Alizarin Red

Alizarin Red

SCHEMBL728494

O=C1c2ccccc2C(=O)c2c1cc(S(=O)(=O)[O-])c(O)c2O.[Na+]

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

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)

geneUniProtsupporting neighboursconfidence
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.

Compoundsimilaritytop predictedshared targets
Alizarin Red SCHEMBL29368828 1.00 PKLR (1.00) PKLRPGAM1PTPN1BCL2MCL1
Alizarin Red SCHEMBL29349481 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 241 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117996232-A Additive for aqueous zinc ion battery electrolyte and application thereof 黑龙江大学 2024-05-07 CN claimed
CN-116199247-A Preparation method of boron-containing aluminum sol for coating ternary positive electrode material of lithium battery 福州大学 2023-06-02 CN claimed
CN-115433338-A Preparation method of water-soluble ultraviolet-curing matte hyperbranched polyurethane acrylic resin 武汉超支化树脂科技有限公司 2022-12-06 CN claimed
EP-3906338-A1 WRITING AND/OR DRAWING SYSTEM COMPRISING PH SENSITIVE DYE AND METHOD THEREOF Sanko Tekstil Isletmeleri San. Ve Tic. A.S. (TR) 2021-11-10 EP claimed
CN-113544327-A Writing and/or painting system comprising a pH sensitive dye and method thereof 尚科纺织企业工业及贸易公司 2021-10-22 CN claimed
CN-109107546-B Synthetic method and application of alizarin red-S chelating resin 河南省岩石矿物测试中心 2021-06-04 CN claimed
WO-2020141216-A1 WRITING AND/OR DRAWING SYSTEM COMPRISING PH SENSITIVE DYE AND METHOD THEREOF SANKO TEKSTIL ISLETMELERI SAN. VE TIC. A.S. (TR) 2020-07-09 WO claimed
CN-111097541-A Dye-sensitized black titanium dioxide and preparation method and application thereof 中国科学院上海硅酸盐研究所 2020-05-05 CN claimed
CN-109107546-A Synthetic method and application of alizarin red-S chelate forming resin 河南省岩石矿物测试中心 2019-01-01 CN claimed
CN-106576963-A Management method for promoting prematurity of potted butterfly orchid 安徽裕龙种植农民专业合作社 2017-04-26 CN claimed
CN-1332642-C Composition for self-diagnosis and reduction catalyst treatment of permanent and hair straightener and method of preparation BEEBONG FINE CO LTD (KR) 2007-08-22 CN claimed
CN-1879711-A A Chinese medicinal composition for treating gastric disease, its preparation process and quality control method GAO QINGCHUAN (CN) 2006-12-20 CN claimed
CN-1285370-C Pharmaceutical composition for treating gastritis, gastric ulcer and doudenal ulcer QINGDAO GROWFUL PHARMACEUTICAL (CN) 2006-11-22 CN claimed
CN-1758894-A Composition for self-diagnosis and reduction catalyst treatment of permanent and hair straightener and method of preparation BEEBONG FINE CO LTD (KR) 2006-04-12 CN claimed
CN-1730025-A Pharmaceutical composition for treating gastritis, gastric ulcer and doudenal ulcer QINGDAO GROWFUL PHARMACEUTICAL (CN) 2006-02-08 CN claimed
EP-0454058-B1 Use of anthraquinone derivatives in the prophylaxis and treatment of viral diseases LOHMANN RUDOLF LOMAPHARM (DE) 1998-06-17 EP claimed
EP-0498707-B1 Process of dyeing keratinous fibers with a mono- or di-hydroxyindole and a non-oxidative aromatic carbonyl derivative and dyeing agent OREAL (FR) 1995-08-02 EP claimed
US-5250385-A Photosensitivity, storage stability FUJI PHOTO FILM CO., LTD. (JP) 1993-10-05 US claimed
EP-0454058-A2 Use of anthraquinone derivatives in the prophylaxis and treatment of viral diseases LOMAPHARM Rudolf Lohmann GmbH KG Pharmazeutische Fabrik (DE) 1991-10-30 EP claimed
US-4522963-A Procedure for curing unsaturated polyester resins MUANYAGIPARI KUTATO INTEZET (HU) 1985-06-11 US claimed