Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4253880

CC1=C(C)N(Cc2ccccc2)C(C)N1Cc1ccccc1.Cl

nearest known ligand 0.46

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 16)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.44
CHRM2 known ✓ P08172 1/20 0.40
CHRM4 known ✓ P08173 1/20 0.40
CHRM5 known ✓ P08912 1/20 0.40
SIGMAR1 known ✓ Q99720 1/20 0.40
EHMT2 Q96KQ7 1/20 0.46
LMNA P02545 3/20 0.41
POLB P06746 1/20 0.41
SMO Q99835 2/20 0.41
MEN1 O00255 2/20 0.41
KMT2A Q03164 2/20 0.41
BRD4 O60885 1/20 0.41
ALOX12 P18054 1/20 0.40
MAPK1 P28482 1/20 0.40
ALDH1A1 P00352 1/20 0.39
NPSR1 Q6W5P4 1/20 0.39

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
SCHEMBL4076507 0.98 EHMT2 (0.47) EHMT2ACHELMNAPOLBSMO
Hydrochloric Acid SCHEMBL28802075 0.83 SIGMAR1 (0.58) LMNAMEN1KMT2ACHRM5SIGMAR1
SCHEMBL18844475 0.81 BRD4 (0.53) EHMT2ACHELMNASMOBRD4
SCHEMBL28330649 0.78 EHMT2 (0.44) EHMT2ACHELMNASMOMEN1
SCHEMBL13889204 0.73 CHRM2 (0.50) EHMT2ACHELMNAPOLBMEN1
Hydrochloric Acid SCHEMBL18789343 0.72 ACHE (0.46) EHMT2ACHELMNAPOLBMEN1
Hydrochloric Acid SCHEMBL11780582 0.71 ACHE (0.53) ACHELMNAPOLBSIGMAR1
SCHEMBL13317117 0.70 ACHE (0.44) EHMT2ACHELMNAPOLBMEN1
SCHEMBL15202275 0.70 ACHE (0.47) EHMT2ACHELMNAPOLBMEN1
SCHEMBL1078734 0.70 ACHE (0.47) EHMT2ACHELMNAPOLBMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1536787-A4 IMIDAZOLE ALKALOIDS FROM LEPIDIUM MEYENII AND METHODS OF USAGE PURE WORLD BOTAN INC (US) 2009-02-25 EP disclosed
CN-1684680-A Imidazole alkaloid of lepidium meyenii and application thereof PURE WORLD BOTAN INC (US) 2005-10-19 CN disclosed
US-20050171081-A1 Imidazole alkaloids from lepidium meyenii and methods of usage PURE WORLD BOTANICALS, INC. (US) 2005-08-04 US disclosed
US-20050171081-A1 Imidazole alkaloids from lepidium meyenii and methods of usage PURE WORLD BOTANICALS, INC. (US) 2005-08-04 US disclosed
EP-1536787-A2 IMIDAZOLE ALKALOIDS FROM LEPIDIUM MEYENII AND METHODS OF USAGE Pure World Botanicals, Inc. (US) 2005-06-08 EP disclosed
US-6878731-B2 Imidazole alkaloids from Lepidium meyenii and methods of usage PURE WORLD BOTANICALS, INC. (US) 2005-04-12 US disclosed
US-6878731-B2 Imidazole alkaloids from Lepidium meyenii and methods of usage PURE WORLD BOTANICALS, INC. (US) 2005-04-12 US disclosed
WO-2004016216-A2 IMIDAZOLE ALKALOIDS FROM LEPIDIUM MEYENII AND METHODS OF USAGE PURE WORLD BOTANICALS, INC. (US) 2004-02-26 WO disclosed
US-20040034079-A1 Imidazole alkaloids from lepidium meyenii and methods of usage Naturex, S.A. (FR) 2004-02-19 US disclosed
US-20040034079-A1 Imidazole alkaloids from lepidium meyenii and methods of usage Naturex, S.A. (FR) 2004-02-19 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 (2 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-20040034079-A1 Imidazole alkaloids from lepidium meyenii and methods of usage MELK, MAGI3, INMT ACHE 849/4885CHRM2 1004/4885CHRM4 717/4885
US-20050171081-A1 Imidazole alkaloids from lepidium meyenii and methods of usage MELK, MAGI3, INMT ACHE 745/4885CHRM2 1013/4885CHRM4 718/4885

“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.