Pyridoxal Phosphate Anhydrous

Pyridoxal Phosphate Anhydrous

SCHEMBL827100

Cc1ncc(COP(=O)(O)O)c(C=O)c1O.O

nearest known ligand 0.97

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Pyridoxal Phosphate Anhydrous. 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
ESR1 known ✓ P03372 1/20 0.97
PTGS1 known ✓ P23219 1/20 0.97
PDE4A known ✓ P27815 1/20 0.97
MEN1 known ✓ O00255 2/20 0.60
P2RX2 Q9UBL9 3/20 0.97
ACP1 P24666 1/20 0.97
P2RX1 P51575 1/20 0.97
KDM4E B2RXH2 3/20 0.60
ALDH1A1 P00352 2/20 0.60
HPGD P15428 2/20 0.60
KMT2A Q03164 2/20 0.60
PNPO Q9NVS9 1/20 0.60
LMNA P02545 1/20 0.60
AOX1 Q06278 1/20 0.60
TRIM24 O15164 1/20 0.58
TRIM33 Q9UPN9 1/20 0.58
P2RX7 Q99572 2/20 0.44
YWHAG P61981 1/20 0.44
YWHAZ P63104 1/20 0.44
PDXK O00764 1/20 0.42

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
Pyridoxal Phosphate Anhydrous SCHEMBL29392551 1.00 P2RX2 (0.97) P2RX2ESR1PTGS1ACP1PDE4A
Pyridoxal Phosphate Anhydrous SCHEMBL23158 0.99 P2RX2 (1.00) P2RX2ESR1PTGS1ACP1PDE4A
Pyridoxal Phosphate Anhydrous SCHEMBL29362986 0.99 P2RX2 (1.00) P2RX2ESR1PTGS1ACP1PDE4A
Pyridoxal Phosphate Anhydrous SCHEMBL20335524 0.97 P2RX2 (0.97) P2RX2ESR1PTGS1ACP1PDE4A
Pyridoxal Phosphate Anhydrous SCHEMBL20335516 0.97 P2RX2 (0.97) P2RX2ESR1PTGS1ACP1PDE4A
Pyridoxal Phosphate Anhydrous SCHEMBL4916108 0.97 P2RX2 (0.97) P2RX2ESR1PTGS1ACP1PDE4A
Pyridoxal Phosphate Anhydrous SCHEMBL2746592 0.97 P2RX2 (0.97) P2RX2ESR1PTGS1ACP1PDE4A
Pyridoxal Phosphate Anhydrous SCHEMBL28200961 0.93 ESR1 (0.90) P2RX2ESR1PTGS1ACP1PDE4A
Pyridoxal Phosphate Anhydrous SCHEMBL29424718 0.92 P2RX2 (0.88) P2RX2ESR1PTGS1ACP1PDE4A
Pyridoxal Phosphate Anhydrous SCHEMBL10534222 0.92 P2RX2 (0.88) P2RX2ESR1PTGS1ACP1PDE4A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12310936-B2 Pharmaceutical compositions for the treatment of cancer SELEQ OY (FI) 2025-05-27 US claimed
CN-116615337-B Method and kit for three-dimensional (3D) printing 佩里多特打印有限责任公司 2025-04-18 CN claimed
US-20230416252-A1 PROCESS TOWARD THE MANUFACTURE OF (6R,10S)-10-{4-[5-CHLORO-2-(4-CHLORO-1H-1,2,3-TRIAZOL-1-YL)PHENYL]-6-OXO-1(6H)-PYRIMIDINYL}- 1-(DIFLUOROMETHYL)-6-METHYL-1,4,7,8,9,10-HEXAHYDRO-11,15-(METHENO)PYRAZOLO[4,3-B][1,7]DIAZACYCLOTETRADECIN-5(6H)-ONE JANSSEN PHARMACEUTICA NV (BE) 2023-12-28 US claimed
US-20230391000-A1 THREE-DIMENSIONAL PRINTING PERIDOT PRINT LLC 2023-12-07 US claimed
CN-117120418-A Process for the preparation of compound (I) 百时美施贵宝公司 2023-11-24 CN claimed
EP-4237224-A1 THREE-DIMENSIONAL PRINTING Hewlett-Packard Development Company, L.P. (US) 2023-09-06 EP claimed
