Known targets — ChEMBL curated mechanism
ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA
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)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | NPC1 | O15118 | 1/20 | 0.65 |
| ▸ | RAB9A | P51151 | 1/20 | 0.65 |
| ▸ | ATM | Q13315 | 1/20 | 0.65 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.49 |
| ▸ | CYP1A2 | P05177 | 2/20 | 0.47 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.47 |
| ▸ | MAPK1 | P28482 | 2/20 | 0.47 |
| ▸ | HIF1A | Q16665 | 2/20 | 0.47 |
| ▸ | GPR35 | Q9HC97 | 2/20 | 0.47 |
| ▸ | TSHR | P16473 | 2/20 | 0.47 |
| ▸ | TP53 | P04637 | 1/20 | 0.47 |
| ▸ | HPGD | P15428 | 1/20 | 0.47 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.47 |
| ▸ | TXNRD1 | Q16881 | 1/20 | 0.46 |
| ▸ | TXNRD3 | Q86VQ6 | 1/20 | 0.46 |
| ▸ | TXNRD2 | Q9NNW7 | 1/20 | 0.46 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.46 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.46 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.46 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.46 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL31173710 | 1.00 | NPC1 (0.65) | NPC1RAB9AATMTDP1CYP1A2 | |
| SCHEMBL741714 | 0.98 | NPC1 (0.62) | NPC1RAB9AATMTDP1CYP1A2 | |
| Hydrochloric Acid SCHEMBL10444520 | 0.97 | NPC1 (0.61) | NPC1RAB9AATMTDP1CYP1A2 | |
| Thiocyanic Acid SCHEMBL6501837 | 0.90 | NPC1 (0.54) | NPC1RAB9AATMTDP1CYP1A2 | |
| Hydrochloric Acid SCHEMBL8068701 | 0.88 | NPC1 (0.67) | NPC1RAB9AATMTDP1CYP1A2 | |
| SCHEMBL741713 | 0.87 | NPC1 (0.51) | NPC1RAB9AATMTDP1CYP1A2 | |
| Hydrochloric Acid SCHEMBL30343291 | 0.87 | NPC1 (0.65) | NPC1RAB9AATMTDP1CYP1A2 | |
| Hydrochloric Acid SCHEMBL599994 | 0.87 | NPC1 (0.65) | NPC1RAB9AATMTDP1CYP1A2 | |
| Hydrochloric Acid SCHEMBL10444521 | 0.86 | NPC1 (0.50) | NPC1RAB9AATMTDP1CYP1A2 | |
| SCHEMBL29618182 | 0.86 | RAB9A (0.64) | NPC1RAB9AATMTDP1CYP1A2 |
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 65 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20230100211-A1 | PROCESS FOR THE PREPARATION OF SODIUM 4-(2-((1E,3E,5E,7Z)-7-(1,1-DIMETHYL-3-(4-SULFONATOBUTYL)-1H-BENZO[e]INDOL-2(3H)-YLIDENE) HEPTA-1,3,5-TRIENYL)-1,1-DIMETHYL-1H-BENZO[e]INDOLIUM-3-YL) BUTANE-1-SULFONATE (INDOCYANINE GREEN) | BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. (IN) | 2023-03-30 | — | — | US | claimed |
| US-20190337896-A1 | PROCESS FOR THE PREPARATION OF SODIUM 4-(2-((1E,3E,5E,7Z)-7-(1,1-DIMETHYL-3-(4-SULFONATOBUTYL)-1H-BENZO[e]INDOL-2(3H)-YLIDENE) HEPTA-1,3,5-TRIENYL)-1,1-DIMETHYL-1H-BENZO[e]INDOLIUM-3-YL) BUTANE-1-SULFONATE (INDOCYANINE GREEN) | BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. (IN) | 2019-11-07 | — | — | US | claimed |
| EP-1015663-A1 | CORROSION INHIBITION THROUGH THE USE OF A QUATERNARY PYRIDINE SALT-HYDROCARBON COMBINATION | Stanchem Inc. (CA) | 2000-07-05 | — | — | EP | claimed |
| WO-1998033953-A1 | CORROSION INHIBITION THROUGH THE USE OF A QUATERNARY PYRIDINE SALT-HYDROCARBON COMBINATION | STANCHEM INC. (CA) | 1998-08-06 | — | — | WO | claimed |
| EP-0117196-B1 | DERIVATIVES OF N-IMINOPYRIDINIUM BETAINES, THEIR PREPARATION AND THEIR USE AS MEDICAMENTS | PROVESAN S.A. (CH) | 1986-07-30 | — | — | EP | claimed |
| EP-4680678-A1 | MECHANOCHEMICAL PROCESS FOR SYNTHESISING A CYANINE COMPOUND | The University of Sussex (GB) | 2026-01-21 | — | — | EP | disclosed |
