Gabapentin

Gabapentin

SCHEMBL2862353

NCC1(CC(=O)O)CCCCC1.c1ccccc1

nearest known ligand 0.92

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8

The experimentally established mechanism targets of Gabapentin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CACNA2D1 known ✓ P54289 1/20 0.92
ALDH1A1 P00352 5/20 0.92
USP2 O75604 2/20 0.92
CYP1A2 P05177 2/20 0.92
LMNA P02545 1/20 0.92
TSHR P16473 1/20 0.92
BLM P54132 1/20 0.92
SMN1; SMN2 Q16637 1/20 0.92
CYP2C19 P33261 1/20 0.47
GAA P10253 1/20 0.46
MAPK1 P28482 1/20 0.45
HPGD P15428 1/20 0.44
KMT2A Q03164 1/20 0.42
KDM4E B2RXH2 1/20 0.41
MAPT P10636 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
SCHEMBL6544499 0.96 CYP1A2 (1.00) ALDH1A1USP2CYP1A2LMNATSHR
Gabapentin SCHEMBL4030100 0.96 CYP1A2 (1.00) ALDH1A1USP2CYP1A2LMNATSHR
Gabapentin SCHEMBL8343 0.96 CYP1A2 (1.00) ALDH1A1USP2CYP1A2LMNATSHR
SCHEMBL466183 0.96 CYP1A2 (1.00) ALDH1A1USP2CYP1A2LMNATSHR
Gabapentin SCHEMBL179836 0.96 CYP1A2 (1.00) ALDH1A1USP2CYP1A2LMNATSHR
Gabapentin SCHEMBL19031792 0.94 CYP1A2 (0.96) ALDH1A1USP2CYP1A2LMNATSHR
Gabapentin SCHEMBL6689206 0.94 CYP1A2 (0.96) ALDH1A1USP2CYP1A2LMNATSHR
Gabapentin SCHEMBL6672099 0.94 CYP1A2 (0.96) ALDH1A1USP2CYP1A2LMNATSHR
Gabapentin SCHEMBL26730 0.94 CYP1A2 (0.96) ALDH1A1USP2CYP1A2LMNATSHR
Gabapentin SCHEMBL5050957 0.94 CYP1A2 (0.96) ALDH1A1USP2CYP1A2LMNATSHR

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
EP-1603863-B1 PROCESS FOR THE PREPARATION OF AMINO METHYL CYCLO ALKANE ACETIC ACIDS HIKAL LTD (IN) 2010-01-13 EP disclosed
US-7635717-B2 Process for the preparation of amino methyl cyclo alkane acetic acids HIKAL LIMITED (IN) 2009-12-22 US disclosed
US-20060149099-A1 Process for the preparation of amino methyl cyclo alkane acetic acids HIKAL LIMITED 2006-07-06 US disclosed
EP-1603863-A1 PROCESS FOR THE PREPARATION OF AMINO METHYL CYCLO ALKANE ACETIC ACIDS Hikal Ltd. (IN) 2005-12-14 EP disclosed
WO-2004046085-A1 PROCESS FOR THE PREPARATION OF AMINO METHYL CYCLO ALKANE ACETIC ACIDS HIKAL LTD. (IN) 2004-06-03 WO 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 (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-20060149099-A1 Process for the preparation of amino methyl cyclo alkane acetic acids GABRA1, GABRA6, ACMSD CACNA2D1 261/4885ALDH1A1 366/4885USP2 1057/4885

“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.