{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-09-09", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "codes": [ { "uuid": "5f82fae7-7f5e-43ce-9325-7b5834b2c404", "code": "64432-06-0", "type": "PRIMARY", "url": "https://commonchemistry.cas.org/detail?cas_rn=64432-06-0", "code_system": "CAS", "references": [ "0cf3a8c9-9748-4c4c-b9d2-6f1a3af01d6e", "0a755803-3b17-4bee-9abf-3dc7be464138" ] }, { "uuid": "61fe74e9-3836-47f8-af00-83af2fc3bd66", "code": "72941582", "type": "PRIMARY", "url": "https://pubchem.ncbi.nlm.nih.gov/compound/72941582", "code_system": "PUBCHEM", "references": [ "0cf3a8c9-9748-4c4c-b9d2-6f1a3af01d6e" ] }, { "uuid": "38a8d7fc-7793-456e-b44a-096eee05d315", "code": "BV1X94PJ0P", "type": "PRIMARY", "code_system": "FDA UNII" }, { "uuid": "19eb11a8-93de-20d2-b23c-29f874cb7557", "code": "100000182008", "type": "PRIMARY", "code_system": "SMS_ID", "references": [ "51b420a6-eb3b-017c-32bf-225c72f60ae4" ] }, { "uuid": "a90c870d-eb36-c4e5-0a88-24089746aca5", "code": "DTXSID40983005", "type": "PRIMARY", "url": "https://comptox.epa.gov/dashboard/chemical/details/DTXSID40983005", "code_system": "EPA CompTox", "references": [ "0d9d879a-6912-8a87-578a-d69e7a90c9f8" ] } ], "relationships": [ { "uuid": "63a8cb30-d82c-4a15-ab48-60a98372e468", "comments": "Isolated stevia sweetener, produced by the extraction of STEVIA REBAUDIANA leaves by hot water and powdering.", "type": "PARENT->CONSTITUENT ALWAYS PRESENT", "references": [ "6872c228-8ccc-4180-9807-50ff36883e8f" ], "related_substance": { "uuid": "bd9729d1-f8a3-4199-ba60-ea6f7ac2b693", "refuuid": "9de3c1b3-dd78-4d38-9230-990ef6702535", "name": "STEVIA REBAUDIANA LEAF", "unii": "6TC6NN0876", "linking_id": "6TC6NN0876", "ref_pname": "STEVIA REBAUDIANA LEAF", "substance_class": "reference" } } ], "substance_class": "chemical", "names": [ { "uuid": "f1844c11-e70b-4988-995d-ab1bc1b45f3b", "name": "(-)-DULCOSIDE A", "stdName": "(-)-DULCOSIDE A", "type": "cn", "languages": [ "en" ], "preferred": false, "references": [ "fea8a517-9243-4164-8982-95061eb70f19", "1a70f090-e2f3-44a5-b864-600fda0a6985" ], "display_name": false }, { "uuid": "5c981fd2-8302-4ce0-90fe-f76418b09f60", "name": "DUL", "stdName": "DUL", "type": "cn", "languages": [ "en" ], "preferred": false, "references": [ "b872e62b-7719-4b3d-be1c-b4fdbe67f672", "1a70f090-e2f3-44a5-b864-600fda0a6985" ], "display_name": false }, { "uuid": "018f6242-81cc-430e-ad8f-416e0b27fb34", "name": "DULCOSIDE A", "stdName": "DULCOSIDE A", "type": "cn", "languages": [ "en" ], "preferred": false, "references": [ "eff5da30-06aa-4d13-a19d-31df88851a9a", "1a70f090-e2f3-44a5-b864-600fda0a6985" ], "display_name": true }, { "uuid": "198a58f0-73c5-4f75-ac47-d445ceabcecf", "name": "DULCOSIDE A, (-)-", "stdName": "DULCOSIDE A, (-)-", "type": "cn", "languages": [ "en" ], "preferred": false, "references": [ "fea8a517-9243-4164-8982-95061eb70f19", "1a70f090-e2f3-44a5-b864-600fda0a6985" ], "display_name": false }, { "uuid": "f23514ef-5e7e-4b87-9d81-31fe591d3160", "name": "KAUR-16-EN-18-OIC ACID, 13-((2-O-(6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL)-.BETA.-D-GLUCOPYRANOSYL)OXY)-, .BETA.-D-GLUCOPYRANOSYL ESTER, (4.ALPHA.)-", "stdName": "KAUR-16-EN-18-OIC ACID, 13-((2-O-(6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL)-.BETA.-D-GLUCOPYRANOSYL)OXY)-, .BETA.