Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4734485

CNCC(=O)c1cccc(O)c1.Cl

nearest known ligand 0.53

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
CA2 known ✓ P00918 1/20 0.50
PARP1 known ✓ P09874 1/20 0.48
GAA known ✓ P10253 3/20 0.46
ADRB2 known ✓ P07550 1/20 0.41
ADRB1 known ✓ P08588 1/20 0.41
HTR1A known ✓ P08908 1/20 0.41
ADRA2A known ✓ P08913 1/20 0.41
ADRB3 known ✓ P13945 1/20 0.41
ADRA2B known ✓ P18089 1/20 0.41
ADRA2C known ✓ P18825 1/20 0.41
DRD1 known ✓ P21728 1/20 0.41
HTR7 known ✓ P34969 1/20 0.41
ADRA1A known ✓ P35348 1/20 0.41
ADRA1B known ✓ P35368 1/20 0.41
DRD3 known ✓ P35462 1/20 0.41
SLC6A3 known ✓ Q01959 1/20 0.41
ESR1 known ✓ P03372 1/20 0.41
ESR2 known ✓ Q92731 1/20 0.41
KDM4E B2RXH2 4/20 0.53
ALDH1A1 P00352 2/20 0.53

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 SCHEMBL31491126 1.00 KDM4E (0.53) KDM4EALDH1A1EGLN2CA12CA1
SCHEMBL29757148 0.98 KDM4E (0.55) KDM4EALDH1A1EGLN2CA12CA1
SCHEMBL1274658 0.98 KDM4E (0.55) KDM4EALDH1A1EGLN2CA12CA1
Sulfuric Acid SCHEMBL4016436 0.92 KDM4E (0.49) KDM4EALDH1A1EGLN2CA12CA1
Hydrochloric Acid SCHEMBL11756049 0.83 KDM4E (0.50) KDM4EALDH1A1EGLN2CA12CA1
Hydrochloric Acid SCHEMBL15973303 0.81 CES2 (0.53) KDM4EALDH1A1PARP1MAPTCTNNB1
SCHEMBL7446526 0.81 KDM4E (0.51) KDM4EALDH1A1EGLN2CA12CA1
SCHEMBL24229642 0.80 HDAC8 (0.55) KDM4EPARP1MAPTCTNNB1LMNA
Hydrochloric Acid SCHEMBL259354 0.79 KMT2A (0.60) KDM4EALDH1A1GAAMAPTHIF1A
SCHEMBL10481543 0.79 ERCC5 (0.60) KDM4EALDH1A1PARP1MAPTLMNA

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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101921197-A Preparation method of phenylephrine WEIFANG HAPPY PHARMACEUTICAL LTD 2010-12-22 CN claimed
US-20250312270-A1 READY-TO-INFUSE PHENYLEPHRINE COMPOSITIONS AMNEAL EU, LIMITED (IE) 2025-10-09 US disclosed
WO-2025059259-A1 NEW PROCESS FOR PHENYLEPHRINE AND SALBUTAMOL AND RELATED COMPOUNDS VIA ASYMETRIC TRANSFER HYDROGENATION OF UNPROTECTED AMINO KETONES VIRGINIA COMMONWEALTH UNIVERSITY (US) 2025-03-20 WO disclosed
US-20250025409-A1 READY-TO-INFUSE PHENYLEPHRINE COMPOSITIONS AMNEAL EU, LIMITED (IE) 2025-01-23 US disclosed
US-20210228507-A1 Phenylephrine Hydrochloride Compositions and Containers NEVAKAR INC. (US) 2021-07-29 US disclosed
CN-102234237-B Method for preparing L-phenylephrine hydrochloride CHIFENG ARKER PHARMACEUTICAL TECHNOLOGY CO LTD 2014-03-26 CN disclosed
CN-102234237-A Method for preparing L-phenylephrine hydrochloride CHIFENG ARKER PHARMACEUTICAL TECHNOLOGY CO LTD 2011-11-09 CN disclosed
CN-201791519-U Deoxidation adrenergic hydrogenation device WEIFANG HAPPY PHARMACEUTICAL CO LTD 2011-04-13 CN disclosed
CN-101921197-A Preparation method of phenylephrine WEIFANG HAPPY PHARMACEUTICAL LTD 2010-12-22 CN disclosed
WO-2008095678-A1 PROCESS FOR THE PREPARATION OF OPTICALLY ACTIVE 2-AMINO-1-PHENYLETHANOLS LONZA AG (CH) 2008-08-14 WO disclosed
WO-2008077560-A1 PROCESS FOR THE PREPARATION OF OPTICALLY ACTIVE 2-AMINO-1-PHENYLETHANOLS LONZA AG (CH) 2008-07-03 WO 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 (3 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-20250312270-A1 READY-TO-INFUSE PHENYLEPHRINE COMPOSITIONS REN, PEF1, AVPR2 CA2 1767/4885PARP1 4581/4885GAA 3612/4885
US-20250025409-A1 READY-TO-INFUSE PHENYLEPHRINE COMPOSITIONS REN, PEF1, AVPR2 CA2 1767/4885PARP1 4581/4885GAA 3612/4885
US-20210228507-A1 Phenylephrine Hydrochloride Compositions and Containers ADRA1A, ADRA2C, ADRB1 CA2 1277/4885PARP1 1804/4885GAA 1789/4885

“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.