF Hanmi Pharm. Co., Ltd. (KR) 2025-07-09 EP disclosed
WO-2024080788-A1 NOVEL TRICYCLIC DERIVATIVE COMPOUND AND USES THEREOF 한미약품 주식회사 2024-04-18 WO disclosed
CN-116059390-A Prodrugs of cytotoxic actives with enzymatically cleavable groups 拜耳制药股份公司 2023-05-05 CN disclosed
CN-110312533-A Prodrugs of cytotoxic active agents having an enzymatically cleavable group 拜耳公司 2019-10-08 CN disclosed
EP-3432934-A1 PRODRUGS OF CYTOTOXIC ACTIVE AGENTS HAVING ENZYMATICALLY CLEAVABLE GROUPS Bayer Pharma Aktiengesellschaft (DE) 2019-01-30 EP disclosed
CN-108883195-A Prodrugs of cytotoxic active substances with enzymatically cleavable groups 拜耳制药股份公司 2018-11-23 CN disclosed
CN-104428293-B Adjust the benzimidazole of TNF α UCB生物制药私人有限公司 2018-06-08 CN disclosed
CN-107921288-A The targeting conjugate of KSP inhibitor 拜耳医药股份有限公司 2018-04-17 CN disclosed
CN-104428293-A TNF -alpha modulating benzimidazoles UCB PHARMA SA 2015-03-18 CN disclosed
US-8530650-B2 2, 5-diamino-substituted pyrido [4, 3-D] pyrimidines as autotaxin inhibitors against cancer MERCK PATENT GMBH (DE) 2013-09-10 US disclosed
CN-1020104-C Process for preparing 3-propenyl cephem derivatives EISAI CO LTD (JP) 1993-03-17 CN disclosed
US-5089491-A Active against both gram-negative and gram-positive bacteria EISAI CO., LTD. (JP) 1992-02-18 US disclosed
EP-0264091-B1 3-PROPENYLCEPHEM DERIVATIVE, PREPARATION THEREOF, CHEMICAL INTERMEDIATES THEREIN, PHARMACEUTICAL COMPOSITION AND USE Eisai Co., Ltd. (JP) 1992-02-05 EP disclosed
US-5066812-A Chemical intermediates for bactericides EISAI CO., LTD. (JP) 1991-11-19 US disclosed
US-5006649-A Bactericides EISAI, CO. (JP) 1991-04-09 US disclosed
US-4921850-A GRAMNEGATIVE AND GRAMPOSITIVE BACTERICIDE EISAI CO., LTD. (JP) 1990-05-01 US disclosed
US-4797411-A ANTITUMOR AGENTS FARMITALIA CARLO ERBA S.P.A. (IT) 1989-01-10 US disclosed
CN-87107610-A Process for the preparation of cephem derivatives and intermediates therefor 1988-06-01 CN disclosed
EP-0264091-A2 3-Propenylcephem derivative, preparation thereof, chemical intermediates therein, pharmaceutical composition and use Eisai Co., Ltd. (JP) 1988-04-20 EP disclosed
EP-0253681-A2 Cycloalkyl-substituted 4-pyridyl derivatives and process for their preparation FARMITALIA CARLO ERBA S.r.l. (IT) 1988-01-20 EP disclosed