Hydrochloric Acid

Hydrochloric Acid

SCHEMBL742748

CC(C)(C)c1cc(NC(=O)Nc2ccc(-c3cn4c(n3)sc3ccc(OCCN5CCOCC5)cc34)cc2)no1.Cl.Cl

nearest known ligand 0.99

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
▸ FLT3 known ✓ P36888 20/20 0.99
▸ KDR known ✓ P35968 2/20 0.91
▸ ABL1 known ✓ P00519 1/20 0.90
▸ NTRK1 known ✓ P04629 1/20 0.90
▸ LCK known ✓ P06239 1/20 0.90
▸ CSF1R known ✓ P07333 1/20 0.90
▸ RET known ✓ P07949 1/20 0.90
▸ PDGFRB known ✓ P09619 1/20 0.90
▸ KIT known ✓ P10721 1/20 0.90
▸ PDGFRA known ✓ P16234 1/20 0.90
▸ FLT1 known ✓ P17948 1/20 0.90
▸ FLT4 known ✓ P35916 1/20 0.90
▸ ITK known ✓ Q08881 1/20 0.90
▸ NTRK3 known ✓ Q16288 1/20 0.90
▸ MAPK14 known ✓ Q16539 1/20 0.90
▸ NTRK2 known ✓ Q16620 1/20 0.90
▸ BMPR1B O00238 1/20 0.90
▸ MUSK O15146 1/20 0.90
▸ EPHB6 O15197 1/20 0.90
▸ MAP3K7 O43318 1/20 0.90

