Succinic Acid

Succinic Acid

SCHEMBL679440

CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.O=C([O-])CCC(=O)[O-]

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB1CDK4CDK6CHRM2CHRM3DPP4DRD2DRD3DRD4EGFRHRH1HTR1BHTR1DHTR1FHTR2AHTR2CHTR4SLC6A2SLC6A4

The experimentally established mechanism targets of Succinic 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
CYP2C19 P33261 2/20 0.50
ALDH1A1 P00352 1/20 0.50
CYP1A2 P05177 1/20 0.50
CYP2D6 P10635 1/20 0.50
TSHR P16473 1/20 0.50
HDAC3 O15379 3/20 0.47
HDAC1 Q13547 3/20 0.47
HDAC2 Q92769 3/20 0.47
HDAC8 Q9BY41 3/20 0.47
HDAC4 P56524 1/20 0.47
HDAC7 Q8WUI4 1/20 0.47
HDAC10 Q969S8 1/20 0.47
HDAC11 Q96DB2 1/20 0.47
HDAC6 Q9UBN7 1/20 0.47
HDAC9 Q9UKV0 1/20 0.47
HDAC5 Q9UQL6 1/20 0.47
HIF1A Q16665 1/20 0.41
CES2 O00748 4/20 0.40
CES1 P23141 4/20 0.40
CA1 P00915 1/20 0.39

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
Propionic Acid SCHEMBL1399930 0.90 CYP1A2 (0.47) CYP2C19ALDH1A1CYP1A2CYP2D6TSHR
Bicarbonate SCHEMBL11663344 0.90 CYP1A2 (0.50) CYP2C19ALDH1A1CYP1A2CYP2D6TSHR
Bicarbonate SCHEMBL1144353 0.90 CYP1A2 (0.50) CYP2C19ALDH1A1CYP1A2CYP2D6TSHR
Acetic Acid SCHEMBL328882 0.88 TSHR (0.48) CYP2C19ALDH1A1CYP1A2CYP2D6TSHR
Oxalic Acid SCHEMBL10577823 0.88 CYP1A2 (0.48) CYP2C19ALDH1A1CYP1A2CYP2D6TSHR
Acetic Acid SCHEMBL133341 0.88 TSHR (0.48) CYP2C19ALDH1A1CYP1A2CYP2D6TSHR
Stearic Acid SCHEMBL11514728 0.88 CES2 (0.53) CES2CES1CA1PPARG
Acetic Acid SCHEMBL328881 0.86 TSHR (0.47) CYP2C19ALDH1A1CYP1A2CYP2D6TSHR
Acetic Acid SCHEMBL9467718 0.86 TSHR (0.47) CYP2C19ALDH1A1CYP1A2CYP2D6TSHR
Acetic Acid SCHEMBL10484555 0.86 CYP1A2 (0.47) CYP2C19ALDH1A1CYP1A2CYP2D6TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2954011-A1 ULTRA LOW CURE POWDER COATING Valspar Sourcing, Inc. (US) 2015-12-16 EP claimed
EP-2585473-B1 METAL PHOSPHONATE FLAME RETARDANT AND METHOD PRODUCING THEREOF ICL IP AMERICA INC (US) 2015-09-23 EP claimed
EP-2510035-B1 HYDROXYL-FUNCTIONAL POLYESTER RESINS DOW GLOBAL TECHNOLOGIES LLC (US) 2015-08-05 EP claimed
US-8975343-B2 Hydroxyl-functional polyester resins DOW GLOBAL TECHNOLOGIES LLC (US) 2015-03-10 US claimed
US-20150024194-A1 ULTRA LOW CURE POWDER COATINGS VALSPAR SOURCING, INC. (US) 2015-01-22 US claimed
US-8889773-B2 Metal phosphonate flame retardant and method producing thereof ICL-IP AMERICA INC. (US) 2014-11-18 US claimed
WO-2014123534-A1 ULTRA LOW CURE POWDER COATING VALSPAR SOURCING, INC. (US) 2014-08-14 WO claimed
US-20130165564-A1 METAL PHOSPHONATE FLAME RETARDANT AND METHOD PRODUCING THEREOF ICL-IP AMERICA INC. (US) 2013-06-27 US claimed
WO-2013077989-A1 PROCESS FOR PREPARATION OF ALUMINUM SALT OF PHOSPHONIC ACID ESTER ICL-IP AMERICA INC. (US) 2013-05-30 WO claimed
EP-2585473-A2 METAL PHOSPHONATE FLAME RETARDANT AND METHOD PRODUCING THEREOF ICL-IP America Inc. (US) 2013-05-01 EP claimed
US-6555628-B2 Controlled conversion resins derived from reacting epoxy resin, dihydric phenol, acid anhydride, and/or amine; protective/powder coatings DOW GLOBAL TECHNOLOGIES INC. 2003-04-29 US claimed
US-20020128428-A1 Epoxy resins and process for making the same DOW DEUTSCHLAND INC. (DE) 2002-09-12 US claimed
WO-2002048234-A2 EPOXY RESINS AND PROCESS FOR MAKING THE SAME DOW GLOBAL TECHNOLOGIES INC. (US) 2002-06-20 WO claimed
US-6284845-B1 POWDERED COATING COMPOSITION WHICH INCLUDES A CARBOXYL TERMINATED POLYESTER, EPOXY COMPOUNDS AND AN ONIUM CATALYST OR BETA-HYDROXYALKYLAMIDE MCWHORTER TECHNOLOGIES 2001-09-04 US claimed
US-5637654-A ONIUM CURING CATALYST; LOW TEMPERATURE CURING, HARDNESS, FLEXIBILITY MCWHORTER TECHNOLOGIES (US) 1997-06-10 US claimed
WO-1993004122-A1 POLYESTER COMPOSITIONS CONTAINING PHOSPHONIUM COMPOUNDS THE DOW CHEMICAL COMPANY (US) 1993-03-04 WO claimed
EP-0065564-B1 METHOD FOR PREPARING HIGH MOLECULAR WEIGHT EPOXY RESINS CONTAINING HYDROLYZED GLYCIDYL GROUPS THE DOW CHEMICAL COMPANY (US) 1986-04-02 EP claimed
EP-0111562-A4 PROCESS FOR PREPARING ADVANCED EPOXY RESINS EMPLOYING A PHOSPHONIUM TRIFLUOROACETATE CATALYST. DOW CHEMICAL CO (US) 1984-10-16 EP claimed
EP-0111562-A1 PROCESS FOR PREPARING ADVANCED EPOXY RESINS EMPLOYING A PHOSPHONIUM TRIFLUOROACETATE CATALYST THE DOW CHEMICAL COMPANY (US) 1984-06-27 EP claimed
WO-1984000171-A1 PROCESS FOR PREPARING ADVANCED EPOXY RESINS EMPLOYING A PHOSPHONIUM TRIFLUOROACETATE CATALYST DOW CHEMICAL CO (US) 1984-01-19 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 (1 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-20130165564-A1 METAL PHOSPHONATE FLAME RETARDANT AND METHOD PRODUCING THEREOF MTAP, AS3MT, MPHOSPH6 CYP2C19 3855/4885ALDH1A1 2973/4885CYP1A2 4254/4885

“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.