Succinic Acid

Succinic Acid

SCHEMBL508686

Clc1ccc2c(c1SCc1cnc(NCC3CCCCC3)s1)CCNCC2.O=C(O)CCC(=O)O

nearest known ligand 0.36

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
CDK4 known ✓ P11802 1/20 0.31
CDK2 P24941 5/20 0.36
NPC1 O15118 4/20 0.33
RAB9A P51151 4/20 0.33
SMN1; SMN2 Q16637 3/20 0.33
LMNA P02545 1/20 0.33
CRHR1 P34998 1/20 0.32
HTR2B P41595 1/20 0.32
KDM4C Q9H3R0 2/20 0.32
CNR1 P21554 1/20 0.32
CNR2 P34972 1/20 0.32
ASPH Q12797 2/20 0.32
KDM8 Q8N371 2/20 0.32
KDM4E B2RXH2 1/20 0.32
RIOX2 Q8IUF8 1/20 0.32
CCNE2 O96020 3/20 0.31
CCNE1 P24864 3/20 0.31
CCNB2 O95067 1/20 0.31
CDK1 P06493 1/20 0.31
CCNB1 P14635 1/20 0.31

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
SCHEMBL10230285 0.93 CDK2 (0.40) CDK2NPC1RAB9ASMN1; SMN2LMNA
Succinic Acid SCHEMBL508666 0.83 TPH1 (0.36) CRHR1HTR2BKDM4CASPHKDM8
Succinic Acid SCHEMBL2253730 0.80 CDK2 (0.44) CDK2CRHR1HTR2BCCNE2CCNE1
Succinic Acid SCHEMBL508414 0.76 HCAR3 (0.37) HTR2B
SCHEMBL10230402 0.75 CCNT1 (0.36) CRHR1HTR2BKDM4E
Succinic Acid SCHEMBL507467 0.75 HTR2A (0.37) HTR2B
Succinic Acid SCHEMBL508006 0.74 KDM4E (0.35) SMN1; SMN2HTR2BKDM4EL3MBTL1
Succinic Acid SCHEMBL2252995 0.74 ALDH1A1 (0.42) RAB9ALMNAHTR2BL3MBTL1
SCHEMBL10274857 0.74 HDAC6 (0.41) NPC1RAB9ASMN1; SMN2
Hydrochloric Acid SCHEMBL506710 0.73 HDAC6 (0.40) NPC1RAB9ASMN1; SMN2

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8580780-B2 6 substituted 2, 3,4,5 tetrahydro-1H-benzo[d]azepines as 5-HT2C receptor agonist ELI LILLY AND COMPANY (US) 2013-11-12 US disclosed
EP-2479168-A1 6-Substituted 2,3,4,5-Tetrahydro-1H-Benzo [d]Azepines as 5-HT2C Receptor Agonists ELI LILLY AND COMPANY (US) 2012-07-25 EP disclosed
US-20120028961-A1 6 Substituted 2, 3,4,5 Tetrahydro-1H-Benzo[d]Azepines as 5-HT2c Receptor Agonist ELI LILLY AND COMPANY (US) 2012-02-02 US disclosed
US-8022062-B2 6-substituted 2,3,4,5-tetrahydro-1H-benzo[d]azepines as 5-HT2C receptor agonists ELI LILLY AND COMPANY (US) 2011-09-20 US disclosed
US-20090099155-A1 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPINES AS 5-HT2C RECEPTOR AGONISTS ARRAY BIOPHARMA, INC. 2009-04-16 US disclosed

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-20090099155-A1 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPINES AS 5-HT2C RECEPTOR AGONISTS HTR2C, HTR5A, HTR4 CDK4 1811/4885CDK2 1698/4885NPC1 2664/4885
US-20120028961-A1 6 Substituted 2, 3,4,5 Tetrahydro-1H-Benzo[d]Azepines as 5-HT2c Receptor Agonist HTR2C, HTR4, HTR1A CDK4 1421/4885CDK2 1960/4885NPC1 3189/4885

“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.