Known targets — ChEMBL curated mechanism
ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Alizarin Red. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 6)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | PKLR | P30613 | 13/20 | 1.00 |
| ▸ | PGAM1 | P18669 | 7/20 | 1.00 |
| ▸ | PTPN1 | P18031 | 2/20 | 1.00 |
| ▸ | BCL2 | P10415 | 1/20 | 0.60 |
| ▸ | MCL1 | Q07820 | 1/20 | 0.60 |
| ▸ | TTR | P02766 | 1/20 | 0.51 |
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 | |
|---|---|---|---|---|
| Alizarin Red SCHEMBL29368828 | 1.00 | PKLR (1.00) | PKLRPGAM1PTPN1BCL2MCL1 | |
| Alizarin Red SCHEMBL728494 | 1.00 | PKLR (1.00) | PKLRPGAM1PTPN1BCL2MCL1 | |
| Alizarin Red SCHEMBL29534709 | 0.98 | PKLR (0.97) | PKLRPGAM1PTPN1BCL2MCL1 | |
| Alizarin Red SCHEMBL1203855 | 0.83 | PGAM1 (1.00) | PKLRPGAM1PTPN1BCL2MCL1 | |
| Alizarin Red SCHEMBL29630358 | 0.83 | PGAM1 (1.00) | PKLRPGAM1PTPN1BCL2MCL1 | |
| Alizarin Red SCHEMBL29372853 | 0.83 | PGAM1 (1.00) | PKLRPGAM1PTPN1BCL2MCL1 | |
| Alizarin Red SCHEMBL433811 | 0.82 | PGAM1 (0.97) | PKLRPGAM1PTPN1BCL2MCL1 | |
| SCHEMBL1506814 | 0.82 | PGAM1 (0.73) | PKLRPGAM1PTPN1BCL2MCL1 | |
| SCHEMBL12304032 | 0.82 | PGAM1 (0.73) | PKLRPGAM1PTPN1BCL2MCL1 | |
| Alizarin Red SCHEMBL728495 | 0.82 | PGAM1 (0.97) | PKLRPGAM1PTPN1BCL2MCL1 |
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 1939 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122070479-A | Ultrasonic indicating device and method for monitoring ultrasonic treatment | JP实验室股份有限公司 | 2026-05-19 | — | — | CN | claimed |
| US-20260055703-A1 | BRIDGE SENSOR DESIGN FOR WATER AND OIL ANALYSIS IN FORMATION TESTING | HALLIBURTON ENERGY SERVICES, INC. (US) | 2026-02-26 | — | — | US | claimed |
| US-20260028685-A1 | Saliva Stabilization Solution For Use In Nucleic Acid Amplification Reactions And Methods Of Use For The Detection Of Pathogen Nucleic Acids | UNIV COLORADO REGENTS (US) | 2026-01-29 | — | — | US | claimed |
| EP-4661729-A1 | METHOD FOR OPERATING A DISHWASHER WITH A MEASUREMENT UNIT FOR MEASURING A PH-VALUE OF THE WASHING LIQUOR | V-Zug AG (CH) | 2025-12-17 | — | — | EP | claimed |
| US-12492633-B2 | Bridge sensor design for water and oil analysis in formation testing | HALLIBURTON ENERGY SERVICES, INC. (US) | 2025-12-09 | — | — | US | claimed |
| EP-4612342-A1 | RECOVERY OF ENERGY CRITICAL HIGH VALUE METALS USING FUNCTIONALIZED MATERIALS | Cornell University (US) | 2025-09-10 | — | — | EP | claimed |
| WO-2025122600-A1 | COMPOSITIONS AND METHODS FOR TREATING ABERRANT NITROSYLATION | CASE WESTERN RESERVE UNIVERSITY (US) | 2025-06-12 | — | — | WO | claimed |
| CN-120064256-A | High-sensitivity glucose colorimetric detector and preparation method thereof | 大连理工大学 | 2025-05-30 | — | — | CN | claimed |
| CN-120024903-A | Method for purifying chlorosilane by physical adsorption and coordination | 木林森活性炭江苏有限公司 | 2025-05-23 | — | — | CN | claimed |
| WO-2025090061-A1 | ULTRASONIC INDICATOR DEVICE AND METHOD FOR MONITORING ULTRASONICATION | JP LABORATORIES, INC. (US) | 2025-05-01 | — | — | WO | claimed |
| CN-111269202-B | Preparation method of 2, 5-furan diformaldehyde under illumination condition | 南京林业大学 | 2022-04-15 | — | — | CN | claimed |
| CN-114276573-A | High-durability organic antioxidant chelated cerium ion composite proton exchange membrane and preparation method and application thereof | 上海应用技术大学 | 2022-04-05 | — | — | CN | claimed |
| CN-114199652-A | Method for rapidly preparing rock slices on drilling site | 中海油能源发展股份有限公司 | 2022-03-18 | — | — | CN | claimed |
| US-20220065794-A1 | SYSTEM AND METHOD FOR LOGISTICS MANAGEMENT BASED ON ODOR MOLECULES | TAIWAN CARBON NANO TECHNOLOGY CORPORATION (TW) | 2022-03-03 | — | — | US | claimed |
| US-20220064469-A1 | WRITING AND/OR DRAWING SYSTEM COMPRISING PH SENSITIVE DYE AND METHOD THEREOF | SANKO TEKSTIL ISLETMELERI SAN VE TIC AS (TR) | 2022-03-03 | — | — | US | claimed |
| CN-114118197-A | System and method for carrying out logistics management based on odor molecules | 台湾奈米碳素股份有限公司 | 2022-03-01 | — | — | CN | claimed |
| CN-112301398-B | Preparation method of golden film | 九牧厨卫股份有限公司 | 2022-02-18 | — | — | CN | claimed |
| CN-109991294-B | Membrane electrode, preparation method thereof, sensor using membrane electrode, electrochemical workstation and application of electrochemical workstation | 南京腾森分析仪器有限公司 | 2022-02-18 | — | — | CN | claimed |
| US-11237113-B2 | Rapid pH measurement | ESSENLIX CORPORATION (US) | 2022-02-01 | — | — | US | claimed |
| WO-2022020379-A1 | GUN SHOT RESIDUE FIELD KIT | VERITEQUE USA, INC. (US) | 2022-01-27 | — | — | WO | claimed |
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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20260028685-A1 | Saliva Stabilization Solution For Use In Nucleic Acid Amplification Reactions And Methods Of Use For The Detection Of Pathogen Nucleic Acids | RNASEH1, ACE2, DDX42 | PKLR 3332/4885PGAM1 2075/4885PTPN1 2347/4885 |
| US-20260055703-A1 | BRIDGE SENSOR DESIGN FOR WATER AND OIL ANALYSIS IN FORMATION TESTING | FLNB, DVL1, DSG1 | PKLR 3080/4885PGAM1 3408/4885PTPN1 3960/4885 |
“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.