-D-GLUCOPYRANOSYL ESTER, (4.ALPHA.)-", "type": "sys", "languages": [ "en" ], "preferred": false, "references": [ "eff5da30-06aa-4d13-a19d-31df88851a9a", "1a70f090-e2f3-44a5-b864-600fda0a6985" ], "display_name": false } ], "references": [ { "uuid": "fea8a517-9243-4164-8982-95061eb70f19", "citation": "FDA_SRS", "doc_type": "SRS", "public_domain": true, "tags": [ "NOMEN", "PUBLIC_DOMAIN_RELEASE", "AUTO_SELECTED" ] }, { "uuid": "1a70f090-e2f3-44a5-b864-600fda0a6985", "citation": "STN (SCIFINDER)", "doc_type": "STN (SCIFINDER)", "public_domain": true, "tags": [ "NOMEN" ] }, { "uuid": "eff5da30-06aa-4d13-a19d-31df88851a9a", "citation": "STN", "doc_type": "SRS", "public_domain": true, "tags": [ "NOMEN" ] }, { "uuid": "b872e62b-7719-4b3d-be1c-b4fdbe67f672", "citation": "http://www.tandfonline.com/doi/pdf/10.1080/19440049.2013.843101", "url": "http://www.tandfonline.com/doi/pdf/10.1080/19440049.2013.843101", "doc_type": "SRS", "public_domain": true, "tags": [ "NOMEN" ] }, { "uuid": "0cf3a8c9-9748-4c4c-b9d2-6f1a3af01d6e", "citation": "SRS CODE IMPORT", "doc_type": "SRS", "public_domain": true, "document_date": 1493391980000, "tags": [ "NOMEN" ] }, { "uuid": "6872c228-8ccc-4180-9807-50ff36883e8f", "citation": "KAKIGI, Y ET AL, CLASSIFICATION OF STEVIA SWEETENERS IN SOFT DRINKS USING LIQUID CHROMATOGRAPHY AND TIME-OF-FLIGHT MASS SPECTROMETRY, FOOD ADDITIVES & CONTAMINANTS. PART A., 30(12)2043-2049, 2013", "url": "http://www.tandfonline.com/doi/pdf/10.1080/19440049.2013.843101", "doc_type": "JOURNAL ARTICLE", "public_domain": true, "tags": [ "NOMEN" ] }, { "uuid": "d537eee6-9940-4246-8bb2-93bd71be1508", "citation": "SRS import [BV1X94PJ0P]", "url": "http://fdasis.nlm.nih.gov/srs/srsdirect.jsp?regno=BV1X94PJ0P", "doc_type": "SRS", "public_domain": true, "document_date": 1493391980000, "tags": [ "NOMEN" ] }, { "uuid": "0a755803-3b17-4bee-9abf-3dc7be464138", "citation": "STN", "doc_type": "STN (SCIFINDER)", "public_domain": true }, { "uuid": "0d9d879a-6912-8a87-578a-d69e7a90c9f8", "citation": "EPA CompTox", "doc_type": "EPA", "public_domain": true }, { "uuid": "51b420a6-eb3b-017c-32bf-225c72f60ae4", "citation": "EU-SRS", "doc_type": "EMA LIST", "public_domain": true } ], "definition_type": "PRIMARY", "moieties": [ { "uuid": "5d8401b0-6006-4451-a08f-3f85059a194f", "id": "5d8401b0-6006-4451-a08f-3f85059a194f", "molfile": "\n Marvin 01132104512D \n\n 55 61 0 0 1 0 999 V2000\n 8.6362 -4.5929 0.0000 C 0 0 2 0 0 0 0 0 0 2 0 0\n 8.2239 -5.3075 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.4608 -4.5929 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 9.8730 -3.8783 0.0000 C 0 0 1 0 0 0 0 0 0 2 0 0\n 10.6976 -3.8783 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 11.1099 -4.5929 0.0000 C 0 0 2 0 0 0 0 0 0 1 0 0\n 11.9344 -4.5929 0.0000 C 0 0 1 0 0 0 0 0 0 2 0 0\n 12.3467 -3.8783 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 12.3467 -5.3075 0.0000 C 0 0 2 0 0 0 0 0 0 2 0 0\n 13.1713 -5.3075 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 11.9344 -6.0221 0.0000 C 0 0 1 0 0 0 0 0 0 1 0 0\n 12.3467 -6.7367 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.1713 -6.7367 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 11.1099 -6.0221 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 10.6976 -5.3075 0.0000 C 0 0 1 0 0 0 0 0 0 2 0 0\n 9.8730 -5.3075 