Medronic Acid

Medronic Acid

SCHEMBL4605897

O=P([O-])([O-])CP(=O)(O)O.[Na+].[Na+]

nearest known ligand 0.56

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 Medronic 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
THRB known ✓ P10828 1/20 0.56
TYMS known ✓ P04818 1/20 0.35
KDM4E B2RXH2 2/20 0.56
MMP2 P08253 1/20 0.56
MAPK1 P28482 1/20 0.56
HSD17B10 Q99714 1/20 0.56
SLC34A1 Q06495 1/20 0.41
OTC P00480 1/20 0.41
KMT2A Q03164 2/20 0.36
CYP2C19 P33261 1/20 0.36
LMNA P02545 3/20 0.35
BTN3A1 O00481 2/20 0.34
MEN1 O00255 1/20 0.32
HPGD P15428 1/20 0.32
TSHR P16473 1/20 0.32
BLM P54132 1/20 0.32
TDP1 Q9NUW8 1/20 0.32
PGK1 P00558 1/20 0.32
PGK2 P07205 1/20 0.32
ALDH1A1 P00352 1/20 0.32

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
Medronic Acid SCHEMBL27363301 0.97 KDM4E (0.53) KDM4EMMP2THRBMAPK1HSD17B10
Medronic Acid SCHEMBL2638879 0.80 SLC34A1 (0.41) KDM4EMMP2THRBMAPK1HSD17B10
Medronic Acid SCHEMBL9457334 0.79 KDM4E (0.48) KDM4EMMP2THRBMAPK1HSD17B10
Medronic Acid SCHEMBL409013 0.78 LMNA (0.35) KDM4EMMP2THRBMAPK1HSD17B10
Medronic Acid SCHEMBL5272656 0.74 LMNA (0.33) SLC34A1LMNABTN3A1
Medronic Acid SCHEMBL66716 0.73
Medronic Acid SCHEMBL8350837 0.73 KDM4E (1.00) KDM4EMMP2THRBMAPK1HSD17B10
Medronic Acid SCHEMBL7929832 0.73 SLC34A1 (0.50) KDM4EMMP2THRBMAPK1HSD17B10
Medronic Acid SCHEMBL133343 0.72 SLC34A1 (0.47) KDM4EMMP2THRBMAPK1HSD17B10
Medronic Acid SCHEMBL5267588 0.70 SLC34A1 (0.43) KDM4EMMP2THRBMAPK1HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11674162-B2 Selective advantage in fermentation GINKGO BIOWORKS, INC. (US) 2023-06-13 US disclosed
CN-113631225-A Methods and systems for producing AAV particles 沃雅戈治疗公司 2021-11-09 CN disclosed
CN-103271083-B Multi-functional ionic liquid compositions 阿拉巴马大学 2017-08-11 CN disclosed
US-20170096691-A1 SELECTIVE ADVANTAGE IN FERMENTATION NOVOGY, INC. (US) 2017-04-06 US disclosed
WO-2015168534-A1 THERAPEUTIC TREATMENT OF GASTROINTESTINAL MICROBIAL IMBALANCES THROUGH COMPETITIVE MICROBE DISPLACEMENT NOVOGY, INC. (US) 2015-11-05 WO disclosed
EP-1328616-B2 STABILIZED LIQUID COMPOSITIONS PROCTER & GAMBLE (US) 2015-03-04 EP disclosed
EP-1978081-B1 Stabilized liquid compositions PROCTER & GAMBLE (US) 2014-04-30 EP disclosed
CN-103271083-A Multi-functional ionic liquid compositions UNIV ALABAMA 2013-09-04 CN disclosed
CN-101326275-B Multifunctional ionic liquid composition UNIV ALABAMA 2013-06-05 CN disclosed
CN-101326275-A Multifunctional ionic liquid composition UNIV ALABAMA (US) 2008-12-17 CN disclosed
CN-1251993-A Use of n-substituted-1,5-dideoxy-1,5-imino-d-glucitol compounds in combination therapy for treating hepatitis virus infections SEARLE & CO (US) 2000-05-03 CN disclosed
US-5534129-A Cyanidic-alkaline baths for the galvanic deposition of copper-tin alloy coatings, uses thereof, and metallic bases coated with said copper-tin alloy coating DEGUSSA AKTIENGESELLSCHAFT (DE) 1996-07-09 US disclosed
US-5006329-A Radioactive tagged compounds and method for the treatment of metastatic bone cancer CADEMA MEDICAL PRODUCTS, INC. (US) 1991-04-09 US disclosed
EP-0419264-A2 Aminophosphinates and polymers thereof and their use in detergent compositions Albright & Wilson Limited (GB) 1991-03-27 EP disclosed
US-4762649-A WATER TREATMENT, ANTISCALING, ANTICORROSION MONSANTO COMPANY (US) 1988-08-09 US disclosed
US-4719031-A ANTISCALE MONSANTO COMPANY (US) 1988-01-12 US disclosed
US-4663432-A ANTISCALING, CORROSION RESISTANCE MONSANTO COMPANY (US) 1987-05-05 US disclosed
US-4605474-A Alkaline cyanide bath for electrolytic deposition of copper-tin-alloy coatings HOFFACKER GERD (DE) 1986-08-12 US disclosed
US-4565608-A Alkaline cyanide bath for electrolytic deposition of copper-tin-alloy coatings DEGUSSA AKTIENGESELLSCHAFT (DE) 1986-01-21 US disclosed
US-4254114-A Control of pyrophosphate microorganisms with organophosphonates THE PROCTOR & GAMBLE COMPANY (US) 1981-03-03 US disclosed