Cyclopropanecarboxylic Acid Amide

Cyclopropanecarboxylic Acid Amide

SCHEMBL3255991

CC(=O)O.NC(=O)C1CC1

nearest known ligand 0.48

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Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Cyclopropanecarboxylic Acid Amide. 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
NOS2 known ✓ P35228 1/20 0.36
SMN1; SMN2 Q16637 3/20 0.48
GAA P10253 1/20 0.42
FFAR3 O14843 1/20 0.41
LCK P06239 1/20 0.41
FYN P06241 1/20 0.41
KDM4E B2RXH2 2/20 0.39
MAPT P10636 1/20 0.39
KMT2A Q03164 1/20 0.39
ATM Q13315 1/20 0.39
CYP2D6 P10635 1/20 0.39
LMNA P02545 2/20 0.39
ALOX15 P16050 1/20 0.39
BLM P54132 1/20 0.39
PMP22 Q01453 1/20 0.39
ALDH1A1 P00352 2/20 0.37
PLG P00747 1/20 0.37
PLAT P00750 1/20 0.37
EPHX1 P07099 1/20 0.37
TSHR P16473 1/20 0.36

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
Cyclopropanecarboxylic Acid Amide SCHEMBL8743189 0.88 SMN1; SMN2 (0.46) SMN1; SMN2GAAKDM4EMAPTKMT2A
SCHEMBL383436 0.87 SMN1; SMN2 (0.50) SMN1; SMN2GAAKDM4EMAPTKMT2A
SCHEMBL13332956 0.87 SMN1; SMN2 (0.50) SMN1; SMN2GAAKDM4EMAPTKMT2A
Cyclopropanecarboxylic Acid Amide SCHEMBL6927157 0.87 SMN1; SMN2 (0.50) SMN1; SMN2GAAKDM4EMAPTKMT2A
SCHEMBL9797557 0.87 SMN1; SMN2 (0.50) SMN1; SMN2GAAKDM4EMAPTKMT2A
SCHEMBL28418543 0.87 SMN1; SMN2 (0.50) SMN1; SMN2GAAKDM4EMAPTKMT2A
Cyclopropanecarboxylic Acid Amide SCHEMBL5661 0.87
SCHEMBL12513456 0.86 SMN1; SMN2 (0.46) SMN1; SMN2GAAKDM4EMAPTKMT2A
SCHEMBL12437076 0.86 SMN1; SMN2 (0.46) SMN1; SMN2GAAKDM4EMAPTKMT2A
Cyclopropanecarboxylic Acid Amide SCHEMBL29183025 0.85 KDM4E (0.46) SMN1; SMN2GAAKDM4EMAPTKMT2A

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
CN-107406447-A The crystal form of pyrrolopyridine compounds 基因泰克公司 2017-11-28 CN disclosed
WO-2010011584-A2 PROCESS FOR MAKING A RENIN INHIBITOR MERCK & CO., INC. (US) 2010-01-28 WO disclosed
EP-1385524-A4 PYRAZOLOPYRIMIDINES AS THERAPEUTIC AGENTS ABBOTT GMBH & CO KG (DE) 2006-02-01 EP disclosed
EP-1385524-A1 PYRAZOLOPYRIMIDINES AS THERAPEUTIC AGENTS Abbott GmbH & Co. KG (DE) 2004-02-04 EP disclosed
WO-2002080926-A1 PYRAZOLOPYRIMIDINES AS THERAPEUTIC AGENTS ABBOTT GMBH & CO. KG (DE) 2002-10-17 WO disclosed