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 9.4608 -6.0221 0.0000 C 0 0 1 0 0 0 0 0 0 2 0 0\n 8.6637 -6.7367 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.9111 -7.7812 0.0000 C 0 0 2 0 0 0 0 0 0 1 0 0\n 9.6806 -7.4788 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.9280 -6.7093 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.7251 -6.5718 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.9111 -8.6058 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.1964 -9.0181 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.4818 -8.6058 0.0000 C 0 0 2 0 0 0 0 0 0 2 0 0\n 6.7672 -9.0181 0.0000 C 0 0 1 0 0 0 0 0 0 1 0 0\n 6.0525 -9.4303 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.0525 -8.6058 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.0525 -7.7812 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.7672 -7.3689 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.4818 -7.7812 0.0000 C 0 0 2 0 0 0 0 0 0 2 0 0\n 7.4818 -6.9567 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.1964 -7.3689 0.0000 C 0 0 2 0 0 0 0 0 0 1 0 0\n 8.0590 -6.5718 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.6362 -5.9672 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.7672 -9.8426 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.4818 -10.2549 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.0525 -10.2549 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.0525 -11.0795 0.0000 C 0 0 2 0 0 0 0 0 0 2 0 0\n 5.3379 -11.4917 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 5.3379 -12.3163 0.0000 C 0 0 2 0 0 0 0 0 0 1 0 0\n 4.6233 -12.7286 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 3.9087 -12.3163 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.0525 -12.7286 0.0000 C 0 0 1 0 0 0 0 0 0 2 0 0\n 6.0525 -13.5531 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.7672 -12.3163 0.0000 C 0 0 2 0 0 0 0 0 0 2 0 0\n 7.4818 -12.7286 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.7672 -11.4917 0.0000 C 0 0 1 0 0 0 0 0 0 1 0 0\n 7.4818 -11.0795 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 9.4608 -3.1637 0.0000 C 0 0 2 0 0 0 0 0 0 1 0 0\n 9.8730 -2.4490 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 8.6362 -3.1637 0.0000 C 0 0 2 0 0 0 0 0 0 1 0 0\n 8.2239 -2.4490 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 8.2239 -3.8783 0.0000 C 0 0 1 0 0 0 0 0 0 1 0 0\n 7.3993 -3.8783 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 1 2 1 1 0 0 0\n 1 3 1 0 0 0 0\n 54 1 1 0 0 0 0\n 4 3 1 0 0 0 0\n 4 5 1 6 0 0 0\n 50 4 1 0 0 0 0\n 6 5 1 6 0 0 0\n 7 6 1 0 0 0 0\n 6 15 1 0 0 0 0\n 7 8 1 1 0 0 0\n 9 7 1 0 0 0 0\n 9 10 1 6 0 0 0\n 9 11 1 0 0 0 0\n 11 12 1 1 0 0 0\n 11 14 1 0 0 0 0\n 12 13 1 0 0 0 0\n 15 14 1 0 0 0 0\n 15 16 1 1 0 0 0\n 17 16 1 0 0 0 0\n 17 18 1 6 0 0 0\n 21 17 1 0 0 0 0\n 17 35 1 0 0 0 0\n 19 18 1 6 0 0 0\n 19 20 1 0 0 0 0\n 19 23 1 0 0 0 0\n 33 19 1 0 0 0 0\n 20 21 1 0 0 0 0\n 22 21 2 0 0 0 0\n 24 23 1 0 0 0 0\n 25 24 1 6 0 0 0\n 25 26 1 0 0 0 0\n 25 31 1 0 0 0 0\n 26 27 1 1 0 0 0\n 26 28 1 0 0 0 0\n 26 36 1 0 0 0 0\n 28 29 1 0 0 0 0\n 29 30 1 0 0 0 0\n 31 30 1 0 0 0 0\n 31 32 1 6 0 0 0\n 31 33 1 0 0 0 0\n 33 34 1 6 0 0 0\n 35 34 1 0 0 0 0\n 36 37 2 0 0 0 0\n 36 38 1 0 0 0 0\n 39 38 1 1 0 0 0\n 39 40 1 0 0 0 0\n 48 39 1 0 0 0 0\n 41 40 1 0 0 0 0\n 41 42 1 1 0 0 0\n 44 41 1 0 0 0 