SCHEMBL10923948

SCHEMBL10923948

NCCc1cn(F)c2ccccc12

nearest known ligand 0.64

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 1/20 0.64
HTR6 P50406 15/20 0.53
SCN9A Q15858 1/20 0.50
TAAR1 Q96RJ0 2/20 0.44
OPRM1 P35372 1/20 0.41
OPRK1 P41145 1/20 0.41
OPRL1 P41146 1/20 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
SCHEMBL7561915 0.79 HTR2A (0.66) HTR2AHTR6SCN9ATAAR1
SCHEMBL5738832 0.79 POLB (0.59) HTR2A
SCHEMBL28806593 0.79 POLB (0.41) HTR2AHTR6
SCHEMBL332959 0.78 HTR2A (1.00) HTR2AHTR6SCN9A
SCHEMBL6787250 0.78 HTR2A (0.64) HTR2AHTR6SCN9ATAAR1
SCHEMBL25166949 0.78 HTR2A (0.64) HTR2AHTR6SCN9ATAAR1OPRM1
SCHEMBL106451 0.78 HTR2A (0.64) HTR2AHTR6SCN9ATAAR1OPRM1
SCHEMBL8374898 0.77 HTR2A (0.58) HTR2AHTR6SCN9ATAAR1OPRM1
Hydrochloric Acid SCHEMBL9695585 0.76 HTR2A (0.62) HTR2AHTR6SCN9ATAAR1OPRM1
Ammonia Solution, Strong SCHEMBL28037069 0.76 HTR2A (0.62) HTR2AHTR6SCN9ATAAR1OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4428880-A Azepino[4,5-d]indole derivatives and preparation thereof S.A. OMNICHEM (BE) 1984-01-31 US claimed
US-20250354108-A1 METHODS FOR PRODUCING MONOTERPENE INDOLE ALKALOIDS UNIV DANMARKS TEKNISKE (DK) 2025-11-20 US disclosed
EP-4526426-A2 METHODS FOR PRODUCING MONOTERPENE INDOLE ALKALOIDS Danmarks Tekniske Universitet (DK) 2025-03-26 EP disclosed
US-20240417764-A1 METHODS FOR THE PRODUCTION OF TRYPTOPHANS, TRYPTAMINES, INTERMEDIATES, SIDE PRODUCTS AND DERIVATIVES MIAMI UNIVERSITY 2024-12-19 US disclosed
EP-4426676-A2 METHODS FOR THE PRODUCTION OF TRYPTOPHANS, TRYPTAMINES, INTERMEDIATES, SIDE PRODUCTS AND DERIVATIVES MIAMI UNIVERSITY (US) 2024-09-11 EP disclosed
WO-2023081837-A9 METHODS FOR THE PRODUCTION OF TRYPTOPHANS, TRYPTAMINES, INTERMEDIATES, SIDE PRODUCTS AND DERIVATIVES MIAMI UNIVERSITY (US) 2024-03-14 WO disclosed
WO-2023222879-A2 METHODS FOR PRODUCING MONOTERPENE INDOLE ALKALOIDS DANMARKS TEKNISKE UNIVERSITET (DK) 2023-11-23 WO disclosed
WO-2023081837-A2 METHODS FOR THE PRODUCTION OF TRYPTOPHANS, TRYPTAMINES, INTERMEDIATES, SIDE PRODUCTS AND DERIVATIVES MIAMI UNIVERSITY (US) 2023-05-11 WO disclosed
US-20210353763-A1 SITE-SPECIFIC COVALENT CHEMICAL LIGATION TO MONOCLONAL AND POLYCLONAL IMMUNOGLOBULIN THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2021-11-18 US disclosed
US-10588982-B2 Site-specific covalent chemical ligation to monoclonal and polyclonal immunoglobulin THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2020-03-17 US disclosed
WO-2016164843-A1 SITE-SPECIFIC COVALENT CHEMICAL LIGATION TO MONOCLONAL AND POLYCLONAL IMMUNOGLOBULIN Lac Diana (US) 2016-10-13 WO disclosed
CN-102014897-B Compound, compositions and its preparation method SIGNUM BIOSCIENCES, INC. (US) 2015-08-05 CN disclosed
US-20140199316-A1 METHODS OF TREATING COMPLICATIONS AND DISORDERS ASSOCIATED WITH G-CSF ADMINISTRATION SACKSTEIN ROBERT (US) 2014-07-17 US disclosed
US-8765126-B2 Methods of treating complications and disorders associated with G-CSF administration SACKSTEIN ROBERT (US) 2014-07-01 US disclosed
US-20130224217-A1 METHODS OF TREATING COMPLICATIONS AND DISORDERS ASSOCIATED WITH G-CSF ADMINISTRATION SACKSTEIN ROBERT (US) 2013-08-29 US disclosed
WO-2012151576-A1 METHODS OF TREATING COMPLICATIONS AND DISORDERS ASSOCIATED WITH G-CSF ADMINISTRATION SACKSTEIN ROBERT (US) 2012-11-08 WO disclosed
EP-0064317-B1 PYRROLO(2,3-D)CARBAZOLE DERIVATIVES, PREPARATION THEREOF AND THEIR THERAPEUTICAL USE OMNICHEM Société anonyme (BE) 1986-02-26 EP disclosed
US-4428880-A Azepino[4,5-d]indole derivatives and preparation thereof S.A. OMNICHEM (BE) 1984-01-31 US disclosed
US-4362739-A Pyrrolo(2,3-d)carbazole derivatives, compositions and use S.A. OMNICHEM (BE) 1982-12-07 US disclosed
EP-0064317-A2 Pyrrolo(2,3-d)carbazole derivatives, preparation thereof and their therapeutical use OMNICHEM Société anonyme (BE) 1982-11-10 EP 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 (5 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-20140199316-A1 METHODS OF TREATING COMPLICATIONS AND DISORDERS ASSOCIATED WITH G-CSF ADMINISTRATION MPO, CSF3R, CSF1R HTR2A 3775/4885HTR6 4477/4885SCN9A 4002/4885
US-20210353763-A1 SITE-SPECIFIC COVALENT CHEMICAL LIGATION TO MONOCLONAL AND POLYCLONAL IMMUNOGLOBULIN FCGR3B, FCGR2A, FCGR1A HTR2A 4084/4885HTR6 4174/4885SCN9A 4031/4885
US-10588982-B2 Site-specific covalent chemical ligation to monoclonal and polyclonal immunoglobulin FCGR3B, FCGR2A, FCGR1A HTR2A 4084/4885HTR6 4174/4885SCN9A 4031/4885
US-20130224217-A1 METHODS OF TREATING COMPLICATIONS AND DISORDERS ASSOCIATED WITH G-CSF ADMINISTRATION MPO, CSF3R, CSF1R HTR2A 3775/4885HTR6 4477/4885SCN9A 4002/4885
US-20250354108-A1 METHODS FOR PRODUCING MONOTERPENE INDOLE ALKALOIDS INMT, KARS1, MIA3 HTR2A 2339/4885HTR6 3067/4885SCN9A 4497/4885

“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.