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 SCHEMBL74122 1.00 FLT3 (0.99) FLT3KDRBMPR1BMUSKEPHB6
SCHEMBL72924 0.99 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL29435035 0.95 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL74121 0.95 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL742377 0.95 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL72923 0.94 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
Quizartinib SCHEMBL29349937 0.94 FLT3 (1.00) FLT3KDRBMPR1BMUSKEPHB6
SCHEMBL1759300 0.93 FLT3 (0.87) FLT3KDRBMPR1BMUSKEPHB6
SCHEMBL1759073 0.93 FLT3 (0.87) FLT3KDRBMPR1BMUSKEPHB6
Hydrochloric Acid SCHEMBL75153 0.92 FLT3 (0.84) FLT3KDRBMPR1BMUSKEPHB6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3260119-B1 COMBINATION METHOD FOR TREATING CANCER DAIICHI SANKYO CO LTD (JP) 2023-11-15 — — EP claimed
US-10716790-B2 Method for treating cancer by combined use DAIICHI SANKYO COMPANY, LIMITED (JP) 2020-07-21 — — US claimed
EP-2521782-B1 FLT3 RECEPTOR ANTAGONISTS FOR THE TREATMENT OR THE PREVENTION OF PAIN DISORDERS INST NAT SANTE RECH MED (FR) 2019-04-10 — — EP claimed
EP-2903593-B1 TABLET CONTAINING COMPOSITE WITH CYCLODEXTRIN AMBIT BIOSCIENCES CORP (US) 2018-03-21 — — EP claimed
EP-3260119-A1 COMBINATION METHOD FOR TREATING CANCER DAIICHI SANKYO COMPANY, LIMITED (JP) 2017-12-27 — — EP claimed
US-20170216302-A1 METHOD FOR TREATING CANCER BY COMBINED USE DAIICHI SANKYO COMPANY, LIMITED (JP) 2017-08-03 — — US claimed
US-9675549-B2 Tablet containing composite with cyclodextrin AMBIT BIOSCIENCES CORPORATION (US) 2017-06-13 — — US claimed
US-20150250720-A1 TABLET CONTAINING COMPOSITE WITH CYCLODEXTRIN DAIICHI SANKYO COMPANY, LIMITED (JP) 2015-09-10 — — US claimed
US-9109227-B2 FLT3 receptor antagonists for the treatment or the prevention of pain disorders INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) (FR) 2015-08-18 — — US claimed
US-20260048099-A1 SYNERGISTIC INTERACTIONS FOR IMPROVED CANCER TREATMENT THE US SECRETARY DEPARMENT OF HEALTH AND HUMAN SERVICE (US) 2026-02-19 — — US disclosed
EP-3260119-B1 COMBINATION METHOD FOR TREATING CANCER DAIICHI SANKYO CO LTD (JP) 2023-11-15 — — EP disclosed
EP-3668867-B1 SYNTHESIS, PHARMACOLOGY AND USE OF NEW AND SELECTIVE FMS-LIKE TYROSINE KINASE 3 (FLT3) FLT3 INHIBITORS UNIV REGENSBURG (DE) 2023-10-04 — — EP disclosed
US-11384076-B2 Synthesis, pharmacology and use of new and selective FMS-like tyrosine kinase 3 (FLT3) FLT3 inhibitors UNIVERSITÄT REGENSBURG (DE) 2022-07-12 — — US disclosed
EP-3898626-A1 SUBSTITUTED PYRAZOLO[1,5-A]PYRIDINE COMPOUNDS AS INHIBITORS OF FGFR TYROSINE KINASES Array Biopharma, Inc. (US) 2021-10-27 — — EP disclosed
US-20130005966-A1 PROCESS FOR THE PREPARATION OF IMIDAZO[2,1-B][1,3]BENZOTHIAZOLE DERIVATIVES AMBIT BIOSCIENCES CORP. (US) 2013-01-03 — — US disclosed
EP-2521782-A1 FLT3 RECEPTOR ANTAGONISTS FOR THE TREATMENT OR THE PREVENTION OF PAIN DISORDERS INSERM - Institut National de la Santé et de la Recherche Médicale (FR) 2012-11-14 — — EP disclosed
US-20120258081-A1 METHODS OF TREATING PROLIFERATIVE DISEASES AMBIT BIOSCIENCES CORPORATION (US) 2012-10-11 — — US disclosed
EP-2429524-A1 METHODS OF TREATING PROLIFERATIVE DISEASES Ambit Biosciences Corporation (US) 2012-03-21 — — EP disclosed
WO-2011083124-A1 FLT3 RECEPTOR ANTAGONISTS FOR THE TREATMENT OR THE PREVENTION OF PAIN DISORDERS INSERM (Institut National de la Santé et de la Recherche Médicale) (FR) 2011-07-14 — — WO disclosed
WO-2010132787-A1 METHODS OF TREATING PROLIFERATIVE DISEASES AMBIT BIOSCIENCES CORPORATION (US) 2010-11-18 — — 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 (7 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-11384076-B2 Synthesis, pharmacology and use of new and selective FMS-like tyrosine kinase 3 (FLT3) FLT3 inhibitors FLT3, CSF3R, ABL1 FLT3 1/4885KDR 48/4885ABL1 3/4885
US-20150250720-A1 TABLET CONTAINING COMPOSITE WITH CYCLODEXTRIN HBZ, MCL1, HBB FLT3 23/4885KDR 4043/4885ABL1 99/4885
US-20260048099-A1 SYNERGISTIC INTERACTIONS FOR IMPROVED CANCER TREATMENT IL15RA, IL15, IL2RA FLT3 4/4885KDR 310/4885ABL1 399/4885
US-20120258081-A1 METHODS OF TREATING PROLIFERATIVE DISEASES FLT4, FLT1, CDK3 FLT3 6/4885KDR 57/4885ABL1 44/4885
US-20170216302-A1 METHOD FOR TREATING CANCER BY COMBINED USE FLT3, MDM2, TP53 FLT3 1/4885KDR 281/4885ABL1 5/4885
US-20130005966-A1 PROCESS FOR THE PREPARATION OF IMIDAZO[2,1-B][1,3]BENZOTHIAZOLE DERIVATIVES FLT4, FLT1, FLT3 FLT3 3/4885KDR 13/4885ABL1 132/4885
US-10716790-B2 Method for treating cancer by combined use FLT3, MDM2, TP53 FLT3 1/4885KDR 281/4885ABL1 5/4885

“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.

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