CN-110777190-B Kit for detecting homocysteine and application thereof 武汉市长立生物技术有限责任公司 2023-08-22 CN claimed
CN-116615337-A Three-dimensional printing 惠普发展公司,有限责任合伙企业 2023-08-18 CN claimed
EP-4225757-A1 A PROCESS TOWARD THE MANUFACTURE OF (6R,10S)-10-{4-[5-CHLORO-2-(4-CHLORO-1H-1,2,3-TRIAZOL-1-YL)PHENYL]-6-OXO-1(6H)-PYRIMIDINYL}-1-(DIFLUOROMETHYL)-6-METHYL-1,4,7,8,9,10-HEXAHYDRO-11,15-(METHENO)PYRAZOLO[4,3-B] [1,7]DIAZACYCLOTETRADECIN-5(6H)-ONE Bristol-Myers Squibb Company (US) 2023-08-16 EP claimed
US-20220235313-A1 MYCOPLASMA MEDIA FORMULATIONS ELANCO US INC. 2022-07-28 US claimed
EP-2300598-B1 USE AND METHODS FOR PREVENTING AND/OR TREATING ORAL MALODOUR BASF SE (DE) 2016-04-13 EP claimed
US-8142800-B1 Oral high potency clinical anti-craving treatment and method of use REAL SUBSTANCE SOLUTIONS, INC. 2012-03-27 US claimed
US-8142799-B2 High potency clinical anti-craving treatment and method of use REAL SUBSTANCE SOLUTIONS, INC. 2012-03-27 US claimed
US-20050287226-A1 High potency clinical anti-craving treatment and method of use REAL SUBSTANCE SOLUTIONS, INC. 2005-12-29 US claimed
EP-0743574-B1 Migration imaging members XEROX CORP (US) 2000-12-27 EP claimed
EP-0743573-B1 Method for obtaining image contrast migration imaging members XEROX CORP (US) 2000-09-06 EP claimed
EP-0743574-A2 Migration imaging members XEROX CORPORATION (US) 1996-11-20 EP claimed
EP-0743573-A2 Method for obtaining image contrast migration imaging members XEROX CORPORATION (US) 1996-11-20 EP claimed
US-5563014-A SOFTENABLE LAYER CONTAINIG PHOTOSENSITIVE MARKING MATERIAL; TRANSPARENTIZING AGENT XEROX CORPORATION (US) 1996-10-08 US claimed
US-5514505-A SELECTIVE TRANSPARENTIZATION OF PHOTOSENSITIVE MIGRATION MARKING PARTICLES EMBEDDED NEAR THE SURFACE OF A SOFTENABLE LAYER SUPPORTED BY AN ELECTROCONDUCTIVE SUBSTRATE XEROX CORPORATION (US) 1996-05-07 US 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.

PatentTitleText reads most aboutPredicted target · text-rank
US-20230416252-A1 PROCESS TOWARD THE MANUFACTURE OF (6R,10S)-10-{4-[5-CHLORO-2-(4-CHLORO-1H-1,2,3-TRIAZOL-1-YL)PHENYL]-6-OXO-1(6H)-PYRIMIDINYL}- 1-(DIFLUOROMETHYL)-6-METHYL-1,4,7,8,9,10-HEXAHYDRO-11,15-(METHENO)PYRAZOLO[4,3-B][1,7]DIAZACYCLOTETRADECIN-5(6H)-ONE CYP1B1, AZI2, TET1 ESR1 4748/4885PTGS1 248/4885PDE4A 2739/4885
US-12310936-B2 Pharmaceutical compositions for the treatment of cancer RNASE1, SELENOI, GLS2 ESR1 2847/4885PTGS1 3553/4885PDE4A 3186/4885

“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.