| WO-2024189210-A1 | MECHANOCHEMICAL PROCESS FOR SYNTHESISING A CYANINE COMPOUND | THE UNIVERSITY OF SUSSEX (GB) | 2024-09-19 | — | — | WO | disclosed |
| US-20230380264-A1 | ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES | UNIVERSAL DISPLAY CORPORATION | 2023-11-23 | — | — | US | disclosed |
| US-11746426-B2 | Stabilization of a co-bound intermediate via molecular tuning promotes CO2-to-ethylene conversion | CALIFORNIA INSTITUTE OF TECHNOLOGY (US) | 2023-09-05 | — | — | US | disclosed |
| US-20230100211-A1 | PROCESS FOR THE PREPARATION OF SODIUM 4-(2-((1E,3E,5E,7Z)-7-(1,1-DIMETHYL-3-(4-SULFONATOBUTYL)-1H-BENZO[e]INDOL-2(3H)-YLIDENE) HEPTA-1,3,5-TRIENYL)-1,1-DIMETHYL-1H-BENZO[e]INDOLIUM-3-YL) BUTANE-1-SULFONATE (INDOCYANINE GREEN) | BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. (IN) | 2023-03-30 | — | — | US | disclosed |
| EP-2905361-B1 | METHOD OF FORMING A METAL COATING | TOYOTA MOTOR CO LTD (JP) | 2022-01-05 | — | — | EP | disclosed |
| WO-2021007508-A9 | THE STABILIZATION OF A CO-BOUND INTERMEDIATE VIA MOLECULAR TUNING PROMOTES CO2-TO-ETHYLENE CONVERSION | CALIFORNIA INSTITUTE OF TECHNOLOGY (US) | 2021-11-18 | — | — | WO | disclosed |
| US-4594312-A | Photothermographic medium | MINNESOTA MINING AND MANUFACTURING COMPANY (US) | 1986-06-10 | — | — | US | disclosed |
| US-4563467-A | ANTIEDEMIC, LACTATION BLOCKERS | PROVESAN S.A. (CH) | 1986-01-07 | — | — | US | disclosed |
| EP-0120601-A2 | Oxidative imaging | MINNESOTA MINING AND MANUFACTURING COMPANY (US) | 1984-10-03 | — | — | EP | disclosed |
| EP-0119831-A2 | Heat bleachable dye systems | MINNESOTA MINING AND MANUFACTURING COMPANY (US) | 1984-09-26 | — | — | EP | disclosed |
| US-4218432-A | Coloring agent and a composition including the same for coloring toilet bowl flushing water | YAMAMOTO KAGAKU GOSEI CO., LTD. (JP) | 1980-08-19 | — | — | US | disclosed |
| US-4088653-A | FROM A CARBONYLHYDRAZIDE AND AN ARYL-PYRIDINIUM HALIDE, REDUCTION WITH A BOROHYDRIDE; ANALGESICS, ANTIINFLAMMATORY AND HYPERGLYCEMIC AGENTS | CANADIAN PATENTS AND DEVELOPMENTS LIMITED (CA) | 1978-05-09 | — | — | US | disclosed |
| US-4010156-A | Process for the rearrangement of penicillins to cephalosporins and intermediate compounds thereof | AMERICAN HOME PRODUCTS CORPORATION (US) | 1977-03-01 | — | — | US | disclosed |
| US-3932398-A | 3-Halo-cepham derivatives | AMERICAN HOME PRODUCTS CORPORATION (US) | 1976-01-13 | — | — | 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 (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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20190337896-A1 | PROCESS FOR THE PREPARATION OF SODIUM 4-(2-((1E,3E,5E,7Z)-7-(1,1-DIMETHYL-3-(4-SULFONATOBUTYL)-1H-BENZO[e]INDOL-2(3H)-YLIDENE) HEPTA-1,3,5-TRIENYL)-1,1-DIMETHYL-1H-BENZO[e]INDOLIUM-3-YL) BUTANE-1-SULFONATE (INDOCYANINE GREEN) | SULT1E1, IK, SULT1A1 | NPC1 1516/4885RAB9A 1251/4885ATM 4613/4885 |
| US-20230100211-A1 | PROCESS FOR THE PREPARATION OF SODIUM 4-(2-((1E,3E,5E,7Z)-7-(1,1-DIMETHYL-3-(4-SULFONATOBUTYL)-1H-BENZO[e]INDOL-2(3H)-YLIDENE) HEPTA-1,3,5-TRIENYL)-1,1-DIMETHYL-1H-BENZO[e]INDOLIUM-3-YL) BUTANE-1-SULFONATE (INDOCYANINE GREEN) | SULT1E1, IK, SULT1A1 | NPC1 1516/4885RAB9A 1251/4885ATM 4613/4885 |
| US-20230380264-A1 | ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES | TIMCC, ICOSLG, NUDT1 | NPC1 3889/4885RAB9A 3729/4885ATM 4237/4885 |
“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.