SCHEMBL279916

SCHEMBL279916

C[C@@H](CCCC(=O)O)C(=O)O

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.73
BLM P54132 1/20 0.56
LTA4H P09960 1/20 0.55
GABRR1 P24046 2/20 0.52
LMNA P02545 2/20 0.48
SLC22A6 Q4U2R8 1/20 0.48
FFAR4 Q5NUL3 1/20 0.47
ACE2 Q9BYF1 1/20 0.47
FFAR1 O14842 1/20 0.47
GABRP O00591 2/20 0.46
GABRD O14764 2/20 0.46
GABRA1 P14867 2/20 0.46
GABRB1 P18505 2/20 0.46
GABRG2 P18507 2/20 0.46
GABRB3 P28472 2/20 0.46
GABRA5 P31644 2/20 0.46
GABRA3 P34903 2/20 0.46
GABRA2 P47869 2/20 0.46
GABRB2 P47870 2/20 0.46
GABRA4 P48169 2/20 0.46

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
SCHEMBL18317937 1.00 CYP1A2 (0.73) CYP1A2BLMLTA4HGABRR1LMNA
SCHEMBL148481 1.00 CYP1A2 (0.73) CYP1A2BLMLTA4HGABRR1LMNA
SCHEMBL11470798 0.98 CYP1A2 (0.70) CYP1A2BLMLTA4HGABRR1LMNA
SCHEMBL7926923 0.98 CYP1A2 (0.70) CYP1A2BLMLTA4HGABRR1LMNA
Adipic Acid SCHEMBL11140296 0.98 CYP1A2 (0.70) CYP1A2BLMLTA4HGABRR1LMNA
Hydrochloric Acid SCHEMBL10654637 0.98 CYP1A2 (0.70) CYP1A2BLMLTA4HGABRR1LMNA
SCHEMBL11453210 0.98 CYP1A2 (0.70) CYP1A2BLMLTA4HGABRR1LMNA
Ethane SCHEMBL14360148 0.98 CYP1A2 (0.70) CYP1A2BLMLTA4HGABRR1LMNA
Hydrochloric Acid SCHEMBL11815233 0.98 CYP1A2 (0.70) CYP1A2BLMLTA4HGABRR1LMNA
Pimelic Acid SCHEMBL8471838 0.95 CYP1A2 (0.67) CYP1A2BLMLTA4HLMNASLC22A6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8133704-B2 Biological synthesis of difunctional alkanes from carbohydrate feedstocks CELEXION, LLC (US) 2012-03-13 US disclosed
US-20110171696-A1 Biological Synthesis of Difunctional Alkanes from Carbohydrate Feedstocks CELEXION, LLC (US) 2011-07-14 US disclosed
EP-0202069-A2 Process for preparation of biaxially drawn laminated films MITSUBISHI KASEI POLYTEC COMPANY (JP) 1986-11-20 EP disclosed