SCHEMBL63125

SCHEMBL63125

CCC(C)C(NC(=O)CN)C(=O)NC(C(=O)NC(CCC(=O)O)C(=O)NC(CCC(N)=O)C(=O)NC1CSSCC2NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C(CSSCC(NC(=O)C(CC(C)C)NC(=O)C(Cc3cnc[nH]3)NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)Cc3ccccc3)C(C)C)C(=O)NCC(=O)NC(CO)C(=O)NC(Cc3cnc[nH]3)C(=O)NC(CC(C)C)C(=O)NC(C(C)C)C(=O)NC(CCC(=O)O)C(=O)NC(C)C(=O)NC(CC(C)C)C(=O)NC(Cc3ccc(O)cc3)C(=O)NC(CC(C)C)C(=O)NC(C(C)C)C(=O)NC(C(=O)NCC(=O)NC(CCC(=O)O)C(=O)NC(CCCNC(=N)N)C(=O)NCC(=O)NC(Cc3ccccc3)C(=O)NC(Cc3ccccc3)C(=O)NC(Cc3ccc(O)cc3)C(=O)NC(C(=O)N3CCCC3C(=O)NC(CCCCN)C(=O)NC(C(=O)O)C(C)O)C(C)O)CSSCC(C(=O)NC(CC(N)=O)C(=O)O)NC(=O)C(Cc3ccc(O)cc3)NC(=O)C(CC(N)=O)NC(=O)C(CCC(=O)O)NC(=O)C(CC(C)C)NC(=O)C(CCC(N)=O)NC(=O)C(Cc3ccc(O)cc3)NC(=O)C(CC(C)C)NC(=O)C(CO)NC2=O)NC1=O)C(C)C

nearest known ligand 0.98

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
INSR P06213 1/20 0.98
RXFP1 Q9HBX9 1/20 0.69
NPY2R P49146 12/20 0.67
MC4R P32245 1/20 0.65
MC1R Q01726 1/20 0.65
KCNMA1 Q12791 1/20 0.63
KCNMB4 Q86W47 1/20 0.63
CSNK2A2 P19784 1/20 0.62
CSNK2B P67870 1/20 0.62
CSNK2A1 P68400 1/20 0.62
CSNK2A3 Q8NEV1 1/20 0.62
RXFP4 Q8TDU9 3/20 0.61
RXFP3 Q9NSD7 3/20 0.61

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
SCHEMBL15669703 0.98 INSR (0.95) INSRRXFP1NPY2RMC4RMC1R
SCHEMBL14840198 0.97 INSR (0.93) INSRRXFP1NPY2RMC4RMC1R
Insulin Detemir SCHEMBL29350489 0.91 INSR (0.82) INSRRXFP1NPY2RMC4RMC1R
SCHEMBL33618 0.87 INSR (0.75) INSRRXFP1NPY2RMC4RMC1R
SCHEMBL29385832 0.82 MC4R (0.72) INSRRXFP1NPY2RMC4RMC1R
Davalintide SCHEMBL29533482 0.81 RAMP1 (0.77) INSRNPY2R
Calcitonin Salmon SCHEMBL269785 0.80 INSR (0.64) INSRNPY2R
Amylin SCHEMBL29351499 0.80 RAMP1 (0.75) INSRRXFP1NPY2RKCNMA1KCNMB4
Calcitonin Salmon SCHEMBL29392873 0.80 INSR (0.64) INSRNPY2R
SCHEMBL29367000 0.79 NPY2R (0.68) INSRNPY2R

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240238382-A1 URI Agonist/Vasodilator LILLY CO ELI (US) 2024-07-18 US disclosed
CN-115894720-B Long-acting insulin-Fc fusion protein 中国科学院上海药物研究所 2024-07-09 CN disclosed
US-20240207365-A1 METHODS FOR PRODUCING STABLE THERAPEUTIC FORMULATIONS IN APROTIC POLAR SOLVENTS XERIS PHARMACEUTICALS, INC. (US) 2024-06-27 US disclosed
WO-2024110516-A1 TOLEROGENIC COMPOSITION AHEAD THERAPEUTICS, S.L. (ES) 2024-05-30 WO disclosed
WO-2024045890-A1 PREPARATION METHOD FOR DENDRITIC CELL PROGENITORS AND CULTURE MEDIUM THEREOF 浙江吉量科技有限公司 2024-03-07 WO disclosed
CN-117625531-A Preparation method of dendritic cell progenitor cells and culture medium thereof 浙江吉量科技有限公司 2024-03-01 CN disclosed
EP-4327804-A2 METHODS FOR PRODUCING STABLE THERAPEUTIC GLUCAGON FORMULATIONS IN APROTIC POLAR SOLVENTS Xeris Pharmaceuticals, Inc. (US) 2024-02-28 EP disclosed
WO-2024035929-A2 INSULIN SENSITIZERS FOR REVERSAL OF INSULIN RESISTANCE THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-02-15 WO disclosed
US-20240041984-A1 METHODS FOR PRODUCING STABLE THERAPEUTIC FORMULATIONS IN APROTIC POLAR SOLVENTS XERIS PHARMACEUTICALS, INC. (US) 2024-02-08 US disclosed
US-11872266-B2 Rapid-acting insulin compositions ELI LILLY AND COMPANY (US) 2024-01-16 US disclosed
WO-2014138682-A1 COMPOSITIONS AND METHODS FOR CARDIAC TISSUE REPAIR UNIVERSITY OF VERMONT AND STATE AGRICULTURE COLLEGE (US) 2014-09-12 WO disclosed
WO-2014068007-A1 COMPOSITIONS, METHODS AND USES FOR THE TREATMENT OF DIABETES AND RELATED CONDITIONS BY CONTROLLING BLOOD GLUCOSE LEVEL PHARNEXT (FR) 2014-05-08 WO disclosed
US-8129562-B2 Carboxylic acid derivatives DSM IP ASSETS B.V. (NL) 2012-03-06 US disclosed
US-20110136241-A1 TYPE II DIABETES MOLECULAR BIOPROFILE AND METHOD AND SYSTEM OF USING THE SAME NAYLOR STEPHEN 2011-06-09 US disclosed
US-20110124726-A1 NOVEL CARBOXYLIC ACID DERIVATIVES DSM IP ASSETS B.V. 2011-05-26 US disclosed
US-7906496-B2 Carboxylic acid derivatives DSM IP ASSETS B.V. (NL) 2011-03-15 US disclosed
US-20090258887-A1 Novel Carboxylic Acid Derivatives DSM ASSETS B.V. (NL) 2009-10-15 US disclosed
CN-101268039-A Novel carboxylic acid derivatives DSM IP ASSETS BV (NL) 2008-09-17 CN disclosed
EP-1926703-A1 NOVEL CARBOXYLIC ACID DERIVATIVES DSM IP Assets B.V. (NL) 2008-06-04 EP disclosed
WO-2007039059-A1 NOVEL CARBOXYLIC ACID DERIVATIVES DSM IP ASSETS B.V. (NL) 2007-04-12 WO 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 (3 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-20240238382-A1 URI Agonist/Vasodilator GPR119, INSR, IAPP INSR 2/4885RXFP1 35/4885NPY2R 147/4885
US-20090258887-A1 Novel Carboxylic Acid Derivatives AADAC, ALDH7A1, DDC INSR 2289/4885RXFP1 4773/4885NPY2R 4444/4885
US-20110124726-A1 NOVEL CARBOXYLIC ACID DERIVATIVES AADAC, ALDH7A1, ALDH18A1 INSR 2160/4885RXFP1 4719/4885NPY2R 4343/4885

“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.