SCHEMBL7330813

SCHEMBL7330813

CN1CCN(S(=O)(=O)C[C@@H](Cc2ccccc2)C(=O)O)CC1

nearest known ligand 0.50

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 1/20 0.50
CYP1A2 P05177 1/20 0.50
CHRM1 P11229 3/20 0.49
IDO1 P14902 1/20 0.46
CPA3 P15088 3/20 0.45
CPA1 P15085 2/20 0.45
FOLH1 Q04609 1/20 0.45
CPB1 P15086 1/20 0.45
CPB2 Q96IY4 1/20 0.45
CTSS P25774 1/20 0.45
POLB P06746 1/20 0.44
TSHR P16473 2/20 0.44
ALDH1A1 P00352 1/20 0.44
GAA P10253 1/20 0.43
CYP2C19 P33261 1/20 0.43
KMT2A Q03164 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43

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
SCHEMBL7338169 1.00 HSD17B10 (0.50) HSD17B10CYP1A2CHRM1IDO1CPA3
SCHEMBL7333389 0.87 CYP1A2 (0.54) CYP1A2CPA3CPA1FOLH1CPB1
SCHEMBL7332863 0.87 HSD17B10 (0.46) HSD17B10CHRM1IDO1CTSSPOLB
SCHEMBL7301756 0.84 LMNA (0.56) CYP1A2CPA3CPA1FOLH1CPB1
SCHEMBL8909332 0.84 LMNA (0.56) CYP1A2CPA3CPA1FOLH1CPB1
SCHEMBL7353235 0.81 REN (0.47) HSD17B10CTSS
SCHEMBL7330013 0.81 CYP1A2 (0.44) CYP1A2CPA3CPA1FOLH1CPB1
SCHEMBL7336528 0.81 TSHR (0.50) TSHRALDH1A1GAACYP2C19
SCHEMBL7148417 0.80 POLB (0.55) POLBTSHRALDH1A1KMT2A
SCHEMBL9437516 0.80 REN (0.38) HSD17B10CHRM1IDO1CTSSPOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0456185-B1 Renin inhibitors ABBOTT LAB (US) 1995-05-31 EP claimed
EP-0655063-B1 ETHYNYL ALANINE AMINO DIOL COMPOUNDS HAVING A PIPERAZINYL-TERMINATED GROUP OR A PIPERAZINYL-ALKYLAMINO-TERMINATED GROUP FOR TREATMENT OF HYPERTENSION SEARLE & CO (US) 1999-09-22 EP disclosed
US-5523289-A RENIN INHIBITOR ABBOTT LABORATORIES (US) 1996-06-04 US disclosed
EP-0456185-B1 Renin inhibitors ABBOTT LAB (US) 1995-05-31 EP disclosed
US-5344990-A Process for the preparation of a renin inhibiting compound ABBOTT LABORATORIES (US) 1994-09-06 US disclosed
US-5332742-A Ocular hypotensive ABBOTT LABORATORIES (US) 1994-07-26 US disclosed
US-5310740-A Congestive heart failure, hypotensive agents, antiglaucoma agents; side effect reduction ABBOTT LABORATORIES (US) 1994-05-10 US disclosed
US-5298505-A Ethynyl alanine amino diol compounds having a piperazinyl-terminated group or a piperazinyl-alkylamino-terminated group for treatment of hypertension G. D. SEARLE & CO. (US) 1994-03-29 US disclosed
WO-1994004536-A1 ETHYNYL ALANINE AMINO DIOL COMPOUNDS HAVING A PIPERAZINYL-TERMINATED GROUP OR A PIPERAZINYL-ALKYLAMINO-TERMINATED GROUP FOR TREATMENT OF HYPERTENSION G.D. SEARLE & CO. (US) 1994-03-03 WO disclosed
US-5284849-A Treating hypertension and congestive heart failure ABBOTT LABORATORIES (US) 1994-02-08 US disclosed
US-5275950-A Process for the preparation of a renin inhibiting compound ABBOTT LABORATORIES (US) 1994-01-04 US disclosed
US-5258362-A Enzyme inhibitors, amides with oxetane ring ABBOTT LABORATORIES (US) 1993-11-02 US disclosed
WO-1993007886-A1 PHARMACEUTICAL COMPOSITION CONTAINING CERTAIN PEPTIDOMIMETIC COMPOUNDS ABBOTT LABORATORIES (US) 1993-04-29 WO disclosed
WO-1993002667-A1 PHARMACEUTICAL COMPOSITION ABBOTT LABORATORIES (US) 1993-02-18 WO disclosed
US-5182266-A Method for treating renal disease ABBOTT LABORATORIES (US) 1993-01-26 US disclosed
US-5178877-A Cardiovascular disorders ABBOTT LABORATORIES (US) 1993-01-12 US disclosed
US-5122514-A Administering renin inhibitor ABBOTT LABORATORIES (US) 1992-06-16 US disclosed
EP-0456185-A2 Renin inhibitors ABBOTT LABORATORIES (US) 1991-11-13 EP disclosed
WO-1991016031-A1 PSORIASIS TREATMENT ABBOTT LABORATORIES (US) 1991-10-31 WO disclosed