Succinic Acid

Succinic Acid

SCHEMBL124833

CC(=O)O.O=C(O)CCC(=O)O.O=C(O)c1ccc(C(=O)O)c(C(=O)O)c1

nearest known ligand 0.53

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
KDM4E B2RXH2 4/20 0.53
HSD17B10 Q99714 3/20 0.50
CDC25A P30304 1/20 0.50
CDC25B P30305 1/20 0.50
TDP1 Q9NUW8 2/20 0.49
POLB P06746 2/20 0.49
L3MBTL1 Q9Y468 2/20 0.49
MYC P01106 1/20 0.45
KMT2A Q03164 1/20 0.43
ACE2 Q9BYF1 2/20 0.42
RAB9A P51151 2/20 0.42
LMNA P02545 1/20 0.42
AKR1C3 P42330 3/20 0.41
AKR1C2 P52895 3/20 0.41
HTT P42858 1/20 0.41
ALDH1A1 P00352 3/20 0.41
AKR1B10 O60218 1/20 0.41
AKR1B1 P15121 1/20 0.41
AKR1C4 P17516 1/20 0.41
AKR1C1 Q04828 1/20 0.41

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
Succinic Acid SCHEMBL4766771 0.94 KDM4E (0.58) KDM4EHSD17B10CDC25ACDC25BTDP1
Butyric Acid SCHEMBL27742018 0.91 KDM4E (0.49) KDM4EHSD17B10CDC25ACDC25BTDP1
Succinic Acid SCHEMBL8083564 0.91 KDM4E (0.55) KDM4EHSD17B10CDC25ACDC25BTDP1
Acetic Acid SCHEMBL28378441 0.90 KDM4E (0.62) KDM4EHSD17B10CDC25ACDC25BTDP1
Acetic Acid SCHEMBL28378940 0.90 KDM4E (0.62) KDM4EHSD17B10CDC25ACDC25BTDP1
Acetic Acid SCHEMBL28658551 0.90 KDM4E (0.62) KDM4EHSD17B10CDC25ACDC25BTDP1
Acetic Acid SCHEMBL39490 0.90 KDM4E (0.62) KDM4EHSD17B10CDC25ACDC25BTDP1
Adipic Acid SCHEMBL10713644 0.89 KDM4E (0.53) KDM4EHSD17B10CDC25ACDC25BTDP1
Acetic Acid SCHEMBL17891250 0.88 KDM4E (0.60) KDM4EHSD17B10CDC25ACDC25BTDP1
Succinic Acid SCHEMBL8083562 0.88 KDM4E (0.49) KDM4EHSD17B10CDC25ACDC25BTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024119044-A2 ADRULIPASE COMPOSITIONS First Wave BioPharma, Inc. (US) 2024-06-06 WO claimed
CN-116437947-A Non-pig formulations and methods thereof 第一浪潮生物制药有限公司 2023-07-14 CN claimed
WO-2023114390-A2 LIPASE FORMULATIONS AND METHODS THEREOF First Wave BioPharma, Inc. (US) 2023-06-22 WO claimed
EP-4167970-A1 NON-PORCINE FORMULATIONS AND METHODS THEREOF First Wave Biopharma, Inc. (US) 2023-04-26 EP claimed
EP-3972569-A1 NANOPARTICLES COMPRISING ENZALUTAMIDE Helm AG (DE) 2022-03-30 EP claimed
WO-2021257843-A1 NON-PORCINE FORMULATIONS AND METHODS THEREOF AZURRX BIOPHARMA, INC. (US) 2021-12-23 WO claimed
US-10940117-B2 Oral dosage forms of methyl hydrogen fumarate and prodrugs thereof ARBOR PHARMACEUTICALS, LLC (US) 2021-03-09 US claimed
WO-2020234448-A1 NANOPARTICLES COMPRISING ENZALUTAMIDE HELM AG (DE) 2020-11-26 WO claimed
US-20200246271-A1 ORAL DOSAGE FORMS OF METHYL HYDROGEN FUMARATE AND PRODRUGS THEREOF HPS INVESTMENT PARTNERS, LLC, AS ADMINISTRATIVE AGENT 2020-08-06 US claimed
US-10716760-B2 Oral dosage forms of methyl hydrogen fumarate and prodrugs thereof ARBOR PHARMACEUTICALS, LLC (US) 2020-07-21 US claimed
EP-1239835-A1 PHARMACEUTICAL COMPOSITIONS PROVIDING ENHANCED DRUG CONCENTRATIONS Pfizer Products Inc. (US) 2002-09-18 EP claimed
WO-2002067893-A2 PHARMACEUTICAL FORMULATION COMPRISING BICALUTAMIDE ASTRAZENECA AB (SE) 2002-09-06 WO claimed
US-20020103225-A1 Pharmaceutical compositions of cholesteryl ester transfer protein inhibitors BEND RESEARCH INC. 2002-08-01 US claimed
US-20020006443-A1 Drug in a solubility-improved form with a concentration-enhancing polymer such as hydroxypropyl methyl cellulose acetate succinate; combination improves bioavailability relative to a control of just solubility improved form BEND RESEARCH, INC. 2002-01-17 US claimed
US-20010053791-A1 Glycogen phosphorylase inhibitor BEND RESEARCH, INC. 2001-12-20 US claimed
US-20010053778-A1 Pharmaceutical compositions of glycogen phosphorylase inhibitors BEND RESEARCH, INC. 2001-12-20 US claimed
WO-2001068055-A1 PHARMACEUTICAL COMPOSITIONS OF GLYCOGEN PHOSPHORYLASE INHIBITORS PFIZER PRODUCTS INC. (US) 2001-09-20 WO claimed
WO-2001068092-A2 GLYCOGEN PHOSPHORYLASE INHIBITOR PFIZER PRODUCTS INC. (US) 2001-09-20 WO claimed
WO-2001047495-A1 PHARMACEUTICAL COMPOSITIONS PROVIDING ENHANCED DRUG CONCENTRATIONS PFIZER PRODUCTS INC. (US) 2001-07-05 WO claimed
EP-1027886-A2 Pharmaceutical solid dispersions Pfizer Products Inc. (US) 2000-08-16 EP 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 (6 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-20200246271-A1 ORAL DOSAGE FORMS OF METHYL HYDROGEN FUMARATE AND PRODRUGS THEREOF FH, MGMT, BHMT2 KDM4E 675/4885HSD17B10 488/4885CDC25A 1047/4885
US-20020103225-A1 Pharmaceutical compositions of cholesteryl ester transfer protein inhibitors CETP, HDLBP, NPC1L1 KDM4E 2729/4885HSD17B10 242/4885CDC25A 3846/4885
US-10940117-B2 Oral dosage forms of methyl hydrogen fumarate and prodrugs thereof FH, MGMT, BHMT2 KDM4E 675/4885HSD17B10 488/4885CDC25A 1047/4885
US-20010053791-A1 Glycogen phosphorylase inhibitor PYGL, PYGM, GYS2 KDM4E 2522/4885HSD17B10 261/4885CDC25A 1033/4885
US-20010053778-A1 Pharmaceutical compositions of glycogen phosphorylase inhibitors PYGL, PYGM, GYS2 KDM4E 2299/4885HSD17B10 472/4885CDC25A 849/4885
US-10716760-B2 Oral dosage forms of methyl hydrogen fumarate and prodrugs thereof FH, MGMT, BHMT2 KDM4E 675/4885HSD17B10 488/4885CDC25A 1047/4885

“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.