0\n 42 43 1 0 0 0 0\n 44 45 1 6 0 0 0\n 46 44 1 0 0 0 0\n 46 47 1 1 0 0 0\n 48 46 1 0 0 0 0\n 48 49 1 6 0 0 0\n 50 51 1 1 0 0 0\n 52 50 1 0 0 0 0\n 52 53 1 1 0 0 0\n 54 52 1 0 0 0 0\n 54 55 1 6 0 0 0\nM END", "smiles": "C=C1C[C@]23CC[C@H]4[C@@](C)(CCC[C@@]4(C)C(=O)O[C@H]5[C@@H]([C@H]([C@@H]([C@@H](CO)O5)O)O)O)[C@@H]3CC[C@@]1(C2)O[C@H]6[C@@H]([C@H]([C@@H]([C@@H](CO)O6)O)O)O[C@H]7[C@@H]([C@@H]([C@H]([C@H](C)O7)O)O)O", "formula": "C38H60O17", "atropisomerism": "No", "charge": 0, "count": 1, "stereochemistry": "ABSOLUTE", "count_amount": { "type": "MOL RATIO", "average": 1, "units": "MOL RATIO", "uuid": "cb210b97-2fe6-4e14-872f-deac1d9c6b98" }, "defined_stereo": 21, "ez_centers": 0, "molecular_weight": "788.8743", "optical_activity": "UNSPECIFIED", "stereo_centers": 21 } ], "definition_level": "COMPLETE", "uuid": "b7f3a87d-b914-463d-b274-db4cded0aa4c", "version": "7", "structure": { "id": "63a5e3db-4b76-4311-8509-d8380cb3078b", "molfile": "\n Marvin 01132105112D \n\n 57 63 0 0 1 0 999 V2000\n 10.7251 -6.5718 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.9280 -6.7093 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.6806 -7.4788 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.9111 -7.7812 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\n 8.9111 -8.6058 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.1964 -9.0181 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.4818 -8.6058 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 6.7672 -9.0181 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\n 6.0525 -8.6058 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.0525 -7.7812 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.7672 -7.3689 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.4818 -7.7812 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\n 8.1964 -7.3689 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 8.1964 -8.1935 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0\n 8.0590 -6.5718 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.6362 -5.9672 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.4608 -6.0221 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 8.6637 -6.7367 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.8730 -5.3075 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 10.6976 -5.3075 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\n 11.1099 -4.5929 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 10.6976 -3.8783 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 9.8730 -3.8783 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\n 9.4608 -3.1637 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 9.8730 -2.4490 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 8.6362 -3.1637 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 8.2239 -2.4490 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 8.2239 -3.8783 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\n 7.3993 -3.8783 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 8.6362 -4.5929 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\n 9.4608 -4.5929 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 8.2239 -5.3075 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.9344 -4.5929 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\n 12.3467 -3.8783 