Iproheptine

Iproheptine

SCHEMBL616269

CC(C)CCCC(C)NC(C)C.Cl

nearest known ligand 0.43

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Iproheptine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.43
TDP1 Q9NUW8 1/20 0.35
MEN1 O00255 1/20 0.34
ALDH1A1 P00352 1/20 0.34
HTT P42858 1/20 0.34
KMT2A Q03164 1/20 0.34
APEX1 P27695 1/20 0.33
PMP22 Q01453 1/20 0.33
BLM P54132 1/20 0.32
CYP1A2 P05177 1/20 0.30
CYP2D6 P10635 1/20 0.30

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
Iproheptine SCHEMBL23902081 0.97 LMNA (0.46) LMNATDP1MEN1ALDH1A1HTT
Iproheptine SCHEMBL48719 0.97 LMNA (0.46) LMNATDP1MEN1ALDH1A1HTT
Iproheptine SCHEMBL18541892 0.97 LMNA (0.46) LMNATDP1MEN1ALDH1A1HTT
SCHEMBL277041 0.86 LMNA (0.50) LMNAMEN1ALDH1A1HTTKMT2A
SCHEMBL19080590 0.80 TDP1 (0.41) LMNATDP1ALDH1A1APEX1PMP22
Hydrochloric Acid SCHEMBL11540172 0.77 TDP1 (0.33) TDP1APEX1PMP22
SCHEMBL17198262 0.77 LMNA (0.42) LMNAMEN1ALDH1A1HTTKMT2A
SCHEMBL20210214 0.76 TDP1 (0.50) TDP1APEX1PMP22CYP1A2CYP2D6
SCHEMBL12201612 0.76 ADH1B (0.41) TDP1MEN1ALDH1A1KMT2A
SCHEMBL21118983 0.76 LMNA (0.46) LMNAMEN1ALDH1A1HTTKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2005094832-A1 COMPOSITIONS COMPRISING MELOXICAM BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-10-13 WO claimed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US claimed
EP-4748383-A1 OPHTHALMIC COMPOSITION Rohto Pharmaceutical Co., Ltd. (JP) 2026-05-27 EP disclosed
US-20250228887-A1 OPHTHALMIC COMPOSITION ROHTO PHARMACEUTICAL CO., LTD. (JP) 2025-07-17 US disclosed
WO-2025053216-A1 OPHTHALMIC COMPOSITION ロート製薬株式会社 2025-03-13 WO disclosed
WO-2025053197-A1 OPHTHALMIC COMPOSITION ロート製薬株式会社 2025-03-13 WO disclosed
WO-2024262353-A1 COMPOSITION FOR ORAL CAVITY ライオン株式会社 2024-12-26 WO disclosed
US-20240390416-A1 OPHTHALMOLOGICAL COMPOSITION ROHTO PHARMACEUTICAL CO., LTD. (JP) 2024-11-28 US disclosed
EP-4393510-A1 OPHTHALMOLOGICAL COMPOSITION Rohto Pharmaceutical Co., Ltd. (JP) 2024-07-03 EP disclosed
EP-4393496-A1 OPHTHALMIC COMPOSITION Rohto Pharmaceutical Co., Ltd. (JP) 2024-07-03 EP disclosed
US-12005070-B2 Protective agent for keratoconjunctiva or suppressive agent for keratoconjunctival disorder TOYO SUGAR REFINING CO., LTD. (JP) 2024-06-11 US disclosed
EP-0968712-A1 FELBINAC-CONTAINING PATCH Hisamitsu Pharmaceutical Co., Inc. (JP) 2000-01-05 EP disclosed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US disclosed
EP-0665009-A1 CRYSTALLINE CONDITION DISLOCATING METHOD NIPPON SHINYAKU COMPANY, LIMITED (JP) 1995-08-02 EP disclosed
US-5428056-A Terpene amino alcohols and medicinal uses thereof KURARAY CO., LTD. (JP) 1995-06-27 US disclosed
US-5284850-A Antiallergens, improve cerebral function KURARAY CO., LTD. (JP) 1994-02-08 US disclosed
EP-0209158-B1 Terpene amino alcohols and medicinal uses thereof KURARAY CO (JP) 1993-12-08 EP disclosed
US-5143921-A Antiallergens, improving cerebral function KURARAY CO., LTD. (JP) 1992-09-01 US disclosed
US-4946857-A ANTIALLERGENS; IMPROVE CEREBRAL FUNCTION KURARAY CO., LTD. (JP) 1990-08-07 US disclosed
EP-0209158-A2 Terpene amino alcohols and medicinal uses thereof KURARAY CO., LTD. (JP) 1987-01-21 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 (1 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-12005070-B2 Protective agent for keratoconjunctiva or suppressive agent for keratoconjunctival disorder UGCG, GBA1, GOLGA2 LMNA 1761/4885TDP1 3494/4885MEN1 1511/4885

“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.