Hydrochloric Acid

Hydrochloric Acid

SCHEMBL987360

Cl.O=S(=O)(Cl)c1cccc2cnccc12

nearest known ligand 0.57

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
PRKD3 known ✓ O94806 7/20 0.55
PRKCG known ✓ P05129 7/20 0.55
PRKCB known ✓ P05771 7/20 0.55
PRKCA known ✓ P17252 7/20 0.55
PRKCH known ✓ P24723 7/20 0.55
PRKCI known ✓ P41743 7/20 0.55
PRKCE known ✓ Q02156 7/20 0.55
PRKCQ known ✓ Q04759 7/20 0.55
PRKCZ known ✓ Q05513 7/20 0.55
PRKCD known ✓ Q05655 7/20 0.55
PRKD1 known ✓ Q15139 7/20 0.55
GLA known ✓ P06280 1/20 0.54
ROCK2 known ✓ O75116 5/20 0.51
ROCK1 known ✓ Q13464 5/20 0.51
HTR1A known ✓ P08908 1/20 0.49
ADRA2A known ✓ P08913 1/20 0.49
ADRA2B known ✓ P18089 1/20 0.49
SLC6A4 known ✓ P31645 1/20 0.49
HRH1 known ✓ P35367 1/20 0.49
OPRK1 known ✓ P41145 1/20 0.49

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 SCHEMBL29469852 1.00 LMNA (0.57) LMNAMEN1KMT2ASMN1; SMN2PMP22
SCHEMBL115053 0.98 CYP3A4 (0.56) LMNAMEN1KMT2ASMN1; SMN2PMP22
SCHEMBL29546384 0.98 CYP3A4 (0.56) LMNAMEN1KMT2ASMN1; SMN2PMP22
SCHEMBL28592488 0.87 PRKD3 (0.49) LMNAMEN1KMT2ASMN1; SMN2PMP22
SCHEMBL28586335 0.85 PRKCZ (0.62) LMNAMEN1KMT2ASMN1; SMN2PMP22
SCHEMBL3129943 0.84 TNF (0.46) LMNAMEN1KMT2ASMN1; SMN2PMP22
SCHEMBL30002842 0.84 TNF (0.46) LMNAMEN1KMT2ASMN1; SMN2PMP22
SCHEMBL6967362 0.84 CYP3A4 (0.59) LMNAMEN1KMT2ASMN1; SMN2PMP22
SCHEMBL28591143 0.83 PRKD3 (0.49) LMNAMEN1KMT2ASMN1; SMN2PMP22
Hydrochloric Acid SCHEMBL8670953 0.83 LMNA (0.57) LMNAMEN1KMT2ASMN1; SMN2PMP22

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116924985-A Preparation method of fasudil 山东新时代药业有限公司 2023-10-24 CN claimed
CN-113358761-B Detection method of 5-isoquinoline sulfonic acid 昆药集团股份有限公司 2023-05-16 CN claimed
CN-113358762-B Method for detecting related substances in 5-isoquinoline sulfonyl chloride hydrochloride 昆药集团股份有限公司 2023-04-07 CN claimed
CN-111909088-B Method for preparing isoquinoline hydrochloride intermediate and Rho kinase inhibitor by using BTC/Ph3PO chloro-system 浙江工业大学 2022-03-01 CN claimed
CN-113968816-A Preparation method of isoquinoline-5-sulfonyl chloride hydrochloride 合肥久诺医药科技有限公司 2022-01-25 CN claimed
CN-113358762-A Method for detecting related substances in 5-isoquinoline sulfonyl chloride hydrochloride 昆药集团股份有限公司 2021-09-07 CN claimed
CN-110441449-B Method for detecting related substances in fasudil hydrochloride raw material or injection 昆药集团股份有限公司 2021-06-29 CN claimed
CN-111909088-A Utilizing BTC/Ph3Method for preparing isoquinoline hydrochloride intermediate and Rho kinase inhibitor by PO chloro system 浙江工业大学 2020-11-10 CN claimed
CN-109574992-B Preparation method of fasudil hydrochloride 河南润弘制药股份有限公司 2020-05-22 CN claimed
CN-110441449-A In relation to the detection method of substance in Fasudic hydrochloride raw material or injection KPC PHARMACEUTICALS INC 2019-11-12 CN claimed
CN-109970712-A A kind of refining methd of Fasudic hydrochloride 徐州万邦金桥制药有限公司 2019-07-05 CN claimed
CN-109574992-A A kind of preparation method of Fasudic hydrochloride 河南润弘制药股份有限公司 2019-04-05 CN claimed
CN-105866263-A Quality control method for fasudil hydrochloride 四川升和药业股份有限公司 2016-08-17 CN claimed
CN-103450157-B Preparation method for high-purity hydroxyfasudil semihydrate HEFEI JIUNUO MEDICAL TECHNOLOGY CO LTD 2015-03-18 CN claimed
JP-11158177-A None JP disclosed
JP-11171885-A None JP disclosed
US-12630529-B2 GCN2 modulator compounds Alesta Therapeutics BV (NL) 2026-05-19 US disclosed
EP-0287696-A1 Isoquinoline derivatives Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1988-10-26 EP disclosed
US-4678783-A CARDIOVASCULAR DISORDERS, HYPOTENSIVES, ARTERIOSCLEROSIS ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1987-07-07 US disclosed
EP-0187371-A2 Substituted isoquinolinesulfonyl compounds Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1986-07-16 EP 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 (1 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-12630529-B2 GCN2 modulator compounds NR3C1, GCN1, EIF2AK4 PRKD3 1298/4885PRKCG 2154/4885PRKCB 1543/4885

“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.