Indinavir Anhydrous

Indinavir Anhydrous

SCHEMBL6317

CC(C)(C)NC(=O)[C@@H]1CN(Cc2cccnc2)CCN1C[C@@H](O)C[C@@H](Cc1ccccc1)C(=O)N[C@H]1c2ccccc2C[C@H]1O

nearest known ligand 0.99

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 18/20 0.99
ABCC3 O15438 1/20 0.99
ABCB11 O95342 1/20 0.99
ABCB1 P08183 1/20 0.99
TACR2 P21452 1/20 0.99
TBXAS1 P24557 1/20 0.99
SLC47A2 Q86VL8 1/20 0.99
SLC47A1 Q96FL8 1/20 0.99
NR1I2 O75469 1/20 0.95
LMNA P02545 1/20 0.95
CYP2D6 P10635 13/20 0.75
CYP2C9 P11712 6/20 0.55

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
Indinavir Anhydrous SCHEMBL1176257 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL7752012 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL19760130 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL13039789 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL20099152 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL17787450 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL6908581 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL19460567 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL21683359 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2
Indinavir Anhydrous SCHEMBL21578565 1.00 CYP3A4 (0.99) CYP3A4ABCC3ABCB11ABCB1TACR2

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

Appears in 47886 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026107113-A1 MODIFIED CELLS FOR PROGRAMMING EXTRA ENVELOPED VIRUSES (EEVs) AND THEIR USE FOR PRODUCING THE EEVs, THE PROGRAMMED EEVs AND USES THEREOF CALIDI BIOTHERAPEUTICS (NEVADA), INC. (US) 2026-05-21 WO claimed
US-20260139860-A1 PRODUCTS OF MANUFACTURE FOR THE TREATMENT, PREVENTION AND AMELIORATION OF MICROBIAL INFECTIONS CENTRE FOR DIGESTIVE DISEASES (AU) 2026-05-21 US claimed
EP-4744729-A2 METHODS OF TREATING GASTROINTESTINAL STROMAL TUMORS Deciphera Pharmaceuticals, LLC (US) 2026-05-20 EP claimed
EP-4094767-B1 NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS AND USES RELATED THERETO UNIV EMORY (US) 2026-05-20 EP claimed
US-12629363-B2 Prophylaxis and treatment of angioedema PHARVARIS GMBH (CH) 2026-05-19 US claimed
US-20260124290-A1 HIV Immunogens, Vaccines, and Methods Related Thereto UNIV EMORY (US) 2026-05-07 US claimed
EP-4255391-B1 LUMINOL FOR USE IN THE TREATMENT OF SEQUELAE OF A SARS-COV-2 INFECTION METRIOPHARM AG (CH) 2026-05-06 EP claimed
WO-2026085583-A1 MOLECULAR ASSAY FOR DETECTING HIV-1 DRUG-RESISTANT MUTATIONS ST VINCENT'S HOSPITAL SYDNEY LIMITED (AU) 2026-04-30 WO claimed
WO-2026086804-A1 MULTILAYER-REGULATED GENE EDITING SYSTEM AND USE THEREOF 自如基因科技(深圳)有限公司 2026-04-30 WO claimed
EP-4731611-A1 TARGETED DEGRADERS OF HIV-1 NEF FOR THE TREATMENT OF HIV DISEASE UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2026-04-29 EP claimed
WO-1998017282-A1 METHODS OF USING SUCROSE OCTASULFATE TO TREAT OR PREVENT ENVELOPED VIRUS INFECTION VERTEX PHARMACEUTICALS INCORPORATED (US) 1998-04-30 WO claimed
WO-1998014436-A1 4,4-DISUBSTITUTED-1,4-DIHYDRO-2H-3,1-BENZOXAZIN-2-ONES USEFUL AS HIV REVERSE TRANSCRIPTASE INHIBITORS AND INTERMEDIATES AND PROCESSES FOR MAKING THE SAME DUPONT PHARMACEUTICALS COMPANY (US) 1998-04-09 WO claimed
WO-1998004290-A2 COMPOSITIONS COMPRISING AN INDUCING AGENT AND AN ANTI-VIRAL AGENT FOR THE TREATMENT OF BLOOD, VIRAL AND CELLULAR DISORDERS PERRINE SUSAN P (US) 1998-02-05 WO claimed
WO-1997042962-A1 FORMULATION FOR USE IN THE PREVENTION OF PATHOGEN INDUCED DISEASES INCLUDING HIV AND HSV BERGERON MICHEL G (CA) 1997-11-20 WO claimed
WO-1997029751-A1 USE OF LEUKOTRIENE B4 OR ITS ANALOGUES AS ANTIVIRAL AND ANTINEOPLASTIC AGENTS VIROCELL INC. (CA) 1997-08-21 WO claimed
WO-1997027180-A1 ASPARTYL PROTEASE INHIBITORS VERTEX PHARMACEUTICALS INCORPORATED (US) 1997-07-31 WO claimed
WO-1997027480-A1 METHOD OF MANAGING THE CHEMOTHERAPY OF PATIENTS WHO ARE HIV POSITIVE BASED ON THE PHENOTYPIC DRUG SENSITIVITY OF HUMAN HIV STRAINS VIRCO N.V. (BE) 1997-07-31 WO claimed
WO-1997021683-A1 RETROVIRAL PROTEASE INHIBITING COMPOUNDS ABBOTT LABORATORIES (US) 1997-06-19 WO claimed
WO-1997021685-A1 RETROVIRAL PROTEASE INHIBITING COMPOUNDS ABBOTT LABORATORIES (US) 1997-06-19 WO claimed
CN-1132756-A Antiviral ethers of aspartate protease substrate isosteres CIBA GEIGY AG (CH) 1996-10-09 CN claimed