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 12.3467 -5.3075 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 13.1713 -5.3075 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 11.9344 -6.0221 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 11.1099 -6.0221 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 12.3467 -6.7367 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.1713 -6.7367 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 7.4818 -6.9567 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.7672 -9.8426 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.4818 -10.2549 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.0525 -10.2549 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.0525 -11.0795 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\n 6.7672 -11.4917 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 7.4818 -11.0795 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.7672 -12.3163 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\n 7.4818 -12.7286 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.0525 -12.7286 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 6.0525 -13.5531 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 5.3379 -12.3163 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\n 5.3379 -11.4917 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 4.6233 -12.7286 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 3.9087 -12.3163 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 6.0525 -9.4303 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.4818 -9.4303 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0\n 1 2 2 0 0 0 0\n 3 2 1 0 0 0 0\n 4 3 1 0 0 0 0\n 5 4 1 0 0 0 0\n 6 5 1 0 0 0 0\n 7 6 1 0 0 0 0\n 8 7 1 0 0 0 0\n 9 8 1 0 0 0 0\n 9 10 1 0 0 0 0\n 10 11 1 0 0 0 0\n 11 12 1 0 0 0 0\n 7 12 1 0 0 0 0\n 4 13 1 0 0 0 0\n 13 12 1 0 0 0 0\n 13 14 1 1 0 0 0\n 13 15 1 0 0 0 0\n 16 15 1 0 0 0 0\n 2 17 1 0 0 0 0\n 17 16 1 0 0 0 0\n 17 18 1 6 0 0 0\n 4 18 1 6 0 0 0\n 17 19 1 0 0 0 0\n 20 19 1 1 0 0 0\n 20 21 1 0 0 0 0\n 21 22 1 6 0 0 0\n 23 22 1 6 0 0 0\n 23 24 1 0 0 0 0\n 24 25 1 1 0 0 0\n 24 26 1 0 0 0 0\n 26 27 1 1 0 0 0\n 26 28 1 0 0 0 0\n 28 29 1 6 0 0 0\n 28 30 1 0 0 0 0\n 30 31 1 0 0 0 0\n 23 31 1 0 0 0 0\n 30 32 1 1 0 0 0\n 21 33 1 0 0 0 0\n 33 34 1 1 0 0 0\n 33 35 1 0 0 0 0\n 35 36 1 6 0 0 0\n 35 37 1 0 0 0 0\n 37 38 1 0 0 0 0\n 20 38 1 0 0 0 0\n 37 39 1 1 0 0 0\n 39 40 1 0 0 0 0\n 12 41 1 6 0 0 0\n 8 42 1 0 0 0 0\n 42 43 2 0 0 0 0\n 42 44 1 0 0 0 0\n 45 44 1 1 0 0 0\n 45 46 1 0 0 0 0\n 46 47 1 6 0 0 0\n 46 48 1 0 0 0 0\n 48 49 1 1 0 0 0\n 48 50 1 0 0 0 0\n 50 51 1 6 0 0 0\n 50 52 1 0 0 0 0\n 52 53 1 0 0 0 0\n 45 53 1 0 0 0 0\n 52 54 1 1 0 0 0\n 54 55 1 0 0 0 0\n 8 56 1 1 0 0 0\n 7 57 1 1 0 0 0\nM END", "smiles": "C=C1C[C@]23CC[C@@]4([H])[C@@](C)(CCC[C@@]4(C)C(=O)O[C@H]5[C@@H]([C@H]([C@@H]([C@@H](CO)O5)O)O)O)[C@]3([H])CC[C@@]1(C2)O[C@H]6[C@@H]([C@H]([C@@H]([C@@H](CO)O6)O)O)O[C@H]7[C@@H]([C@@H]([C@H]([C@H](C)O7)O)O)O", "formula": "C38H60O17", "atropisomerism": "No", "charge": 0, "count": 1, "stereochemistry": "ABSOLUTE", "defined_stereo": 21, "ez_centers": 0, "molecular_weight": "788.8743", "optical_activity": "UNSPECIFIED", "references": [ "eff5da30-06aa-4d13-a19d-31df88851a9a", "d537eee6-9940-4246-8bb2-93bd71be1508" ], "stereo_centers": 21 }, "unii": "BV1X94PJ0P" } ] }