SCHEMBL85536

SCHEMBL85536

CC(C)(C)OC(=O)N1CCC[C@@H]1C(=O)O

nearest known ligand 0.69

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 2/20 0.69
SMN1; SMN2 Q16637 2/20 0.60
RAB9A P51151 1/20 0.56
LMNA P02545 2/20 0.54
CYP2C19 P33261 1/20 0.54
NPC1 O15118 1/20 0.53
ALDH1A1 P00352 2/20 0.53
NPSR1 Q6W5P4 1/20 0.51
UCHL1 P09936 2/20 0.49
KMT2A Q03164 2/20 0.47
MEN1 O00255 1/20 0.47
POLB P06746 1/20 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
SCHEMBL67044 1.00 HSD17B10 (0.69) HSD17B10SMN1; SMN2RAB9ALMNACYP2C19
SCHEMBL27877016 1.00 HSD17B10 (0.69) HSD17B10SMN1; SMN2RAB9ALMNACYP2C19
SCHEMBL67045 1.00 HSD17B10 (0.69) HSD17B10SMN1; SMN2RAB9ALMNACYP2C19
SCHEMBL6219872 1.00 HSD17B10 (0.69) HSD17B10SMN1; SMN2RAB9ALMNACYP2C19
SCHEMBL20492528 0.98 HSD17B10 (0.68) HSD17B10SMN1; SMN2RAB9ALMNACYP2C19
Ammonia Solution, Strong SCHEMBL28264574 0.98 HSD17B10 (0.68) HSD17B10SMN1; SMN2RAB9ALMNACYP2C19
Hydrazine SCHEMBL28122430 0.97 HSD17B10 (0.66) HSD17B10SMN1; SMN2RAB9ALMNACYP2C19
SCHEMBL1809663 0.95 HSD17B10 (0.64) HSD17B10SMN1; SMN2RAB9ALMNACYP2C19
SCHEMBL77858 0.95 HSD17B10 (0.63) HSD17B10SMN1; SMN2RAB9ALMNACYP2C19
SCHEMBL65491 0.95 HSD17B10 (0.63) HSD17B10SMN1; SMN2RAB9ALMNACYP2C19

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 1053 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024216095-A1 SYNTHESIS OF MAVORIXAFOR AND INTERMEDIATES THEREOF X4 PHARMACEUTICALS, INC. (US) 2024-10-17 WO claimed
CN-112638871-B (R) -4- (1- (1- (4- (trifluoromethyl) benzyl) pyrrolidine-2-carboxamide) cyclopropyl) benzoic acid as EP4 receptor antagonist 罗达制药生物技术有限责任公司 2024-08-30 CN claimed
CN-116898921-B Preparation method of cattail and dyer woad compound traditional Chinese medicine preparation 江西新世纪民星动物保健品有限公司 2024-05-31 CN claimed
CN-117658830-A Preparation method of trans-2-aminocyclopentanol with high optical purity 大连双硼医药化工有限公司 2024-03-08 CN claimed
WO-2024017221-A1 SYNTHESIS METHOD FOR α-AZIDO KETONE CONTAINING TERTIARY STEREOCENTER 常州大学 2024-01-25 WO claimed
CN-114106050-B Compact chiral environment biphenanthrene skeleton chiral phosphoric acid and preparation method and application thereof 华东理工大学 2024-01-12 CN claimed
CN-116898921-A Preparation method of cattail and dyer woad compound traditional Chinese medicine preparation 江西新世纪民星动物保健品有限公司 2023-10-20 CN claimed
CN-115108937-B Synthesis method of alpha-azido ketone containing three-level stereo center 常州大学 2023-08-22 CN claimed
US-11718582-B2 (R)-4-(1-(1-(4-(trifluoromethyl)benzyl)pyrrolidine-2-carboxamide)cyclopropyl)-benzoic acid as EP4 receptor antagonist ROTTAPHARM BIOTECH S.R.L. (IT) 2023-08-08 US claimed
CN-113773295-B Synthesis method of monosubstituted dihydro chromone and application of monosubstituted dihydro chromone in treatment of pulmonary inflammation such as COPD (chronic disease) 广东省科学院动物研究所 2023-06-20 CN claimed
EP-3820842-B1 (R)-4-(1-(1-(4-(TRIFLUOROMETHYL)BENZYL)PYRROLIDINE-2-CARBOXAMIDE)CYCLOPROPYL)-BENZOIC ACID AS EP4 RECEPTOR ANTAGONIST Rottapharm Biotech Srl (IT) 2023-03-29 EP claimed
CN-115108937-A Synthesis method of alpha-azidoketone containing three-level stereocenter 常州大学 2022-09-27 CN claimed
CN-114106050-A Tight chiral environment biphenyl-phenanthrene framework chiral phosphoric acid and preparation method and application thereof 华东理工大学 2022-03-01 CN claimed
EP-3820842-A1 (R)-4-(1-(1-(4-(TRIFLUOROMETHYL)BENZYL)PYRROLIDINE-2-CARBOXAMIDE)CYCLOPROPYL)-BENZOIC ACID AS EP4 RECEPTOR ANTAGONIST Rottapharm Biotech S.r.l. (IT) 2021-05-19 EP claimed
US-20210130290-A1 (R)-4-(1-(1-(4-(TRIFLUOROMETHYL)BENZYL)PYRROLIDINE-2-CARBOXAMIDE)CYCLOPROPYL)-BENZOIC ACID AS EP4 RECEPTOR ANTAGONIST ROTTAPHARM BIOTECH S.R.L. (IT) 2021-05-06 US claimed
CN-112638871-A (R) -4- (1- (1- (4- (trifluoromethyl) benzyl) pyrrolidine-2-carboxamide) cyclopropyl) benzoic acid as EP4 receptor antagonists 罗达制药生物技术有限责任公司 2021-04-09 CN claimed
WO-2020012305-A1 (R)-4-(1-(1-(4-(TRIFLUOROMETHYL)BENZYL)PYRROLIDINE-2-CARBOXAMIDE)CYCLOPROPYL)-BENZOIC ACID AS EP4 RECEPTOR ANTAGONIST ROTTAPHARM BIOTECH S.R.L. (IT) 2020-01-16 WO claimed
EP-4565562-B1 PYRROLIDINE-2-CARBOXAMIDE DERIVATIVES AS PROSTAGLANDIN E2 RECEPTOR 4 (EP4) AGONISTS FOR THE TREATMENT OF GASTROINTESTINAL AND PULMONARY DISEASES NXERA PHARMA UK LTD (GB) 2026-05-27 EP disclosed
EP-0138407-A1 Azetidinones E.R. Squibb & Sons, Inc. (US) 1985-04-24 EP disclosed
US-4505853-A GLANDULAR DISORDERS ORTHO PHARMACEUTICAL CORPORATION (US) 1985-03-19 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-11718582-B2 (R)-4-(1-(1-(4-(trifluoromethyl)benzyl)pyrrolidine-2-carboxamide)cyclopropyl)-benzoic acid as EP4 receptor antagonist PTGER4, PTGER1, PTGER2 HSD17B10 2486/4885SMN1; SMN2 3641/4885RAB9A 3772/4885
US-20210130290-A1 (R)-4-(1-(1-(4-(TRIFLUOROMETHYL)BENZYL)PYRROLIDINE-2-CARBOXAMIDE)CYCLOPROPYL)-BENZOIC ACID AS EP4 RECEPTOR ANTAGONIST PTGER4, PTGER1, PTGER2 HSD17B10 2486/4885SMN1; SMN2 3641/4885RAB9A 3772/4885

“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.