SCHEMBL1682664

SCHEMBL1682664

O=C(Cn1ncnn1)c1ccccc1Cl

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ POLB P06746 2/20 0.58
▸ ALDH1A1 P00352 3/20 0.49
▸ MAPT P10636 2/20 0.49
▸ RAB9A P51151 5/20 0.45
▸ SMN1; SMN2 Q16637 2/20 0.45
▸ ERCC5 P28715 1/20 0.44
▸ FEN1 P39748 1/20 0.44
▸ CXCR3 P49682 1/20 0.44
▸ HSP90AA1 P07900 1/20 0.43
▸ PAX8 Q06710 1/20 0.43
▸ NPC1 O15118 2/20 0.42
▸ MGAM O43451 1/20 0.42
▸ AMY1A P0DUB6 1/20 0.42
▸ GAA P10253 1/20 0.42
▸ SI P14410 1/20 0.42
▸ MGAM2 Q2M2H8 1/20 0.42
▸ CES2 O00748 1/20 0.42
▸ CES1 P23141 1/20 0.42
▸ KMT2A Q03164 3/20 0.41
▸ MEN1 O00255 2/20 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
SCHEMBL30356468 1.00 POLB (0.58) POLBALDH1A1MAPTRAB9ASMN1; SMN2
SCHEMBL30356525 0.85 POLB (0.46) POLBALDH1A1MAPTRAB9ASMN1; SMN2
SCHEMBL6558564 0.84 ALDH1A1 (0.53) POLBALDH1A1MAPTRAB9ASMN1; SMN2
SCHEMBL29025711 0.81 POLB (0.45) POLBALDH1A1ERCC5FEN1PLAU
SCHEMBL29025637 0.80 POLB (0.46) POLBALDH1A1MAPTSMN1; SMN2KMT2A
SCHEMBL30356535 0.80 POLB (0.46) POLBALDH1A1MAPTSMN1; SMN2KMT2A
SCHEMBL29025627 0.75 POLB (0.42) POLBALDH1A1MAPTHSP90AA1PLAU
SCHEMBL30356530 0.75 POLB (0.42) POLBALDH1A1MAPTHSP90AA1PLAU
SCHEMBL21821207 0.74 PLAU (0.51) POLBALDH1A1RAB9ASMN1; SMN2GAA
SCHEMBL30817843 0.73 HMOX1 (0.50) POLBALDH1A1MAPTRAB9ASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116143717-B Deuterated carbamate compound and application thereof in medicine 康百达(四川)生物医药科技有限公司 2025-05-06 — — CN disclosed
CN-115974799-B Carbamate substituted alcohol derivative and application thereof in medicine 成都百裕制药股份有限公司 2024-08-13 — — CN disclosed
CN-117736157-A Preparation method of tetrazole-substituted acetophenone compound 江苏恩华药业股份有限公司 2024-03-22 — — CN disclosed
WO-2023152711-A1 PROCESS FOR THE PREPARATION OF CENOBAMATE AND INTERMEDIATES THEREOF METROCHEM API PVT LTD (IN) 2023-08-17 — — WO disclosed
CN-116143717-A Deuterated carbamate compound and application thereof in medicine 成都百裕制药股份有限公司 2023-05-23 — — CN disclosed
CN-115974799-A Carbamate substituted alcohol derivatives and their use in medicine 成都百裕制药股份有限公司 2023-04-18 — — CN disclosed
US-9434970-B2 Method for preparation of carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester SK BIOPHARMACEUTICALS CO., LTD. (KR) 2016-09-06 — — US disclosed
US-20150252398-A1 METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER SK BIOPHARMACEUTICALS CO LTD (KR) 2015-09-10 — — US disclosed
US-9068207-B2 Method for preparation of carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester SK BIOPHARMACEUTICALS CO. LTD. (KR) 2015-06-30 — — US disclosed
EP-2445890-B1 METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER SK BIOPHARMACEUTICALS CO LTD (KR) 2015-05-06 — — EP disclosed
EP-2488505-B1 METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER SK BIOPHARMACEUTICALS CO LTD (KR) 2015-02-25 — — EP disclosed
US-20140073018-A1 Method for Preparation of Carbamic Acid (R)-1-Aryl-2 Tetrazolyl-Ethyl Ester SK BIOPHARMACEUTICALS CO. LTD. (KR) 2014-03-13 — — US disclosed
US-8501436-B2 Method for preparation of carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester SK BIOPHARMACEUTICALS CO. LTD. (KR) 2013-08-06 — — US disclosed
US-8404461-B2 Method for preparation of carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester SK Biopharmaceutical Co. Ltd. (KR) 2013-03-26 — — US disclosed
EP-2488505-A2 METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER SK Biopharmaceuticals Co., Ltd. (KR) 2012-08-22 — — EP disclosed
EP-2445890-A1 METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER SK Biopharmaceuticals Co., Ltd. (KR) 2012-05-02 — — EP disclosed
US-20110111467-A1 Method for Preparation of Carbamic Acid (R)-1-Aryl-2-Tetrazolyl-Ethyl Ester SK BIOPHARMACEUTICALS CO. LTD. (KR) 2011-05-12 — — US disclosed
WO-2011046380-A2 METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER SK HOLDINGS CO.,LTD. (KR) 2011-04-21 — — WO disclosed
WO-2010150946-A1 METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER SK HOLDINGS CO., LTD. (KR) 2010-12-29 — — WO disclosed
US-20100323410-A1 METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER SK BIOPHARMACEUTICALS CO. LTD. (KR) 2010-12-23 — — 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-20110111467-A1 Method for Preparation of Carbamic Acid (R)-1-Aryl-2-Tetrazolyl-Ethyl Ester CES1, ADH1A, ADH1C POLB 2925/4885ALDH1A1 46/4885MAPT 3707/4885
US-20100323410-A1 METHOD FOR PREPARATION OF CARBAMIC ACID (R)-1-ARYL-2-TETRAZOLYL-ETHYL ESTER CPS1, ADH1A, KHK POLB 3659/4885ALDH1A1 161/4885MAPT 3770/4885

“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.

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